Reproductive health research in Australia and New Zealand: highlights from the Annual Meeting of the Society for Reproductive Biology, 2019
Amy Winship A , Jacqueline Donoghue B , Brendan J. Houston C , Jacinta H. Martin D , Tessa Lord D E , Alaknanda Adwal F , Macarena Gonzalez F , Elodie Desroziers G H , Gulfam Ahmad I , Dulama Richani J and Elizabeth G. Bromfield![https://orcid.org/0000-0001-7256-1403](/media/client/orcid_16x16.png)
A Biomedicine Discovery Institute, Department of Anatomy and Developmental Biology, Stem Cells and Development Program, Monash University, 19 Innovation Walk, Clayton, Vic. 3800, Australia.
B The University of Melbourne, Department of Obstetrics and Gynaecology, Gynaecology Research Centre, Royal Women’s Hospital, 20 Flemington Rd, Parkville, Vic. 3052, Australia.
C School of Biological Sciences, Monash University, 25 Rainforest Walk, Clayton, Vic. 3800, Australia.
D Hunter Medical Research Institute, Pregnancy and Reproduction Program, Lot 1 Kookaburra Cct, New Lambton Heights, NSW 2305, Australia.
E Priority Research Centre for Reproductive Science, Discipline of Biological Sciences, The University of Newcastle, Callaghan, NSW 2300, Australia.
F School of Medicine, Robinson Research Institute, The University of Adelaide, Adelaide, SA 5005, Australia.
G Department of Physiology, University of Otago, PO Box 56, Dunedin 9054, New Zealand.
H Centre for Neuroendocrinology, University of Otago, PO Box 913, Dunedin 9054, New Zealand.
I The University of Sydney Medical School, Discipline of Pathology, School of Medical Sciences, Sydney, NSW 2006, Australia.
J School of Women’s and Children’s Health, Fertility & Research Centre, University of New South Wales Medicine, Sydney, NSW 2052 Australia.
K Department of Biochemistry and Cell Biology, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 1, 3584 CL Utrecht, Netherlands.
L Corresponding author: Elizabeth.bromfield@newcastle.edu.au
Reproduction, Fertility and Development 32(7) 637-647 https://doi.org/10.1071/RD19449
Submitted: 9 December 2019 Accepted: 13 December 2019 Published: 1 April 2020
Journal Compilation © CSIRO 2020 Open Access CC BY-NC-ND
Abstract
The 2019 meeting of the Society for Reproductive Biology (SRB) provided a platform for the dissemination of new knowledge and innovations to improve reproductive health in humans, enhance animal breeding efficiency and understand the effect of the environment on reproductive processes. The effects of environment and lifestyle on fertility and animal behaviour are emerging as the most important modern issues facing reproductive health. Here, we summarise key highlights from recent work on endocrine-disrupting chemicals and diet- and lifestyle-induced metabolic changes and how these factors affect reproduction. This is particularly important to discuss in the context of potential effects on the reproductive potential that may be imparted to future generations of humans and animals. In addition to key summaries of new work in the male and female reproductive tract and on the health of the placenta, for the first time the SRB meeting included a workshop on endometriosis. This was an important opportunity for researchers, healthcare professionals and patient advocates to unite and provide critical updates on efforts to reduce the effect of this chronic disease and to improve the welfare of the women it affects. These new findings and directions are captured in this review.
![Graphical Abstract Image](/temp/RD19449_toc.jpg)
Introduction
Our health during adulthood begins as early as fertilisation and time in the womb. Therefore, understanding the crucial factors governing reproductive health underlies our ability to improve the health of future generations. Leveraging this fundamental knowledge can open doors for the design of new diagnostic tools, therapeutics and intervention measures. However, after the 2019 Society for Reproductive Biology (SRB) Meeting, we understand more than ever that partnering this knowledge with diverse, cross-disciplinary teams is key to us ultimately improving reproductive outcomes, as a community. We saw numerous examples of collaborations between scientists, clinicians, engineers, bioinformaticians and mathematicians teaming up to advance reproductive health through revolutionary new approaches and technologies. This summary of the 2019 Annual Meeting highlights the novel advances being made to address topical reproductive health issues ranging from endometriosis and the improvement of assisted reproductive techniques (ARTs) to synthesising big data and understanding the effect of the environment on reproductive health. Importantly, the partnerships being forged to facilitate these advances are outlined in this review.
Inaugural SRB endometriosis workshop
Participating speakers: Linda Giudice, Susan Evans, Stuart Brierley, Caitlin Filby, Gita Mishra, Peter Rogers, Melissa Parker, Sally Mortlock, Sarah Holdsworth-Carson
The inaugural SRB endometriosis workshop, Australian Endometriosis Research: The State of the Art and What the Future Looks Like, was held as a satellite meeting in conjunction with the SRB Annual Scientific Meeting in Sydney at The Royal Hospital for Women. The meeting was co-organised by Louise Hull, Sarah Holdsworth-Carson, Jane Girling and Jason Abbott, bringing together scientists, clinicians and patient advocates from around Australia and New Zealand to showcase current research activities and updates.
Endometriosis is a chronic, inflammatory, oestrogen-dependent disease that affects an estimated 176 million women globally and is the leading cause of infertility. With a personal cost of nearly A$30 000 and an economic burden of A$9.6 billion each year in Australia (Armour et al. 2019), new clinical, basic science and government initiatives are needed to improve this situation. Peter Rogers (The University of Melbourne) and Cecilia Ng (Jean Hailes) were invited to provide an update about the National Action Plan for Endometriosis (NAPE, https://www1.health.gov.au/internet/main/publishing.nsf/Content/endometriosis, accessed 1 October 2019). After years of identifying the unmet needs and research priorities for endometriosis (Horne et al. 2017; Rogers et al. 2017; As-Sanie et al. 2019) and consumer-driven advocacy of federal politicians, the Parliamentary Friends of Endometriosis Awareness group was established to push for a policy response to address the disease. In early 2018, a National Round Table was held where patients, advocates, clinicians, scientists and government officials commenced development of the NAPE. Following a national consultation process, the final document was established that outlined three key areas requiring federal support: (1) awareness; (2) clinical management; and (3) research with measurable outcomes to include improved quality of life and a reduction in the effect of endometriosis on the individual and the community.
To date, the NAPE has delivered a total of A$15 million, with A$2.5 million towards the founding of a National Endometriosis Clinical and Scientific Trials (NECST) network that has engaged VCS Digital Health to build and integrate demographic, clinical outcomes, imaging, Patient Reported Outcome Measures (PROMS), and biobank information from endometriosis patients from across Australia. A further A$3.4 million has been allocated for the development of education and clinical guidelines, digital health and online patient advocacy platforms, and there is a Medical Research Future Fund targeted call for Endometriosis Research worth A$9 million. Within 5 years, the NAPE is expected to deliver significant improvements in patient diagnosis, treatment and quality of life. As part of developing the NAPE, a clearer picture of how many women experienced endometriosis in Australia was required. Gita Mishra (Director, Australian Longitudinal Study of Women’s Health (ALSWH), University of Queensland), presented new data on the prevalence of endometriosis in Australia. Using data from ALSWH, Professor Mishra highlighted that endometriosis needs to be identified as a chronic disease because it exhibits prevalence rates higher than vascular disease (4.8%), type 2 diabetes (5%) and asthma (11.2%).
Endometriosis-related pain was a key topic of the day. Endometriosis research updates were opened by Linda Giudice from University of California San Francisco who was awarded the SRB Founder’s Oration and Medal Lecture 2019. Professor Giudice presented an overview of endometriosis pathogenesis theories, including genetic, epigenetic and environmental factors, with a focus on the role of endocrine disruptors in the establishment of endometriosis through modulation of the epigenome. Of interest was the indication that endocrine disruptors such as dioxin induce transgenerational epigenome disruption (Manikkam et al. 2012; Nilsson et al. 2018). These findings suggest that maternal exposure to dioxin could alter the embryonic epigenome by altering methylation patterns of imprinted genes, resulting in adverse effects in subsequent generations. Although rodent and non-human primates have been used to demonstrate the role of dioxin in the establishment of endometriosis (Rier and Foster 2002), evidence linking dioxin exposure to endometriosis development in humans is limited (Simsa et al. 2010).
Research into the most debilitating consequence of endometriosis, chronic pelvic pain (CPP), was then discussed. Melissa Parker (Canberra Endometriosis Centre) described her latest research, which evaluated the effect of menstrual disturbance, including period pain, on adolescent health. This reflected data from a second cohort of 1000 15- to 19-year-old females who completed the Menstrual Disorder of Teenagers (MDOT) and Period ImPact and Pain Assessment (PIPPA) surveys. These data identified significant menstrual disturbance in 25% of girls surveyed, with the pain causing disruption in daily activities and increased absenteeism from both school and work. The PIPPA survey is currently being developed as an online resource to facilitate self-screening for menstrual disturbance using PIPPA and education about managing period pain, first-line measures and when to seek primary health care. The website aims to help young women determine what is normal or not for menstrual periods and open constructive supportive dialogue with their carers about period pain.
Susan Evans (Pelvic Pain Foundation of Australia) then provided an overview of how we describe CPP in order to improve clinical understanding of pain syndromes and treatment. Dr Evans presented research about the comorbidities of dysmenorrhoea, stating that stabbing pain in association with endometriosis was highly associated with dysmenorrhoea severity, length of menstruation and pelvic and extrapelvic pain (Evans et al. 2018). The research also highlighted that symptoms associated with dysmenorrhoea can be independent of endometriosis and hormone use. This finding further supported the notion that CPP and endometriosis may be independent conditions that coexist, requiring treatment options suited to each condition. To round out the discussion on pain, Stuart Brierley (Flinders University and South Australian Health and Medical Research Institute) presented an overview of the neural pathways underlying abdominal and pelvic pain (Grundy et al. 2019), including the description of neuronal cross-organ sensitisation between the bowel, bladder and vagina. This overview also included details of a recent preclinical study describing how a gut-acting therapy like linaclotide (a synthetic guanylate cyclase 2C agonist, currently clinically approved for use in irritable bowel syndrome patients with constipation) reduced comorbid CPP in rodent models of endometriosis (Ge et al. 2019).
To finalise the day, several researchers provided updates on the phenotypes, risks and potential causes of endometriosis. Sally Mortlock (Queensland University) provided an update on the endometriosis genome-wide association studies (GWAS) research that, to date, has identified 19 independent single nucleotide polymorphisms (SNPs) at 14 distinct genomic loci associated with endometriosis risk (Fung and Montgomery 2018). Dr Mortlock also discussed recent research investigating the epigenome and methylation signatures of endometriosis patients (Mortlock et al. 2019). From her study, 4546 sentinel cis-methylation quantitative trait loci were identified, with one located in the endometriosis risk region near the growth regulating estrogen receptor binding 1 (GREB1) gene. Expansion of her research will involve the inclusion of patient phenotypic information (age, body mass index (BMI), pain, day of cycle) and cell-specific features (endometrial epithelium and stroma) to determine risk SNPs and genes related to endometriosis phenotypes. Sarah Holdsworth-Carson (The University of Melbourne) presented recent data on the heterogeneity of endometriotic lesions. Using pathology specimens and investigating microscopic cellular features, little correlation was observed between cell characteristics and patient clinical information (e.g. duration of symptoms or cycle stage). Dr Holdsworth-Carson also presented novel research investigating the spatial distribution of metabolites, proteins and N-glycans in endometriotic lesions, with early data also indicating significant heterogeneity between lesions and eutopic endometrium. From these findings, the future use of lesion descriptors and application of molecular markers as biomarkers of disease will need to consider overall lesion heterogeneity in order to be effective. Caitlin Filby (Hudson Institute of Medical Research) provided an update on the most recent research on the cellular origins of endometriosis (Valentijn et al. 2013; Gargett et al. 2014; Nguyen et al. 2017; Cousins et al. 2018), including investigation of the presence of endometrial stem and progenitor cells in peritoneal fluid and menstrual blood. This work was discussed in the context of recent publications on cancer-associated somatic mutations in the epithelial cells of deep infiltrating endometriotic lesions (Anglesio et al. 2015; Anglesio and Yong 2017; Suda et al. 2018) and advances in endometrial organoid technology (Boretto et al. 2017, 2019; Turco et al. 2017). Importantly, the ability to generate organoids from the lesions themselves is a major advance that is likely to aid our understanding of how endometriosis lesions form and how best to treat them using a personalised medicine approach.
The symposium was closed with a panel discussion including Grant Montgomery (University of Queensland), Caroline Gargett (Hudson Institute of Medical Research), Louise Hull, Cecilia Ng and Peter Rogers and moderated by Jane Girling highlighting the need for personalised treatment, novel screening and diagnostic tools, increasing the collection of patient phenotypic data, more multidisciplinary collaborations and increasing education and outreach opportunities to communities that are hindered by language, culture and location. By implementing the key findings of the panel discussion and aligning research to endometriosis patient needs, researchers are certain to make significant contributions to improving the lives of endometriosis patients in the coming years:
Keep small successes going so larger successes can be achieved. [Linda Giudice, 2019]
Environmental effect on reproduction
Speakers: Bob Wong, Andrew Pask, Nicole McPherson
Environmental variables, both exogenous and endogenous, can modulate the behaviour and homeostasis of living organisms. Such variables are not only limited to physical, chemical and biological factors, but include lifestyle, diet and hormones (Bhargava et al. 2017). Across time, organisms and populations have continually adapted to changing environmental stresses and conditions. But unarguably the past few decades have brought an unprecedented rate and magnitude of detrimental changes in many ecosystems, exacerbated by human activities such as increasing chemical and pharmaceutical pollution, greenhouse gases and deforestation. These factors have drastically altered not only the natural habitats of many native species, but also their behaviour responses, development and reproduction. For example, 17β-trenbolone, a highly potent endocrine disruptor with androgen-mimicking activity, is commonly used as a hormonal growth promoter in the beef industry (Lagesson et al. 2019). This chemical enters aquatic ecosystems via livestock effluent run-off and alters the course of reproduction and sexual selection in freshwater fish. Thus, its capacity to alter behaviour in wildlife is a growing environmental concern. For example, in the guppy Poecilia reticulata, males exposed to 17β-trenbolone are frequently more aggressive towards rival males than their unexposed male counterparts (Tomkins et al. 2016). Exposed males also exhibit altered sexual behaviour, such as a decrease in courting behaviour and more sneak (i.e. coercive) mating attempts towards females. Similarly, female guppies exposed to 17β-trenbolone show altered sexual responsiveness and are less discerning in their mate selection (Tomkins et al. 2016).
Another class of endocrine-disrupting chemicals (EDCs) mimics oestrogen and has strong potential to alter downstream endocrine functions, affecting male and female reproduction. The effect of EDCs is not limited to parental reproduction; their transgenerational effects on reproductive organs are also a major concern (Jeng 2014). Sustained or abnormal production of endogenous oestrogen can lead to cancers of reproductive organs, of which endometrial type I carcinoma (Yang et al. 2019) and cervical carcinomas (Chung et al. 2010) are common examples. Increasing exposure to EDCs has affected oestrogen signalling, which has not only been associated with reduced male fertility in terms of functional semen parameters (Rehman et al. 2018), but also resulted in developmental anomalies of the male reproductive tract (Bouty et al. 2015). Among such anomalies, hypospadias is one common condition reported to be higher in males born to mothers having been exposed to oestrogenic EDCs during pregnancy. This anomaly is represented by ectopic placement of the urethral opening and affects 1 in 125 live male births in developed countries (Paulozzi et al. 1997). However, the mechanism by which oestrogen-like EDCs cause hypospadias is not fully understood. Recently, altered expression in urethral patterning and keratin genes were reported in response to compromised oestrogen signalling in mice (Cripps et al. 2019). Notably, a loss of oestrogen signalling in mice deficient in the oestrogen receptor ERα also leads to mild hypospadias (Govers et al. 2019). A similar phenotype has been reported in aromatase (Cyp19α1)-knockout mice (Cripps et al. 2019), which show complete ablation of endogenous oestrogen. These findings indicate that physiological levels of oestrogen are necessary for normal closure of the penile urethra. Nonetheless, the rise in developmental anomalies of the male reproductive tract may be attributed to continuous and increased exposure to exogenous (contraceptive pill, oestrogen-replacement therapies, intrauterine contraceptive devices, oestrogen-rich products) or endogenous (oestrogen-secreting tumours or obesity) oestrogen.
Among endogenous factors, obesity in reproductive-age men is of great concern, because obesity rates have nearly tripled worldwide in the past 30 years and nearly one-quarter of all men are obese (Palmer et al. 2012). This coincides with an increase in male subfertility and infertility, evidenced by the increase in time to natural conception and the number of obese couples seeking ARTs. Numerous studies have demonstrated that male obesity and high BMI are associated with impaired sex steroid hormone production, reduced sperm quality and quantity, increased oxidative sperm DNA damage and changes in the epigenetic status of spermatozoa (McPherson and Lane 2015). However, a growing number of studies also demonstrate that higher adiposity and male obesity are associated with comorbidities, including metabolic syndrome, hypercholesterolaemia, hyperleptinaemia and a proinflammatory state, all of which are independently associated with male subfertility (for a review, see McPherson and Lane 2015). It remains unclear whether increased adiposity is the sole driver of impaired reproductive function in obese males or whether comorbidities also affect sperm quality, quantity and DNA integrity. In a rodent model of male obesity, both diet and exercise interventions improved sperm function (motility, DNA damage, reactive oxygen species (ROS) and mitochondrial function; Palmer et al. 2012). Interestingly, there was no change in adiposity levels in the exercise intervention relative to control group, but exercise did lead to improved glucose function, implicating metabolic dysfunction independent of increased adiposity as a causative factor in impaired sperm function (Palmer et al. 2012).
In humans, the effects of obesity or high BMI on semen parameters and male fertility are inconclusive (for a review, see Palmer et al. 2012). Some argue that increased fat mass is not a robust indicator of subfertility and report no change in sperm concentration (Pauli et al. 2008; Shayeb et al. 2011), whereas others have shown decreased sperm concentration in men with a high BMI (Stewart et al. 2009; Alshahrani et al. 2016). These findings further highlight that, in humans, adiposity alone is likely not the sole determinant of impaired sperm function ascribed to male obesity. Moreover, the correlation between the level of adiposity and BMI can vary between individuals, and does not always take into account differences in muscle mass, blood profile and other metabolic parameters; in time, these may prove to be more reliable indicators of subfertility and allow treatments to be tailored to each patient.
Together, these findings highlight that anthropogenic changes can have both blatant and subtle effects on natural populations. Lifestyle, extensive use of and thus continuous exposure to EDCs negatively affect reproductive capacity, and EDCs also carry potential consequences of transgenerational reproductive anomalies in animals and humans. Therefore, it is vital to understand and assess how organisms will cope in an increasingly human-dominated world, to forecast the likely fate of species in the longer term and, where possible, take the remedial actions necessary to counter the loss of biodiversity and minimise the unwanted effects.
Novel insights into implantation and embryo development
Speakers: Evdokia Dimitriadis, Alexandra Harvey
The intricacies of the implantation process have mystified scientists for years, such that our understanding of this critical phase of development remains virtually unchanged over the past decade. In addition to the requisite synchrony between a receptive endometrium and a good-quality blastocyst (Koot et al. 2012), our understanding of implantation reflects only the broader morphogenetic events of blastocyst apposition, attachment and invasion. This has hindered attempts to resolve the developmental origin and molecular aetiology of implantation failure, a leading contributor to infertility, affecting approximately 15% of all pregnancies worldwide (Zinaman et al. 1996; Koot et al. 2012). It therefore remains difficult to accurately identify and diagnose women at risk of experiencing this condition (Tan et al. 2005; Ford and Schust 2009; Simon and Laufer 2012; Coughlan et al. 2014). Indeed, current therapeutic strategies rely almost exclusively on embryo selection based on morphological criteria and the kinetics of cell division during early embryogenesis (Meseguer et al. 2011). However, neither parameter has proven sufficient to accurately predict embryo implantation potential or pregnancy success. To address this, our speakers spearhead research into novel prognostic biomarkers to predict implantation potential and endometrial receptivity with the goal to improve ARTs.
One such strategy has been to explore the role and predictive capacity of embryo-borne non-coding RNAs (i.e. microRNAs (miRNAs)) in regulating endometrial receptivity (Cuman et al. 2015; Winship et al. 2018). This is perhaps not surprising because miRNAs mediate gene silencing by targeting protein-coding transcripts for degradation and, despite strict temporal and spatial control, dysgenesis of miRNAs is associated with numerous pathological processes, including in reproduction (AbdelHafez et al. 2010; Revel et al. 2011; Zhao et al. 2012; Dior et al. 2014; Ha and Kim 2014; Kropp et al. 2014; Rosenbluth et al. 2014; Cuman et al. 2015). In this context, the study of Cuman et al. (2015) reported that the miRNA profile derived from spent blastocyst media collected from an IVF clinic can be stratified based on implantation success. One miRNA in particular, miR-661, was detected exclusively in the media of embryos with reduced implantation potential; miR-661 has since been shown to be taken up by endometrial cells, where it significantly downregulates gene and protein production of poliovirus receptor-related 1 (PVRL1; also known as Nectin-1) leading to the inhibition of endometrial cell adhesiveness, as determined by a trophoblast spheroid attachment assay (Cuman et al. 2015). Fittingly, nectins have previously been shown to mediate crucial embryo implantation processes (Norwitz et al. 2001; Takai and Nakanishi 2003; Takai et al. 2003, 2008). In addition, a more recent study suggests that miR-661 may also downregulate mouse double minute homologue 2 (MDM2), similarly reducing endometrial epithelial cell adhesion (Winship et al. 2018). These data demonstrate that blastocyst-borne miRNAs actively participate in the implantation process; moreover, the disparity between miRNA profiles from implanting and non-implanting blastocysts may form an intriguing new avenue for their use as biomarkers of implantation potential or as targets to treat implantation failure and infertility.
Another novel strategy with significant potential to increase our understanding of this critical window of early development is the study of embryonic stem cells (ESCs). ESCs represent an important tool to study the molecular biology of the inner cell mass (ICM), established during the first lineage specification event before implantation. The ICM is defined by its pluripotent state and open chromatin structure, and will later give rise to all embryo tissues (Morris et al. 2012; Niakan et al. 2012). Consequently, all cells inherit the epigenetic information established during early lineage specification events, which has recently been shown to be regulated by the external nutrient environment (Moussaieff et al. 2015; Harvey et al. 2016a, 2016b), placing nutrient availability and cellular metabolism at the forefront of developmental regulation. The metabolic fingerprint of the blastocyst is characterised by glycolysis to support the formation and maintenance of the blastocoel cavity and provide biosynthetic precursors for proliferation (Gardner et al. 2011; Gardner and Wale 2013; Gardner and Harvey 2015). Similarly, ESCs rely on glycolytic metabolism to support ongoing proliferation (Zhang et al. 2011; Folmes et al. 2012; Lees et al. 2015; Gu et al. 2016; Harvey et al. 2016a, 2016b).
Despite significant evidence that nutrient availability affects embryo development, viability and differentiation spanning more than three decades (Gardner and Leese 1987; Lane and Gardner 1996; Harvey et al. 2004; Gardner et al. 2011), it remains underappreciated that in vitro embryo culture systems need to closely mimic the physiological environment of the female tract, especially regarding oxygen and nutritional conditions (Gardner 2016; Gardner and Schoolcraft 1999; Gardner et al. 2002). This requirement is also not taken into consideration during the culture of human pluripotent stem cells (PSCs), which can dramatically affect their physiology (for a review, see Lees et al. 2017) and subsequent differentiation capacity (Moussaieff et al. 2015; Shyh-Chang and Daley 2015). Changes in oxygen tension alone modulate human ESC metabolism, epigenetics and differentiation (Lees et al. 2015, 2018, 2019; Harvey et al. 2016b), with studies highlighting that in vitro culture conditions used for ESC derivation and maintenance, as well as handling practices, can negatively affect their stability and ability to respond to stimuli, a significant challenge given that they must appropriately respond to environmental cues to give rise to all cell types within the body. Importantly, cellular changes have only been detected using metabolic analysis, in the absence of overt changes in pluripotency, emphasising the need to assess cell physiology as a marker of cell health, and the sensitivity of early stages of development to their surrounding environment. This is further exemplified in induced pluripotent stem cells (iPSCs), adult cells that have been reprogrammed to ESC-like cells. iPSCs exhibit deficits in metabolic reprogramming, resulting in the retention of somatic metabolic memory (Harvey et al. 2018), the degree of which can be modulated, in part, by oxygen availability during the reprogramming process, with standard atmospheric oxygen conditions negatively affecting resultant metabolism, genomic stability and the epigenetic landscape (Spyrou et al. 2019).
The use of atmospheric oxygen remains the norm not only for stem cells, but also embryo culture. However, these data suggest that such an approach may contribute to long-term changes in cell physiology and health, particularly given the dynamic links between nutrient availability, metabolism and the epigenetic landscape (Moussaieff et al. 2015; Harvey et al. 2016a, 2016b). This novel approach has the potential to change everything we thought we knew about cell biology and shed new light on ICM regulation and differentiation. This is especially important for ensuring embryo quality of IVF embryos before transfer and the subsequent health of resultant offspring, in line with the developmental origins of adult health and disease hypothesis.
SRB–Australian and New Zealand Placental Research Association (ANZPRA) Symposium
Speakers: Amanda Sferruzzi-Perri, William Rawlinson, Jo James, Fiona Brownfoot
This session explored novel diagnostics for a range pregnancy complications. In particular, the function of the placenta as the interface between mother and fetus has been a central focus of this area of research. The placenta plays major vital functions during pregnancy. Two major functions are: (1) transporting nutrients and oxygen from the mother to the fetus to allow healthy development of the growing fetus; and (2) producing hormones to maintain pregnancy and modulate the energy balance of the mother to aid fetal resource supply. In fact, altered resource allocation during pregnancy can lead to pregnancy complications affecting both mother and baby, including abnormal fetal growth and gestational diabetes. Insulin-like growth factor (IGF) 2 signalling via the phosphatidylinositol 3-kinase (PI3K) pathway is a key driver of fetal growth via the actions of IGF2 on the placenta under physiological and adverse pregnancy environments (for a review, see Sferruzzi-Perri et al. 2017). In response to environmental challenge, hypoxia and undernutrition interact via this pathway to control placental phenotype (Higgins et al. 2016). Genetic mouse models have enabled distinctions between maternal and fetal signals operating via IGF2/PI3K signalling that are responsible for adapting placental resource allocation (Sferruzzi-Perri et al. 2016). Recent evidence indicates that there is a threshold at which the mother and placenta may not be able to adapt to optimise fetal resource allocation and growth, although this depends on the specific gestational environment (Sferruzzi-Perri et al. 2019). Finally, via the production of hormones that are downstream of IGF2, the placenta may signal to the mother to alter her allocation of resources and control fetal growth.
The placenta also facilitates the transport of bacteria and viruses to the developing fetus. Congenital cytomegalovirus (CMV) is the most common, yet under-recognised, infectious cause of neonatal malformations in developed countries, in severe cases causing pre-eclampsia and fetal and neonatal death (Kenneson and Cannon 2007). A lack of uniform guidelines has impaired efforts to decrease the effects of CMV globally. Consequently, a recommendations group was convened in 2015 to establish guidelines for prevention and diagnosis (for a review, see Rawlinson et al. 2017). Ethical and practical barriers studying fetal infection have led to a lack of vaccine or pharmaceutical treatments, highlighting the ongoing need to understand the viral pathogenesis. Congenital CMV results from direct fetal infection, as well as indirect effects through placental infection (Hamilton et al. 2012). Ex vivo primary term and first trimester placental explant studies implicate altered dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) and Wnt signalling as central to CMV infection-mediated placental dysfunction. Specifically, CMV infection decreased trophoblast migration via elevated expression of Wnt-binding Receptor Tyrosine Kinase Like Orphan Receptor 2 (ROR2) (Huynh et al. 2019). Meanwhile, CMV replication within the placenta is dependent on DYRK signalling (Hamilton et al. 2018). Now, inhibitor studies are required to determine whether either or both targets could pave the way for the generation of the first therapeutic intervention. Early studies in vitro suggest such inhibitors reduce CMV replication and movement, paving the way for a new way of preventing placental and fetal damage (Hutterer et al. 2016; Hahn et al. 2018).
During pregnancy the placenta modifies the uterine vasculature to facilitate a 15-fold increase in maternal blood delivery to the placenta. Poor adaptation of the uterine circulation leads to decreased fetal nutrient and oxygen delivery, and consequently fetal growth restriction (FGR). However, the dynamic structural changes that occur in the uterine circulation during pregnancy and their functional consequences are poorly understood. Pathological pregnancies are detected by the presence of a uterine artery Doppler notch, which is generally attributed to inadequate spiral artery remodelling implicated in the pathogenesis of FGR. However, the contributions of the larger vessels in the uterine circulation that also undergo significant trophoblast-independent remodelling during pregnancy have largely been overlooked. A new collaboration encompassing physiological and bioengineering research has led to the development of virtual models of uteroplacental blood flow during pregnancy (Clark et al. 2018). These in silico models incorporate the arteriovenous anastomoses (AVA) in the maternal–fetal circulation for the first time and, in so doing, highlight a novel and potentially important role for the radial arteries in regulating volumetric blood delivery to the placenta (Clark et al. 2018; James et al. 2018). Indeed, models of the uterine artery Doppler waveform demonstrate that the radial arteries, rather than the spiral arteries, are the dominant contributors to the uterine artery Doppler notch frequently used to detect FGR pregnancies (Clark et al. 2018). These data also highlight an underappreciated role of the trophoblast plugs in the remodelling of the uterine vasculature (James et al. 2018; Saghian et al. 2019). Spiral and radial artery remodelling could be haemodynamically linked and should be considered as a complete and dynamic system in the diagnosis of FGR and to reduce the risk of stillbirths.
Maternal reporting of fetal movement is currently used a determinant of possible stillbirth, but with little efficacy. The partnering of clinical expertise with electrical engineers has led to the design of an electric sensing device that continuously monitors fetal heartbeat (electrocardiogram (ECG)). So far, a small pilot study (n = 10 pregnant women) (F. Brownfoot, unpubl. data) has developed predictive algorithm to remove noises coming from the maternal heartbeat and other interference from the fetal ECG. Now, a larger cohort of pregnant women will test a wearable patch allowing continuous monitoring of the fetal ECG from home (F. Brownfoot, unpubl. data). The day of birth is currently the most dangerous day in a lifetime associated with a high risk of mortality (Walker et al. 2014). Surprisingly, current available techniques to monitor fetal distress during labour are untimely and wrong 50% of the time. Therefore, there is a great need to develop new technologies to detect fetal distress in labour. Fiona Brownfoot, together with physicists and chemical engineers, has developed a device that measures a direct marker of fetal distress (F. Brownfoot, unpubl. data). This sensor will soon be tested in a preclinical fetal sheep model of hypoxia. Understanding the links between placental dysfunction and pregnancy complications continues to help unravel the pathophysiology of these disorders, which is a key prerequisite to developing improved diagnostics and therapeutics.
Big data in reproduction
Speakers: Claire Roberts, Katie Ayers, Grant Montgomery
Many researchers across the world of reproductive biology are now dealing with enormous datasets to further understand the complex regulation of various aspects of male and female fertility. The utility of such data, analysed together with new datasets, will likely pave the way for elucidating the causes of infertility states in both sexes, as well as pregnancy complications. There is also a need for the stringent analysis and mining of these data, with promising results seen as discussed below.
It is now well established that early life events shape lifelong health and that the placenta plays an integral role by regulating fetal health (for reviews, see Tarrade et al. 2015; Burton et al. 2016). One in four women experiences a pregnancy complication during their first pregnancy, which emphasises the need for further research into this area to understand the underlying causes. As part of a National Institutes of Health (NIH) Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Human Placenta Project study (unpubl. data), Claire Roberts and her team have collected a multitude of placental tissue and blood samples across all three trimesters of pregnancy from both normal and complicated (e.g. gestational diabetes, pre-eclampsia, preterm birth and intrauterine growth restriction) pregnancies. They have implemented a multiomics approach to survey the DNA, RNA and protein extracted from these samples, which is allowing them to investigate gene expression during normal development and any abnormalities in gene expression onset with pathologies of pregnancy. The mining of such data for biomarkers of healthy or aberrant pregnancies will be a major step forward in understanding the causes of these pathologies during pregnancy, as well as identifying the major changes occurring during the three trimesters in normal pregnancies. Interestingly, they report that the placenta is a comparatively highly hypothmethylated organ (Chatterjee et al. 2016), with increases in methylation gradually to term. However, in conditions such as pre-eclampsia, precocious methylation occurs, and this may contribute to the causative mechanisms of this disease (C. Roberts, unpubl. data). Using RNA sequencing, Roberts and her colleagues have also identified a temporal expression of genes regulating the immune response, as well as sex-specific differences in miRNA expression (C. Roberts, unpubl. data). The data generated from this RNA sequencing study and associated projects will be of major clinical benefit for states of pregnancy complication.
Disorders of sex development (DSD) represent a large spectrum of anatomical, gonadal or chromosomal sex abnormalities that affect both men and women (Ohnesorg et al. 2014; Croft et al. 2016). These disorders encompass common conditions such as hypospadias, where men have ectopic urethral openings (0.4–0.8% of men; Bouty et al. 2015) and are often diagnosed during childhood, meaning children suffer serious psychological and reproductive consequences, as well as rare conditions like 46,XX testicular DSD (sex reversal). Although DSD are largely genetic in nature, their cause remains unexplained in at least 50% of cases (Délot et al. 2017), with less than 13% of patients actually receiving a genetic diagnosis as part of their clinical care. To address this issue, Ayers and her colleagues have used a massive parallel sequencing approach in a cohort of 327 patients to target more than 1000 candidate genes believed to be required for normal sex development. This approach led to a highly successful genetic diagnostic rate in 43% of DSD patients, with 93 novel genetic variants reported across 28 genes (K. Ayers et al., unpubl. data). This raised the diagnostic rates threefold and, due to this success, this novel gene panel has been integrated into the standard screening pipeline within the Victorian Clinical Genetics Laboratories in Melbourne (Australia) and is now available to all patients nationally and internationally. Furthermore, to identify a genetic cause for the remaining idiopathic cases, Ayers and colleagues are now implementing whole-exome sequencing to probe for additional genetic variants across all protein-coding genes. Novel genetic variants identified with this more inclusive approach are currently being tested for their ability to cause DSD and affect sex development using various functional genomics models, including the fruit fly Drosophila (K. Ayers et al., unpubl. data).
Although increased use of next-generation sequencing techniques has improved our understanding of the complex genetic causes of certain disease states of male and female infertility (Maxwell et al. 2016; Oud et al. 2017), there is a subtle nature to many genetic risk factors that may be overlooked. Furthermore, there is likely a complex relationship between multiple genetic variants and/or epigenetic regulation that is causative for many infertility phenotypes. To further investigate, Grant Montgomery and his team have been undertaking GWAS in women with endometriosis (Fung et al. 2015). Many ‘hits’ identified within the GWAS have been localised to the non-coding regions of the genome, identifying a complex regulation of gene expression that is associated with the onset of this condition. The development of GWAS catalogues for disease types will likely create excellent sources for associations of certain genetic variants with particular diseases. However, the need for stringent testing of these associations will be required, including an assessment of multiple testing to minimise false-positive results. Another key area to address for the success of these approaches will be the specialised training of staff to understand bioinformatics and advanced statistics.
Conclusion
The SRB annual conference has long provided a platform for the dissemination of important contributions by SRB members in the field of reproductive science. The 2019 meeting has highlighted how these contributions are being translated to improve human health, agriculture and the conservation of species, with a focus on environmental effects on reproduction, the use and potential effects of big data in this field and key insights from researchers focusing on gamete biology, placental biology and embryogenesis. Importantly, several presentations showcased the transition from basic research to innovation and new technology, and how these technologies are being used to improve animal breeding efficiency, particularly in the horse, as well as for assisted reproduction in humans and for the protection of fertility during cancer treatment. The inclusion of the Endometriosis Workshop held immediately before the SRB meeting provided a critical update on how this key issue is being tackled at both a political and scientific level. This satellite meeting also served to unite scientists, clinicians and patient advocates from across Australia and New Zealand. Ultimately, tackling issues of reproduction from both a legislative and scientific angle will enable us to more rapidly turn discoveries into novel healthcare procedures and alleviate the financial and health burden of reproductive diseases such as endometriosis.
Conflict of interest
The authors declare no conflicts of interest.
Acknowledgements
The authors acknowledge the following speakers who presented their research in the symposia and thank them for their edits to the manuscript: Zamira Gibb (University of Newcastle), Jessica Dunleavy (Monash University), Peter Koopman (University of Queensland), Amanda Sferruzzi-Perri (University of Cambridge, UK), William Rawlinson (University of New South Wales), Jo James (University of Auckland), Fiona Brownfoot (The University of Melbourne), Claire Roberts (University of Adelaide), Katie Ayers (Murdoch Children’s Research Institute), Grant Montgomery (University of Queensland), Eva Dimitriadis (The University of Melbourne), Alexandra Harvey (The University of Melbourne), Nicole McPherson (Robinson Research Institute), Andrew Pask (The University of Melbourne), Bob Wong (Monash University), Peter Rogers (The University of Melbourne), Gita Mishra (University of Queensland), Linda Giudice (University of California, San Francisco), Melissa Parker (Centenary Hospital for Women and Children), Susan Evans (The Pelvic Pain Foundation of Australia), Stuart Brierley (South Australian Health and Medical Research Institute), Sally Mortlock (University of Queensland), Sarah Holdsworth-Carson (The University of Melbourne) and Caitlin Filby (Hudson Institute of Medical Research). The authors also acknowledge SRB President Moira O’Bryan and the Editor-in-Chief of Reproduction, Fertility and Development, Graeme Martin, for their support of the SRB Early Career Researchers and this review. This review of research conducted by members of the SRB did not receive any specific funding.
References
AbdelHafez, F. F., Desai, N., Abou-Setta, A. M., Falcone, T., and Goldfarb, J. (2010). Slow freezing, vitrification and ultra-rapid freezing of human embryos: a systematic review and meta-analysis. Reprod. Biomed. Online 20, 209–222.| Slow freezing, vitrification and ultra-rapid freezing of human embryos: a systematic review and meta-analysis.Crossref | GoogleScholarGoogle Scholar | 20113959PubMed |
Alshahrani, S., Ahmed, A. F., Gabr, A. H., Abalhassan, M., and Ahmad, G. (2016). The impact of body mass index on semen parameters in infertile men. Andrologia 48, 1125–1129.
| The impact of body mass index on semen parameters in infertile men.Crossref | GoogleScholarGoogle Scholar | 26847036PubMed |
Anglesio, M. S., and Yong, P. J. (2017). Endometriosis-associated ovarian cancers. Clin. Obstet. Gynecol. 60, 711–727.
| Endometriosis-associated ovarian cancers.Crossref | GoogleScholarGoogle Scholar | 28990985PubMed |
Anglesio, M. S., Bashashati, A., Wang, Y. K., Senz, J., Ha, G., Yang, W., Aniba, M. R., Prentice, L. M., Farahani, H., Li Chang, H., Karnezis, A. N., Marra, M. A., Yong, P. J., Hirst, M., Gilks, B., Shah, S. P., and Huntsman, D. G. (2015). Multifocal endometriotic lesions associated with cancer are clonal and carry a high mutation burden. J. Pathol. 236, 201–209.
| Multifocal endometriotic lesions associated with cancer are clonal and carry a high mutation burden.Crossref | GoogleScholarGoogle Scholar | 25692284PubMed |
Armour, M., Lawson, K., Wood, A., Smith, C. A., and Abbott, J. (2019). The cost of illness and economic burden of endometriosis and chronic pelvic pain in Australia: a national online survey. PLoS One 14, e0223316.
| The cost of illness and economic burden of endometriosis and chronic pelvic pain in Australia: a national online survey.Crossref | GoogleScholarGoogle Scholar | 31600241PubMed |
As-Sanie, S., Black, R., Giudice, L. C., Gray Valbrun, T., Gupta, J., Jones, B., Laufer, M. R., Milspaw, A. T., Missmer, S. A., Norman, A., Taylor, R. N., Wallace, K., Williams, Z., Yong, P. J., and Nebel, R. A. (2019). Assessing research gaps and unmet needs in endometriosis. Am. J. Obstet. Gynecol. 221, 86–94.
| Assessing research gaps and unmet needs in endometriosis.Crossref | GoogleScholarGoogle Scholar | 30790565PubMed |
Bhargava, A., Pathak, N., Sharma, R. S., Lohiya, N. K., and Mishra, P. K. (2017). Environmental impact on reproductive health: can biomarkers offer any help? J. Reprod. Infertil. 18, 336–340.
| 29062799PubMed |
Boretto, M., Cox, B., Noben, M., Hendriks, N., Fassbender, A., Roose, H., Amant, F., Timmerman, D., Tomassetti, C., Vanhie, A., Meuleman, C., Ferrante, M., and Vankelecom, H. (2017). Development of organoids from mouse and human endometrium showing endometrial epithelium physiology and long-term expandability. Development 144, 1775–1786.
| Development of organoids from mouse and human endometrium showing endometrial epithelium physiology and long-term expandability.Crossref | GoogleScholarGoogle Scholar | 28442471PubMed |
Boretto, M., Maenhoudt, N., Luo, X., Hennes, A., Boeckx, B., Bui, B., Heremans, R., Perneel, L., Kobayashi, H., Van Zundert, I., Brems, H., Cox, B., Ferrante, M., Uji, I. H., Koh, K. P., D’Hooghe, T., Vanhie, A., Vergote, I., Meuleman, C., Tomassetti, C., Lambrechts, D., Vriens, J., Timmerman, D., and Vankelecom, H. (2019). Patient-derived organoids from endometrial disease capture clinical heterogeneity and are amenable to drug screening. Nat. Cell Biol. 21, 1041–1051.
| Patient-derived organoids from endometrial disease capture clinical heterogeneity and are amenable to drug screening.Crossref | GoogleScholarGoogle Scholar | 31371824PubMed |
Bouty, A., Ayers, K. L., Pask, A., Heloury, Y., and Sinclair, A. H. (2015). The genetic and environmental factors underlying hypospadias. Sex Dev. 9, 239–259.
| The genetic and environmental factors underlying hypospadias.Crossref | GoogleScholarGoogle Scholar | 26613581PubMed |
Burton, G. J., Fowden, A. L., and Thornburg, K. L. (2016). Placental origins of chronic disease. Physiol. Rev. 96, 1509–1565.
| Placental origins of chronic disease.Crossref | GoogleScholarGoogle Scholar | 27604528PubMed |
Chatterjee, A., Macaulay, E. C., Rodger, E. J., Stockwell, P. A., Parry, M. F., Roberts, H. E., Slatter, T. L., Hung, N. A., Devenish, C. J., and Morison, I. M. (2016). Placental hypomethylation is more pronounced in genomic loci devoid of retroelements. G3 (Bethesda) 6, 1911–1921.
| Placental hypomethylation is more pronounced in genomic loci devoid of retroelements.Crossref | GoogleScholarGoogle Scholar | 27172225PubMed |
Chung, S. H., Franceschi, S., and Lambert, P. F. (2010). Estrogen and ERalpha: culprits in cervical cancer? Trends Endocrinol. Metab. 21, 504–511.
| Estrogen and ERalpha: culprits in cervical cancer?Crossref | GoogleScholarGoogle Scholar | 20456973PubMed |
Clark, A. R., James, J. L., Stevenson, G. N., and Collins, S. L. (2018). Understanding abnormal uterine artery Doppler waveforms: a novel computational model to explore potential causes within the utero-placental vasculature. Placenta 66, 74–81.
| Understanding abnormal uterine artery Doppler waveforms: a novel computational model to explore potential causes within the utero-placental vasculature.Crossref | GoogleScholarGoogle Scholar | 29884305PubMed |
Coughlan, C., Ledger, W., Wang, Q., Liu, F., Demirol, A., Gurgan, T., Cutting, R., Ong, K., Sallam, H., and Li, T. C. (2014). Recurrent implantation failure: definition and management. Reprod. Biomed. Online 28, 14–38.
| Recurrent implantation failure: definition and management.Crossref | GoogleScholarGoogle Scholar | 24269084PubMed |
Cousins, F. L., Msc, D. F. O, and Gargett, C. E. (2018). Endometrial stem/progenitor cells and their role in the pathogenesis of endometriosis. Best Pract. Res. Clin. Obstet. Gynaecol. 50, 27–38.
| Endometrial stem/progenitor cells and their role in the pathogenesis of endometriosis.Crossref | GoogleScholarGoogle Scholar | 29503126PubMed |
Cripps, S. M., Mattiske, D. M., Black, J. R., Risbridger, G. P., Govers, L. C., Phillips, T. R., and Pask, A. J. (2019). A loss of estrogen signaling in the aromatase deficient mouse penis results in mild hypospadias. Differentiation 109, 42–52.
| A loss of estrogen signaling in the aromatase deficient mouse penis results in mild hypospadias.Crossref | GoogleScholarGoogle Scholar | 31520742PubMed |
Croft, B., Ayers, K., Sinclair, A., and Ohnesorg, T. (2016). Review disorders of sex development: the evolving role of genomics in diagnosis and gene discovery. Birth Defects Res. C Embryo Today 108, 337–350.
| 28033663PubMed |
Cuman, C., Van Sinderen, M., Gantier, M. P., Rainczuk, K., Sorby, K., Rombauts, L., Osianlis, T., and Dimitriadis, E. (2015). Human blastocyst secreted microRNA regulate endometrial epithelial cell adhesion. EBioMedicine 2, 1528–1535.
| Human blastocyst secreted microRNA regulate endometrial epithelial cell adhesion.Crossref | GoogleScholarGoogle Scholar | 26629549PubMed |
Délot, E. C., Papp, J. C., The DSD-TRN Genetics Workgroup Sandberg, D. E., and Vilain, E. (2017). Genetics of disorders of sex development: the DSD-TRN experience. Endocrinol. Metab. Clin. North Am. 46, 519–537.
| Genetics of disorders of sex development: the DSD-TRN experience.Crossref | GoogleScholarGoogle Scholar | 28476235PubMed |
Dior, U. P., Kogan, L., Chill, H. H., Eizenberg, N., Simon, A., and Revel, A. (2014). Emerging roles of microRNA in the embryo–endometrium cross talk. Semin. Reprod. Med. 32, 402–409.
| Emerging roles of microRNA in the embryo–endometrium cross talk.Crossref | GoogleScholarGoogle Scholar | 24959822PubMed |
Evans, S. F., Brooks, T. A., Esterman, A. J., Hull, M. L., and Rolan, P. E. (2018). The comorbidities of dysmenorrhea: a clinical survey comparing symptom profile in women with and without endometriosis. J. Pain Res. 11, 3181–3194.
| The comorbidities of dysmenorrhea: a clinical survey comparing symptom profile in women with and without endometriosis.Crossref | GoogleScholarGoogle Scholar | 30588070PubMed |
Folmes, C. D., Nelson, T. J., Dzeja, P. P., and Terzic, A. (2012). Energy metabolism plasticity enables stemness programs. Ann. N. Y. Acad. Sci. 1254, 82–89.
| Energy metabolism plasticity enables stemness programs.Crossref | GoogleScholarGoogle Scholar | 22548573PubMed |
Ford, H. B., and Schust, D. J. (2009). Recurrent pregnancy loss: etiology, diagnosis, and therapy. Rev. Obstet. Gynecol. 2, 76–83.
| 19609401PubMed |
Fung, J. N., and Montgomery, G. W. (2018). Genetics of endometriosis: state of the art on genetic risk factors for endometriosis. Best Pract. Res. Clin. Obstet. Gynaecol. 50, 61–71.
| Genetics of endometriosis: state of the art on genetic risk factors for endometriosis.Crossref | GoogleScholarGoogle Scholar | 29506960PubMed |
Fung, J. N., Rogers, P. A., and Montgomery, G. W. (2015). Identifying the biological basis of GWAS hits for endometriosis. Biol. Reprod. 92, 87.
| Identifying the biological basis of GWAS hits for endometriosis.Crossref | GoogleScholarGoogle Scholar | 25695719PubMed |
Gardner, D. K., and Schoolcraft, W. B. (1999). In vitro culture of human blastocysts. In ‘Towards Reproductive Certainty: Fertility and Genetics Beyond 1999’, (Eds R. Jansen and D. Mortimer.) pp. 378–388. (CRC Press: Boca Raton)
Gardner, D. K. (2016). The impact of physiological oxygen during culture, and vitrification for cryopreservation, on the outcome of extended culture in human IVF. Reprod. Biomed. Online 32, 137–141.
| The impact of physiological oxygen during culture, and vitrification for cryopreservation, on the outcome of extended culture in human IVF.Crossref | GoogleScholarGoogle Scholar | 26687905PubMed |
Gardner, D. K., and Harvey, A. J. (2015). Blastocyst metabolism. Reprod. Fertil. Dev. 27, 638–654.
| Blastocyst metabolism.Crossref | GoogleScholarGoogle Scholar | 25751298PubMed |
Gardner, D. K., and Leese, H. J. (1987). Assessment of embryo viability prior to transfer by the noninvasive measurement of glucose uptake. J. Exp. Zool. 242, 103–105.
| Assessment of embryo viability prior to transfer by the noninvasive measurement of glucose uptake.Crossref | GoogleScholarGoogle Scholar | 3598508PubMed |
Gardner, D. K., and Wale, P. L. (2013). Analysis of metabolism to select viable human embryos for transfer. Fertil. Steril. 99, 1062–1072.
| Analysis of metabolism to select viable human embryos for transfer.Crossref | GoogleScholarGoogle Scholar | 23312219PubMed |
Gardner, D. K., Lane, M., and Schoolcraft, W. B. (2002). Physiology and culture of the human blastocyst. J. Reprod. Immunol. 55, 85–100.
| Physiology and culture of the human blastocyst.Crossref | GoogleScholarGoogle Scholar | 12062824PubMed |
Gardner, D. K., Wale, P. L., Collins, R., and Lane, M. (2011). Glucose consumption of single post-compaction human embryos is predictive of embryo sex and live birth outcome. Hum. Reprod. 26, 1981–1986.
| Glucose consumption of single post-compaction human embryos is predictive of embryo sex and live birth outcome.Crossref | GoogleScholarGoogle Scholar | 21572086PubMed |
Gargett, C. E., Schwab, K. E., Brosens, J. J., Puttemans, P., Benagiano, G., and Brosens, I. (2014). Potential role of endometrial stem/progenitor cells in the pathogenesis of early-onset endometriosis. Mol. Hum. Reprod. 20, 591–598.
| Potential role of endometrial stem/progenitor cells in the pathogenesis of early-onset endometriosis.Crossref | GoogleScholarGoogle Scholar | 24674992PubMed |
Ge, P., Ren, J., Harrington, A. M., Grundy, L., Castro, J., Brierley, S. M., and Hannig, G. (2019). Linaclotide treatment reduces endometriosis-associated vaginal hyperalgesia and mechanical allodynia through viscerovisceral cross-talk. Pain 160, 2566–2579.
| Linaclotide treatment reduces endometriosis-associated vaginal hyperalgesia and mechanical allodynia through viscerovisceral cross-talk.Crossref | GoogleScholarGoogle Scholar | 31335750PubMed |
Govers, L. C., Phillips, T. R., Mattiske, D. M., Rashoo, N., Black, J. R., Sinclair, A., Baskin, L. S., Risbridger, G. P., and Pask, A. J. (2019). A critical role for estrogen signaling in penis development. FASEB J. 33, 10383–10392.
| A critical role for estrogen signaling in penis development.Crossref | GoogleScholarGoogle Scholar | 31225966PubMed |
Grundy, L., Erickson, A., and Brierley, S. M. (2019). Visceral pain. Annu. Rev. Physiol. 81, 261–284.
| Visceral pain.Crossref | GoogleScholarGoogle Scholar | 30379615PubMed |
Gu, W., Gaeta, X., Sahakyan, A., Chan, A. B., Hong, C. S., Kim, R., Braas, D., Plath, K., Lowry, W. E., and Christofk, H. R. (2016). Glycolytic metabolism plays a functional role in regulating human pluripotent stem cell state. Cell Stem Cell 19, 476–490.
| Glycolytic metabolism plays a functional role in regulating human pluripotent stem cell state.Crossref | GoogleScholarGoogle Scholar | 27618217PubMed |
Ha, M., and Kim, V. N. (2014). Regulation of microRNA biogenesis. Nat. Rev. Mol. Cell Biol. 15, 509–524.
| Regulation of microRNA biogenesis.Crossref | GoogleScholarGoogle Scholar | 25027649PubMed |
Hahn, F., Hutterer, C., Henry, C., Hamilton, S. T., Strojan, H., Kraut, A., Schulte, U., Schutz, M., Kohrt, S., Wangen, C., Pfizer, J., Coute, Y., Rawlinson, W. D., Strobl, S., and Marschall, M. (2018). Novel cytomegalovirus-inhibitory compounds of the class pyrrolopyridines show a complex pattern of target binding that suggests an unusual mechanism of antiviral activity. Antiviral Res. 159, 84–94.
| Novel cytomegalovirus-inhibitory compounds of the class pyrrolopyridines show a complex pattern of target binding that suggests an unusual mechanism of antiviral activity.Crossref | GoogleScholarGoogle Scholar | 30268914PubMed |
Hamilton, S. T., Scott, G., Naing, Z., Iwasenko, J., Hall, B., Graf, N., Arbuckle, S., Craig, M. E., and Rawlinson, W. D. (2012). Human cytomegalovirus-induces cytokine changes in the placenta with implications for adverse pregnancy outcomes. PLoS One 7, e52899.
| Human cytomegalovirus-induces cytokine changes in the placenta with implications for adverse pregnancy outcomes.Crossref | GoogleScholarGoogle Scholar | 23300810PubMed |
Hamilton, S. T., Hutterer, C., Egilmezer, E., Steingruber, M., Milbradt, J., Marschall, M., and Rawlinson, W. D. (2018). Human cytomegalovirus utilises cellular dual-specificity tyrosine phosphorylation-regulated kinases during placental replication. Placenta 72–73, 10–19.
| Human cytomegalovirus utilises cellular dual-specificity tyrosine phosphorylation-regulated kinases during placental replication.Crossref | GoogleScholarGoogle Scholar | 30501876PubMed |
Harvey, A. J., Kind, K. L., Pantaleon, M., Armstrong, D. T., and Thompson, J. G. (2004). Oxygen-regulated gene expression in bovine blastocysts. Biol. Reprod. 71, 1108–1119.
| Oxygen-regulated gene expression in bovine blastocysts.Crossref | GoogleScholarGoogle Scholar | 15163614PubMed |
Harvey, A. J., Rathjen, J., and Gardner, D. K. (2016a). Metaboloepigenetic regulation of pluripotent stem cells. Stem Cells Int. 2016, 1816525.
| Metaboloepigenetic regulation of pluripotent stem cells.Crossref | GoogleScholarGoogle Scholar | 26839556PubMed |
Harvey, A. J., Rathjen, J., Yu, L. J., and Gardner, D. K. (2016b). Oxygen modulates human embryonic stem cell metabolism in the absence of changes in self-renewal. Reprod. Fertil. Dev. 28, 446–458.
| Oxygen modulates human embryonic stem cell metabolism in the absence of changes in self-renewal.Crossref | GoogleScholarGoogle Scholar | 25145274PubMed |
Harvey, A. J., O’Brien, C., Lambshead, J., Sheedy, J. R., Rathjen, J., Laslett, A. L., and Gardner, D. K. (2018). Physiological oxygen culture reveals retention of metabolic memory in human induced pluripotent stem cells. PLoS One 13, e0193949.
| Physiological oxygen culture reveals retention of metabolic memory in human induced pluripotent stem cells.Crossref | GoogleScholarGoogle Scholar | 29543848PubMed |
Higgins, J. S., Vaughan, O. R., Fernandez de Liger, E., Fowden, A. L., and Sferruzzi-Perri, A. N. (2016). Placental phenotype and resource allocation to fetal growth are modified by the timing and degree of hypoxia during mouse pregnancy. J. Physiol. 594, 1341–1356.
| Placental phenotype and resource allocation to fetal growth are modified by the timing and degree of hypoxia during mouse pregnancy.Crossref | GoogleScholarGoogle Scholar | 26377136PubMed |
Horne, A. W., Saunders, P. T. K., Abokhrais, I. M., Hogg, L., Group Endometriosis Priority Setting Partnership Steering (2017). Top ten endometriosis research priorities in the UK and Ireland. Lancet 389, 2191–2192.
| Top ten endometriosis research priorities in the UK and Ireland.Crossref | GoogleScholarGoogle Scholar | 28528751PubMed |
Hutterer, C., Hamilton, S., Steingruber, M., Zeittrager, I., Bahsi, H., Thuma, N., Naing, Z., Orfi, Z., Orfi, L., Socher, E., Sticht, H., Rawlinson, W., Chou, S., Haupt, V. J., and Marschall, M. (2016). The chemical class of quinazoline compounds provides a core structure for the design of anticytomegaloviral kinase inhibitors. Antiviral Res. 134, 130–143.
| The chemical class of quinazoline compounds provides a core structure for the design of anticytomegaloviral kinase inhibitors.Crossref | GoogleScholarGoogle Scholar | 27515131PubMed |
Huynh, K. T., van Zuylen, W. J., Ford, C. E., and Rawlinson, W. D. (2019). Selective modulation of Wnt-binding receptor tyrosine kinase ROR2 expression by human cytomegalovirus regulates trophoblast migration. J. Gen. Virol. 100, 99–104.
| Selective modulation of Wnt-binding receptor tyrosine kinase ROR2 expression by human cytomegalovirus regulates trophoblast migration.Crossref | GoogleScholarGoogle Scholar | 30431423PubMed |
James, J. L., Saghian, R., Perwick, R., and Clark, A. R. (2018). Trophoblast plugs: impact on utero-placental haemodynamics and spiral artery remodelling. Hum. Reprod. 33, 1430–1441.
| Trophoblast plugs: impact on utero-placental haemodynamics and spiral artery remodelling.Crossref | GoogleScholarGoogle Scholar | 29955830PubMed |
Jeng, H. A. (2014). Exposure to endocrine disrupting chemicals and male reproductive health. Front. Public Health 2, 55.
| Exposure to endocrine disrupting chemicals and male reproductive health.Crossref | GoogleScholarGoogle Scholar | 24926476PubMed |
Kenneson, A., and Cannon, M. J. (2007). Review and meta-analysis of the epidemiology of congenital cytomegalovirus (CMV) infection. Rev. Med. Virol. 17, 253–276.
| Review and meta-analysis of the epidemiology of congenital cytomegalovirus (CMV) infection.Crossref | GoogleScholarGoogle Scholar | 17579921PubMed |
Koot, Y. E. M., Teklenburg, G., Salker, M. S., Brosens, J. J., and Macklon, N. S. (2012). Molecular aspects of implantation failure. Biochim Biophys Acta. 1822, 1943–1950.
| Molecular aspects of implantation failure.Crossref | GoogleScholarGoogle Scholar |
Kropp, J., Salih, S. M., and Khatib, H. (2014). Expression of microRNAs in bovine and human pre-implantation embryo culture media. Front. Genet. 5, 91.
| Expression of microRNAs in bovine and human pre-implantation embryo culture media.Crossref | GoogleScholarGoogle Scholar | 24795753PubMed |
Lagesson, A., Saaristo, M., Brodin, T., Fick, J., Klaminder, J., Martin, J. M., and Wong, B. B. M. (2019). Fish on steroids: temperature-dependent effects of 17beta-trenbolone on predator escape, boldness, and exploratory behaviors. Environ. Pollut. 245, 243–252.
| Fish on steroids: temperature-dependent effects of 17beta-trenbolone on predator escape, boldness, and exploratory behaviors.Crossref | GoogleScholarGoogle Scholar | 30423539PubMed |
Lane, M., and Gardner, D. K. (1996). Selection of viable mouse blastocysts prior to transfer using a metabolic criterion. Hum. Reprod. 11, 1975–1978.
| Selection of viable mouse blastocysts prior to transfer using a metabolic criterion.Crossref | GoogleScholarGoogle Scholar | 8921074PubMed |
Lees, J. G., Rathjen, J., Sheedy, J. R., Gardner, D. K., and Harvey, A. J. (2015). Distinct profiles of human embryonic stem cell metabolism and mitochondria identified by oxygen. Reproduction 150, 367–382.
| Distinct profiles of human embryonic stem cell metabolism and mitochondria identified by oxygen.Crossref | GoogleScholarGoogle Scholar | 26159831PubMed |
Lees, J. G., Gardner, D. K., and Harvey, A. J. (2017). Pluripotent stem cell metabolism and mitochondria: beyond ATP. Stem Cells Int. 2017, 2874283.
| Pluripotent stem cell metabolism and mitochondria: beyond ATP.Crossref | GoogleScholarGoogle Scholar | 28804500PubMed |
Lees, J. G., Gardner, D. K., and Harvey, A. J. (2018). Mitochondrial and glycolytic remodeling during nascent neural differentiation of human pluripotent stem cells. Development 145, dev168997.
| Mitochondrial and glycolytic remodeling during nascent neural differentiation of human pluripotent stem cells.Crossref | GoogleScholarGoogle Scholar | 30266828PubMed |
Lees, J. G., Cliff, T. S., Gammilonghi, A., Ryall, J. G., Dalton, S., Gardner, D. K., and Harvey, A. J. (2019). Oxygen regulates human pluripotent stem cell metabolic flux. Stem Cells Int. 2019, 8195614.
| Oxygen regulates human pluripotent stem cell metabolic flux.Crossref | GoogleScholarGoogle Scholar | 31641358PubMed |
Manikkam, M., Tracey, R., Guerrero-Bosagna, C., and Skinner, M. K. (2012). Dioxin (TCDD) induces epigenetic transgenerational inheritance of adult onset disease and sperm epimutations. PLoS One 7, e46249.
| Dioxin (TCDD) induces epigenetic transgenerational inheritance of adult onset disease and sperm epimutations.Crossref | GoogleScholarGoogle Scholar | 23049995PubMed |
Maxwell, S. M., Colls, P., Hodes-Wertz, B., McCulloh, D. H., McCaffrey, C., Wells, D., Munne, S., and Grifo, J. A. (2016). Why do euploid embryos miscarry? A case-control study comparing the rate of aneuploidy within presumed euploid embryos that resulted in miscarriage or live birth using next-generation sequencing. Fertil. Steril. 106, 1414–1419e5.
| Why do euploid embryos miscarry? A case-control study comparing the rate of aneuploidy within presumed euploid embryos that resulted in miscarriage or live birth using next-generation sequencing.Crossref | GoogleScholarGoogle Scholar | 27692437PubMed |
McPherson, N. O., and Lane, M. (2015). Male obesity and subfertility, is it really about increased adiposity? Asian J. Androl. 17, 450–458.
| 25652636PubMed |
Meseguer, M., Herrero, J., Tejera, A., Hilligsoe, K. M., Ramsing, N. B., and Remohi, J. (2011). The use of morphokinetics as a predictor of embryo implantation. Hum. Reprod. 26, 2658–2671.
| The use of morphokinetics as a predictor of embryo implantation.Crossref | GoogleScholarGoogle Scholar | 21828117PubMed |
Morris, S. A., Grewal, S., Barrios, F., Patankar, S. N., Strauss, B., Buttery, L., Alexander, M., Shakesheff, K. M., and Zernicka-Goetz, M. (2012). Dynamics of anterior–posterior axis formation in the developing mouse embryo. Nat. Commun. 3, 673.
| Dynamics of anterior–posterior axis formation in the developing mouse embryo.Crossref | GoogleScholarGoogle Scholar | 22334076PubMed |
Mortlock, S., Restuadi, R., Levien, R., Girling, J. E., Holdsworth-Carson, S. J., Healey, M., Zhu, Z., Qi, T., Wu, Y., Lukowski, S. W., Rogers, P. A. W., Yang, J., McRae, A. F., Fung, J. N., and Montgomery, G. W. (2019). Genetic regulation of methylation in human endometrium and blood and gene targets for reproductive diseases. Clin. Epigenetics 11, 49.
| Genetic regulation of methylation in human endometrium and blood and gene targets for reproductive diseases.Crossref | GoogleScholarGoogle Scholar | 30871624PubMed |
Moussaieff, A., Kogan, N. M., and Aberdam, D. (2015). Concise review: energy metabolites: key mediators of the epigenetic state of pluripotency. Stem Cells 33, 2374–2380.
| Concise review: energy metabolites: key mediators of the epigenetic state of pluripotency.Crossref | GoogleScholarGoogle Scholar | 25873344PubMed |
Nguyen, H. P. T., Xiao, L., Deane, J. A., Tan, K. S., Cousins, F. L., Masuda, H., Sprung, C. N., Rosamilia, A., and Gargett, C. E. (2017). N-Cadherin identifies human endometrial epithelial progenitor cells by in vitro stem cell assays. Hum. Reprod. 32, 2254–2268.
| N-Cadherin identifies human endometrial epithelial progenitor cells by in vitro stem cell assays.Crossref | GoogleScholarGoogle Scholar |
Niakan, K. K., Han, J., Pedersen, R. A., Simon, C., and Pera, R. A. (2012). Human pre-implantation embryo development. Development 139, 829–841.
| Human pre-implantation embryo development.Crossref | GoogleScholarGoogle Scholar | 22318624PubMed |
Nilsson, E. E., Sadler-Riggleman, I., and Skinner, M. K. (2018). Environmentally induced epigenetic transgenerational inheritance of disease. Environ. Epigenet. 4, dvy016.
| Environmentally induced epigenetic transgenerational inheritance of disease.Crossref | GoogleScholarGoogle Scholar | 30038800PubMed |
Norwitz, E. R., Schust, D. J., and Fisher, S. J. (2001). Implantation and the survival of early pregnancy. N. Engl. J. Med. 345, 1400–1408.
| Implantation and the survival of early pregnancy.Crossref | GoogleScholarGoogle Scholar | 11794174PubMed |
Ohnesorg, T., Vilain, E., and Sinclair, A. H. (2014). The genetics of disorders of sex development in humans. Sex Dev. 8, 262–272.
| The genetics of disorders of sex development in humans.Crossref | GoogleScholarGoogle Scholar | 24504012PubMed |
Oud, M. S., Ramos, L., O’Bryan, M. K., McLachlan, R. I., Okutman, Ö., Viville, S., de Vries, P. F., Smeets, D. F. C. M., Lugtenberg, D., Hehir-Kwa, J. Y., Gilissen, C., van de Vorst, M., Vissers, L. E. L. M., Hoischen, A., Meijerink, A. M., Fleischer, K., Veltman, J. A., and Noordam, M. J. (2017). Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia. Hum. Mutat. 38, 1592–1605.
| Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia.Crossref | GoogleScholarGoogle Scholar | 28801929PubMed |
Palmer, N. O., Bakos, H. W., Owens, J. A., Setchell, B. P., and Lane, M. (2012). Diet and exercise in an obese mouse fed a high-fat diet improve metabolic health and reverse perturbed sperm function. Am. J. Physiol. Endocrinol. Metab. 302, E768–E780.
| Diet and exercise in an obese mouse fed a high-fat diet improve metabolic health and reverse perturbed sperm function.Crossref | GoogleScholarGoogle Scholar | 22252945PubMed |
Pauli, E. M., Legro, R. S., Demers, L. M., Kunselman, A. R., Dodson, W. C., and Lee, P. A. (2008). Diminished paternity and gonadal function with increasing obesity in men. Fertil. Steril. 90, 346–351.
| Diminished paternity and gonadal function with increasing obesity in men.Crossref | GoogleScholarGoogle Scholar | 18291378PubMed |
Paulozzi, L. J., Erickson, J. D., and Jackson, R. J. (1997). Hypospadias trends in two US surveillance systems. Pediatrics 100, 831–834.
| Hypospadias trends in two US surveillance systems.Crossref | GoogleScholarGoogle Scholar | 9346983PubMed |
Rawlinson, W. D., Boppana, S. B., Fowler, K. B., Kimberlin, D. W., Lazzarotto, T., Alain, S., Daly, K., Doutre, S., Gibson, L., Giles, M. L., Greenlee, J., Hamilton, S. T., Harrison, G. J., Hui, L., Jones, C. A., Palasanthiran, P., Schleiss, M. R., Shand, A. W., and van Zuylen, W. J. (2017). Congenital cytomegalovirus infection in pregnancy and the neonate: consensus recommendations for prevention, diagnosis, and therapy. Lancet Infect. Dis. 17, e177–e188.
| Congenital cytomegalovirus infection in pregnancy and the neonate: consensus recommendations for prevention, diagnosis, and therapy.Crossref | GoogleScholarGoogle Scholar | 28291720PubMed |
Rehman, S., Usman, Z., Rehman, S., AlDraihem, M., Rehman, N., Rehman, I., and Ahmad, G. (2018). Endocrine disrupting chemicals and impact on male reproductive health. Transl. Androl. Urol. 7, 490–503.
| Endocrine disrupting chemicals and impact on male reproductive health.Crossref | GoogleScholarGoogle Scholar | 30050807PubMed |
Revel, A., Achache, H., Stevens, J., Smith, Y., and Reich, R. (2011). MicroRNAs are associated with human embryo implantation defects. Hum. Reprod. 26, 2830–2840.
| MicroRNAs are associated with human embryo implantation defects.Crossref | GoogleScholarGoogle Scholar | 21849299PubMed |
Rier, S., and Foster, W. G. (2002). Environmental dioxins and endometriosis. Toxicol. Sci. 70, 161–170.
| Environmental dioxins and endometriosis.Crossref | GoogleScholarGoogle Scholar | 12441361PubMed |
Rogers, P. A., Adamson, G. D., Al-Jefout, M., Becker, C. M., D’Hooghe, T. M., Dunselman, G. A., Fazleabas, A., Giudice, L. C., Horne, A. W., Hull, M. L., Hummelshoj, L., Missmer, S. A., Montgomery, G. W., Stratton, P., Taylor, R. N., Rombauts, L., Saunders, P. T., Vincent, K., Zondervan, K. T., Wes Werf Consortium for Research Priorities in Endometriosis (2017). Research priorities for endometriosis. Reprod. Sci. 24, 202–226.
| Research priorities for endometriosis.Crossref | GoogleScholarGoogle Scholar | 27368878PubMed |
Rosenbluth, E. M., Shelton, D. N., Wells, L. M., Sparks, A. E., and Van Voorhis, B. J. (2014). Human embryos secrete microRNAs into culture media – a potential biomarker for implantation. Fertil. Steril. 101, 1493–1500.
| Human embryos secrete microRNAs into culture media – a potential biomarker for implantation.Crossref | GoogleScholarGoogle Scholar | 24786747PubMed |
Saghian, R., Bogle, G., James, J. L., and Clark, A. R. (2019). Establishment of maternal blood supply to the placenta: insights into plugging, unplugging and trophoblast behaviour from an agent-based model. Interface Focus 9, 20190019.
| Establishment of maternal blood supply to the placenta: insights into plugging, unplugging and trophoblast behaviour from an agent-based model.Crossref | GoogleScholarGoogle Scholar | 31485310PubMed |
Sferruzzi-Perri, A. N., Lopez-Tello, J., Fowden, A. L., and Constancia, M. (2016). Maternal and fetal genomes interplay through phosphoinositol 3-kinase(PI3K)–p110alpha signaling to modify placental resource allocation. Proc. Natl Acad. Sci. USA 113, 11255–11260.
| Maternal and fetal genomes interplay through phosphoinositol 3-kinase(PI3K)–p110alpha signaling to modify placental resource allocation.Crossref | GoogleScholarGoogle Scholar | 27621448PubMed |
Sferruzzi-Perri, A. N., Sandovici, I., Constancia, M., and Fowden, A. L. (2017). Placental phenotype and the insulin-like growth factors: resource allocation to fetal growth. J. Physiol. 595, 5057–5093.
| Placental phenotype and the insulin-like growth factors: resource allocation to fetal growth.Crossref | GoogleScholarGoogle Scholar | 28337745PubMed |
Sferruzzi-Perri, A. N., Higgins, J. S., Vaughan, O. R., Murray, A. J., and Fowden, A. L. (2019). Placental mitochondria adapt developmentally and in response to hypoxia to support fetal growth. Proc. Natl Acad. Sci. USA 116, 1621–1626.
| Placental mitochondria adapt developmentally and in response to hypoxia to support fetal growth.Crossref | GoogleScholarGoogle Scholar | 30655345PubMed |
Shayeb, A. G., Harrild, K., Mathers, E., and Bhattacharya, S. (2011). An exploration of the association between male body mass index and semen quality. Reprod. Biomed. Online 23, 717–723.
| An exploration of the association between male body mass index and semen quality.Crossref | GoogleScholarGoogle Scholar | 22019618PubMed |
Shyh-Chang, N., and Daley, G. Q. (2015). Metabolic switches linked to pluripotency and embryonic stem cell differentiation. Cell Metab. 21, 349–350.
| Metabolic switches linked to pluripotency and embryonic stem cell differentiation.Crossref | GoogleScholarGoogle Scholar | 25738450PubMed |
Simon, A., and Laufer, N. (2012). Assessment and treatment of repeated implantation failure (RIF). J. Assist. Reprod. Genet. 29, 1227–1239.
| Assessment and treatment of repeated implantation failure (RIF).Crossref | GoogleScholarGoogle Scholar | 22976427PubMed |
Simsa, P., Mihalyi, A., Schoeters, G., Koppen, G., Kyama, C. M., Den Hond, E. M., Fulop, V., and D’Hooghe, T. M. (2010). Increased exposure to dioxin-like compounds is associated with endometriosis in a case-control study in women. Reprod. Biomed. Online 20, 681–688.
| Increased exposure to dioxin-like compounds is associated with endometriosis in a case-control study in women.Crossref | GoogleScholarGoogle Scholar | 20211585PubMed |
Spyrou, J., Gardner, D. K., and Harvey, A. J. (2019). Metabolomic and transcriptional analyses reveal atmospheric oxygen during human induced pluripotent stem cell generation impairs metabolic reprogramming. Stem Cells 37, 1042–1056.
| Metabolomic and transcriptional analyses reveal atmospheric oxygen during human induced pluripotent stem cell generation impairs metabolic reprogramming.Crossref | GoogleScholarGoogle Scholar | 31042329PubMed |
Stewart, T. M., Liu, D. Y., Garrett, C., Jorgensen, N., Brown, E. H., and Baker, H. W. (2009). Associations between andrological measures, hormones and semen quality in fertile Australian men: inverse relationship between obesity and sperm output. Hum. Reprod. 24, 1561–1568.
| Associations between andrological measures, hormones and semen quality in fertile Australian men: inverse relationship between obesity and sperm output.Crossref | GoogleScholarGoogle Scholar | 19351657PubMed |
Suda, K., Nakaoka, H., Yoshihara, K., Ishiguro, T., Tamura, R., Mori, Y., Yamawaki, K., Adachi, S., Takahashi, T., Kase, H., Tanaka, K., Yamamoto, T., Motoyama, T., Inoue, I., and Enomoto, T. (2018). Clonal expansion and diversification of cancer-associated mutations in endometriosis and normal endometrium. Cell Rep. 24, 1777–1789.
| Clonal expansion and diversification of cancer-associated mutations in endometriosis and normal endometrium.Crossref | GoogleScholarGoogle Scholar | 30110635PubMed |
Takai, Y., and Nakanishi, H. (2003). Nectin and afadin: novel organizers of intercellular junctions. J. Cell Sci. 116, 17–27.
| Nectin and afadin: novel organizers of intercellular junctions.Crossref | GoogleScholarGoogle Scholar | 12456712PubMed |
Takai, Y., Irie, K., Shimizu, K., Sakisaka, T., and Ikeda, W. (2003). Nectins and nectin-like molecules: roles in cell adhesion, migration, and polarization. Cancer Sci. 94, 655–667.
| Nectins and nectin-like molecules: roles in cell adhesion, migration, and polarization.Crossref | GoogleScholarGoogle Scholar | 12901789PubMed |
Takai, Y., Miyoshi, J., Ikeda, W., and Ogita, H. (2008). Nectins and nectin-like molecules: roles in contact inhibition of cell movement and proliferation. Nat. Rev. Mol. Cell Biol. 9, 603.
| Nectins and nectin-like molecules: roles in contact inhibition of cell movement and proliferation.Crossref | GoogleScholarGoogle Scholar | 18648374PubMed |
Tan, B. K., Vandekerckhove, P., Kennedy, R., and Keay, S. D. (2005). Investigation and current management of recurrent IVF treatment failure in the UK. BJOG 112, 773–780.
| Investigation and current management of recurrent IVF treatment failure in the UK.Crossref | GoogleScholarGoogle Scholar | 15924536PubMed |
Tarrade, A., Panchenko, P., Junien, C., and Gabory, A. (2015). Placental contribution to nutritional programming of health and diseases: epigenetics and sexual dimorphism. J. Exp. Biol. 218, 50–58.
| Placental contribution to nutritional programming of health and diseases: epigenetics and sexual dimorphism.Crossref | GoogleScholarGoogle Scholar | 25568451PubMed |
Tomkins, P., Saaristo, M., Allinson, M., and Wong, B. B. M. (2016). Exposure to an agricultural contaminant, 17beta-trenbolone, impairs female mate choice in a freshwater fish. Aquat. Toxicol. 170, 365–370.
| Exposure to an agricultural contaminant, 17beta-trenbolone, impairs female mate choice in a freshwater fish.Crossref | GoogleScholarGoogle Scholar | 26466515PubMed |
Turco, M. Y., Gardner, L., Hughes, J., Cindrova-Davies, T., Gomez, M. J., Farrell, L., Hollinshead, M., Marsh, S. G. E., Brosens, J. J., Critchley, H. O., Simons, B. D., Hemberger, M., Koo, B. K., Moffett, A., and Burton, G. J. (2017). Long-term, hormone-responsive organoid cultures of human endometrium in a chemically defined medium. Nat. Cell Biol. 19, 568–577.
| Long-term, hormone-responsive organoid cultures of human endometrium in a chemically defined medium.Crossref | GoogleScholarGoogle Scholar | 28394884PubMed |
Valentijn, A. J., Palial, K., Al-Lamee, H., Tempest, N., Drury, J., Von Zglinicki, T., Saretzki, G., Murray, P., Gargett, C. E., and Hapangama, D. K. (2013). SSEA-1 isolates human endometrial basal glandular epithelial cells: phenotypic and functional characterization and implications in the pathogenesis of endometriosis. Hum. Reprod. 28, 2695–2708.
| SSEA-1 isolates human endometrial basal glandular epithelial cells: phenotypic and functional characterization and implications in the pathogenesis of endometriosis.Crossref | GoogleScholarGoogle Scholar | 23847113PubMed |
Walker, K. F., Cohen, A. L., Walker, S. H., Allen, K. M., Baines, D. L., and Thornton, J. G. (2014). The dangers of the day of birth. BJOG 121, 714–718.
| The dangers of the day of birth.Crossref | GoogleScholarGoogle Scholar | 24521517PubMed |
Winship, A., Ton, A., Van Sinderen, M., Menkhorst, E., Rainczuk, K., Griffiths, M., Cuman, C., and Dimitriadis, E. (2018). Mouse double minute homologue 2 (MDM2) downregulation by miR-661 impairs human endometrial epithelial cell adhesive capacity. Reprod. Fertil. Dev. 30, 477–486.
| Mouse double minute homologue 2 (MDM2) downregulation by miR-661 impairs human endometrial epithelial cell adhesive capacity.Crossref | GoogleScholarGoogle Scholar | 28847363PubMed |
Yang, B., Chen, R., Liang, X., Shi, J., Wu, X., Zhang, Z., and Chen, X. (2019). Estrogen enhances endometrial cancer cells proliferation by upregulation of prohibitin. J. Cancer 10, 1616–1621.
| Estrogen enhances endometrial cancer cells proliferation by upregulation of prohibitin.Crossref | GoogleScholarGoogle Scholar | 31205517PubMed |
Zhang, J., Khvorostov, I., Hong, J. S., Oktay, Y., Vergnes, L., Nuebel, E., Wahjudi, P. N., Setoguchi, K., Wang, G., Do, A., Jung, H. J., McCaffery, J. M., Kurland, I. J., Reue, K., Lee, W. N., Koehler, C. M., and Teitell, M. A. (2011). UCP2 regulates energy metabolism and differentiation potential of human pluripotent stem cells. EMBO J. 30, 4860–4873.
| UCP2 regulates energy metabolism and differentiation potential of human pluripotent stem cells.Crossref | GoogleScholarGoogle Scholar | 22085932PubMed |
Zhao, Y., Zacur, H., Cheadle, C., Ning, N., Fan, J., and Vlahos, N. F. (2012). Effect of luteal-phase support on endometrial microRNA expression following controlled ovarian stimulation. Reprod. Biol. Endocrinol. 10, 72.
| Effect of luteal-phase support on endometrial microRNA expression following controlled ovarian stimulation.Crossref | GoogleScholarGoogle Scholar | 22950660PubMed |
Zinaman, M. J., Clegg, E. D., Brown, C. C., O’Connor, J., and Selevan, S. G. (1996). Estimates of human fertility and pregnancy loss. Fertil. Steril. 65, 503–509.
| Estimates of human fertility and pregnancy loss.Crossref | GoogleScholarGoogle Scholar | 8774277PubMed |