Interleukin 11: similar or opposite roles in female reproduction and reproductive cancer?

References

Australian Institute of Health and Welfare (AIHW) (2012) ‘Gynaecological cancers in Australia: an overview. Cancer series no. 70. CAN 66’. (AIHW: Canberra.)

Ain, R., Trinh, M. L., and Soares, M. J. (2004). Interleukin-11 signaling is required for the differentiation of natural killer cells at the maternal–fetal interface. Dev. Dyn. 231, 700–708.
| Interleukin-11 signaling is required for the differentiation of natural killer cells at the maternal–fetal interface.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhtFakurzM&md5=366ec7227c4b3284d4fee36615823b25CAS | 15499555PubMed |

Amant, F., Moerman, P., Neven, P., Timmerman, D., Limbergen, E. V., and Vergote, I. (2005). Endometrial cancer. Lancet 366, 491–505.
| Endometrial cancer.Crossref | GoogleScholarGoogle Scholar | 16084259PubMed |

Bao, L., Devi, Y. S., Bowen-Shauver, J., Ferguson-Gottschall, S., Robb, L., and Gibori, G. (2006). The role of interleukin-11 in pregnancy involves up-regulation of alpha2-macroglobulin gene through janus kinase 2-signal transducer and activator of transcription 3 pathway in the decidua. Mol. Endocrinol. 20, 3240–3250.
| The role of interleukin-11 in pregnancy involves up-regulation of alpha2-macroglobulin gene through janus kinase 2-signal transducer and activator of transcription 3 pathway in the decidua.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtlWks77F&md5=cd97ca2ef04d7280c82087e70ac8a16fCAS | 16959875PubMed |

Basar, M., Yen, C., Buchwalder, L., Murk, W., Huang, S., Godlewski, K., Kocamaz, E., Arda, O., Schatz, F., Lockwood, C., and Kayisli, U. (2010). Preeclampsia-related increase of interleukin-11 expression in human decidual cells. Reproduction 140, 605–612.
| Preeclampsia-related increase of interleukin-11 expression in human decidual cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtlCqurvM&md5=456189746ce34164cb95b44a53f072a4CAS | 20668109PubMed |

Bellone, G., Smirne, C., Mauri, F. A., Tonel, E., Carbone, A., Buffolino, A., Dughera, L., Robecchi, A., Pirisi, M., and Emanuelli, G. (2006). Cytokine expression profile in human pancreatic carcinoma cells and in surgical specimens: implications for survival. Cancer Immunol. Immunother. 55, 684–698.
| Cytokine expression profile in human pancreatic carcinoma cells and in surgical specimens: implications for survival.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhvFWqt7w%3D&md5=4ad73a6245930883bcb19231b1cd1c82CAS | 16094523PubMed |

Benedet, J. L., Pecorelli, S., Bender, H., Benedet, J., and Ngan, H. (2000). Cancer of the corpus uteri. Int. J. Gynaecol. Obstet. 70, 207–208.
| 10960610PubMed |

Bilinski, P., Roopenian, D., and Gossler, A. (1998). Maternal IL-11Ralpha function is required for normal decidua and fetoplacental development in mice. Genes Dev. 12, 2234–2243.
| Maternal IL-11Ralpha function is required for normal decidua and fetoplacental development in mice.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXltVSht78%3D&md5=1f6f6a174d030caf87390f9c5345a1b3CAS | 9679067PubMed |

Bulmer, J. N., Morrison, L., and Johnson, P. M. (1988). Expression of the proliferation markers Ki67 and transferrin receptor by human trophoblast populations. J. Reprod. Immunol. 14, 291–302.
| Expression of the proliferation markers Ki67 and transferrin receptor by human trophoblast populations.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1MXpt1Omsw%3D%3D&md5=12cc55c8814e06c8772554c84d7b5b62CAS | 3225818PubMed |

Burton, G. J., Yung, H. W., Cindrova-Davies, T., and Charnock-Jones, D. S. (2009). Placental endoplasmic reticulum stress and oxidative stress in the pathophysiology of unexplained intrauterine growth restriction and early onset preeclampsia. Placenta 30, S43–S48.
| Placental endoplasmic reticulum stress and oxidative stress in the pathophysiology of unexplained intrauterine growth restriction and early onset preeclampsia.Crossref | GoogleScholarGoogle Scholar | 19081132PubMed |

Burton, G. J., Jauniaux, E., and Charnock-Jones, D. S. (2010). The influence of the intrauterine environment on human placental development. Int. J. Dev. Biol. 54, 303–312.
| The influence of the intrauterine environment on human placental development.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXltVajtb8%3D&md5=b20f3bf852930d796a4d54e60f3eb80aCAS | 19757391PubMed |

Campbell, C. L., Guardiani, R., Ollari, C., Nelson, B. E., Quesenberry, P. J., and Savarese, T. M. (2001a). Interleukin-11 receptor expression in primary ovarian carcinomas. Gynecol. Oncol. 80, 121–127.
| Interleukin-11 receptor expression in primary ovarian carcinomas.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXmsFCjtw%3D%3D&md5=a60eade40425ca167a6b59fbde3f83f9CAS | 11161848PubMed |

Campbell, C. L., Jiang, Z., Savarese, D. M., and Savarese, T. M. (2001b). Increased expression of the interleukin-11 receptor and evidence of STAT3 activation in prostate carcinoma. Am. J. Pathol. 158, 25–32.
| Increased expression of the interleukin-11 receptor and evidence of STAT3 activation in prostate carcinoma.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXmsFKrsw%3D%3D&md5=d3d36202c29a7dc07770feb40ad4e73cCAS | 11141475PubMed |

Castellucci, M., Theelen, T., Pompili, E., Fumagalli, L., De Renzis, G., and Muhlhauser, J. (1994). Immunohistochemical localization of serine-protease inhibitors in the human placenta. Cell Tissue Res. 278, 283–289.
| Immunohistochemical localization of serine-protease inhibitors in the human placenta.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXit1Wmtbg%3D&md5=a1fb9f19c4cd69ea81b4909ee14d8a05CAS | 7528097PubMed |

Chen, H., Lin, C., Chao, K., Wu, M., Yang, Y., and Ho, H. (2002). Defective production of interleukin-11 by decidua and chorionic villi in human anembryonic pregnancy. J. Clin. Endocrinol. Metab. 87, 2320–2328.
| 1:CAS:528:DC%2BD38XjsFGgsrw%3D&md5=005916e6aa2d984c821663956d0a2299CAS | 11994383PubMed |

Chen, C. L., Hsieh, F. C., Lieblein, J. C., Brown, J., Chan, C., Wallace, J. A., Cheng, G., Hall, B. M., and Lin, J. (2007). Stat3 activation in human endometrial and cervical cancers. Br. J. Cancer 96, 591–599.
| Stat3 activation in human endometrial and cervical cancers.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhvV2jtrc%3D&md5=0ef0981400141f56311c7efeb0671007CAS | 17311011PubMed |

Corvinus, F. M., Fitzgerald, J. S., Friedrich, K., and Markert, U. R. (2003). Evidence for a correlation between trophoblast invasiveness and STAT3 activity. Am. J. Reprod. Immunol. 50, 316–321.
| Evidence for a correlation between trophoblast invasiveness and STAT3 activity.Crossref | GoogleScholarGoogle Scholar | 14672334PubMed |

Davidson, A. J., Freeman, S. A., Crosier, K. E., Wood, C. R., and Crosier, P. S. (1997). Expression of murine interleukin 11 and its receptor alpha-chain in adult and embryonic tissues. Stem Cells 15, 119–124.
| Expression of murine interleukin 11 and its receptor alpha-chain in adult and embryonic tissues.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2sXis1GqtLc%3D&md5=2586c8c71074c075fde0f21b1ae42f2eCAS | 9090788PubMed |

Dessus-Babus, S., Darville, T. L., Cuozzo, F. P., Ferguson, K., and Wyrick, P. B. (2002). Differences in innate immune responses (in vitro) to HeLa cells infected with nondisseminating serovar E and disseminating serovar L2 of Chlamydia trachomatis. Infect. Immun. 70, 3234–3248.
| Differences in innate immune responses (in vitro) to HeLa cells infected with nondisseminating serovar E and disseminating serovar L2 of Chlamydia trachomatis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XktFGhsrs%3D&md5=06e0361a93a37893acc12918f74c64f8CAS | 12011019PubMed |

Di Cristofano, A., and Ellenson, L. H. (2007). Endometrial carcinoma. Annu. Rev. Pathol. 2, 57–85.
| Endometrial carcinoma.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXivV2isLY%3D&md5=9ed0e153f66f490db45fd1ddd09c5c02CAS | 18039093PubMed |

Dimitriadis, E., Salamonsen, L. A., and Robb, L. (2000). Expression of interleukin-11 during the human menstrual cycle: coincidence with stromal cell decidualization and relationship to leukaemia inhibitory factor and prolactin. Mol. Hum. Reprod. 6, 907–914.
| Expression of interleukin-11 during the human menstrual cycle: coincidence with stromal cell decidualization and relationship to leukaemia inhibitory factor and prolactin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXnslSgt7o%3D&md5=0041e85ee0bf880edde35f502eac1decCAS | 11006319PubMed |

Dimitriadis, E., Robb, L., and Salamonsen, L. (2002). Interleukin 11 advances progesterone-induced decidualization of human endometrial stromal cells. Mol. Hum. Reprod. 8, 636–643.
| Interleukin 11 advances progesterone-induced decidualization of human endometrial stromal cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XlvFKlsb4%3D&md5=1b918b91a5e24ca6ce7c669eddd99794CAS | 12087078PubMed |

Dimitriadis, E., Robb, L., Liu, Y., Enders, A., Martin, H., Stoikos, C., Wallace, E., and Salamonsen, L. A. (2003). IL-11 and IL-11Rα immunolocalisation at primate implantation sites supports a role for IL-11 in placentation and fetal development. Reprod. Biol. Endocrinol. 1, 34–44.
| IL-11 and IL-11Rα immunolocalisation at primate implantation sites supports a role for IL-11 in placentation and fetal development.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2cznslylsw%3D%3D&md5=82ac24e809ace71fe58afaaa02dedf3fCAS | 12740032PubMed |

Dimitriadis, E., White, C. A., Jones, R. L., and Salamonsen, L. A. (2005). Cytokines, chemokines and growth factors in endometrium related to implantation. Hum. Reprod. Update 11, 613–630.
| Cytokines, chemokines and growth factors in endometrium related to implantation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtFWltrzJ&md5=8123787f713e53567c9c9092894490c0CAS | 16006437PubMed |

Dimitriadis, E., Stoikos, C., Stafford-Bell, M., Clark, I., Paiva, P., Kovacs, G., and Salamonsen, L. A. (2006a). Interleukin-11, IL-11 receptoralpha and leukemia inhibitory factor are dysregulated in endometrium of infertile women with endometriosis during the implantation window. J. Reprod. Immunol. 69, 53–64.
| Interleukin-11, IL-11 receptoralpha and leukemia inhibitory factor are dysregulated in endometrium of infertile women with endometriosis during the implantation window.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XnslyktQ%3D%3D&md5=c1fbdfbe7c7bfe3b88fe11333566ef2fCAS | 16310857PubMed |

Dimitriadis, E., Stoikos, C., Tan, Y. L., and Salamonsen, L. A. (2006b). Interleukin 11 signaling components signal transducer and activator of transcription 3 (STAT3) and suppressor of cytokine signaling 3 (SOCS3) regulate human endometrial stromal cell differentiation. Endocrinology 147, 3809–3817.
| Interleukin 11 signaling components signal transducer and activator of transcription 3 (STAT3) and suppressor of cytokine signaling 3 (SOCS3) regulate human endometrial stromal cell differentiation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XnsVWmsrc%3D&md5=6e76fde2898346134ec44f38aa46ac1aCAS | 16709613PubMed |

Dimitriadis, E., Sharkey, A., Tan, Y., Salamonsen, L. A., and Sherwin, J. (2007). Immunolocalisation of phosphorylated STAT3, interleukin 11 and leukaemia inhibitory factor in endometrium of women with unexplained infertility during the implantation window. Reprod. Biol. Endocrinol. 5, 44–51.
| Immunolocalisation of phosphorylated STAT3, interleukin 11 and leukaemia inhibitory factor in endometrium of women with unexplained infertility during the implantation window.Crossref | GoogleScholarGoogle Scholar | 18047677PubMed |

Du, X. X., and Williams, D. A. (1994). Interleukin-11: a multifunctional growth factor derived from the hematopoietic microenvironment. Blood 83, 2023–2030.
| 1:CAS:528:DyaK2cXis1Omu7c%3D&md5=5e0e69a8de531d77194e1f55c348babeCAS | 7512836PubMed |

Elias, J. A., Zheng, T., Einarsson, O., Landry, M., Trow, T., Rebert, N., and Panuska, J. (1994). Epithelial interleukin-11. Regulation by cytokines, respiratory syncytial virus, and retinoic acid. J. Biol. Chem. 269, 22 261–22 268.
| 1:CAS:528:DyaK2cXlslOnsr4%3D&md5=b9f3802dd7f54900da25adcaf0cdcd59CAS |

Ellis, M., Hedstrom, U., Frampton, C., Alizadeh, H., Kristensen, J., Shammas, F. V., and al-Ramadi, B. K. (2006). Modulation of the systemic inflammatory response by recombinant human interleukin-11: a prospective randomized placebo controlled clinical study in patients with hematological malignancy. Clin. Immunol. 120, 129–137.
| Modulation of the systemic inflammatory response by recombinant human interleukin-11: a prospective randomized placebo controlled clinical study in patients with hematological malignancy.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xnt1ynu7s%3D&md5=9ce377c9b172179f05d013bf1fff7596CAS | 16644288PubMed |

Ferretti, C., Bruni, L., Dangles-Marie, V., Pecking, A., and Bellet, D. (2007). Molecular circuits shared by placental and cancer cells, and their implications in the proliferative, invasive and migratory capacities of trophoblasts. Hum. Reprod. Update 13, 121–141.
| Molecular circuits shared by placental and cancer cells, and their implications in the proliferative, invasive and migratory capacities of trophoblasts.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhvFWlsrw%3D&md5=09621655e7a3e85d7778d4c33a6dd18cCAS | 17068222PubMed |

Friedl, P., and Wolf, K. (2003). Tumour-cell invasion and migration: diversity and escape mechanisms. Nat. Rev. Cancer 3, 362–374.
| Tumour-cell invasion and migration: diversity and escape mechanisms.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXjtlals7o%3D&md5=a8a057cb9a74003badb238f79d0824eeCAS | 12724734PubMed |

Fuhrer, D. K., and Yang, Y. C. (1996a). Activation of Src-family protein tyrosine kinases and phosphatidylinositol 3-kinase in 3T3–L1 mouse preadipocytes by interleukin-11. Exp. Hematol. 24, 195–203.
| 1:CAS:528:DyaK28XitVyjsLc%3D&md5=00272d4a35617a46aaabb8bcbb9054b7CAS | 8641341PubMed |

Fuhrer, D. K., and Yang, Y. C. (1996b). Complex formation of JAK2 with PP2A, P13K, and in response to the hematopoietic cytokine interleukin-11. Biochem. Biophys. Res. Commun. 224, 289–296.
| Complex formation of JAK2 with PP2A, P13K, and in response to the hematopoietic cytokine interleukin-11.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28Xktl2qt70%3D&md5=21026d886ca62ba6a36f44c95487b104CAS | 8702385PubMed |

Gruslin, A., and Lemyre, B. (2011). Pre-eclampsia: fetal assessment and neonatal outcomes. Best Pract. Res. Clin. Obstet. Gynaecol. 25, 491–507.
| Pre-eclampsia: fetal assessment and neonatal outcomes.Crossref | GoogleScholarGoogle Scholar | 21474384PubMed |

Guo, Y., Xu, F., Lu, T., Duan, Z., and Zhang, Z. (2012). Interleukin-6 signaling pathway in targeted therapy for cancer. Cancer Treat. Rev. 38, 904–910.
| Interleukin-6 signaling pathway in targeted therapy for cancer.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xnsl2rtLc%3D&md5=d43d82d3c0e2a85628264787a0ce0654CAS | 22651903PubMed |

Gupta, J., Robbins, J., Jilling, T., and Seth, P. (2011). TGFbeta-dependent induction of interleukin-11 and interleukin-8 involves SMAD and p38 MAPK pathways in breast tumor models with varied bone metastases potential. Cancer Biol. Ther. 11, 311–316.
| TGFbeta-dependent induction of interleukin-11 and interleukin-8 involves SMAD and p38 MAPK pathways in breast tumor models with varied bone metastases potential.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXivFWhurc%3D&md5=ba8897d0daaa2468422c7daf2d03175cCAS | 21099351PubMed |

Hanavadi, S., Martin, T. A., Watkins, G., Mansel, R. E., and Jiang, W. G. (2006). Expression of interleukin 11 and its receptor and their prognostic value in human breast cancer. Ann. Surg. Oncol. 13, 802–808.
| Expression of interleukin 11 and its receptor and their prognostic value in human breast cancer.Crossref | GoogleScholarGoogle Scholar | 16614887PubMed |

Hanna, J., Goldman-Wohl, D., Hamani, Y., Avraham, I., Greenfield, C., Natanson-Yaron, S., Prus, D., Cohen-Daniel, L., Arnon, T. I., Manaster, I., Gazit, R., Yutkin, V., Benharroch, D., Porgador, A., Keshet, E., Yagel, S., and Mandelboim, O. (2006). Decidual NK cells regulate key developmental processes at the human fetal-maternal interface. Nat. Med. 12, 1065–1074.
| Decidual NK cells regulate key developmental processes at the human fetal-maternal interface.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XptFCltbs%3D&md5=699bd08ba25e129f5a0ce64315da93e4CAS | 16892062PubMed |

Heinrich, P. C., Behrmann, I., Haan, S., Hermanns, H. H., Müller-Newen, G., and Schaper, F. (2003). Principles of interleukin (IL)-6-type cytokine signalling and its regulation. Biochem. J. 374, 1–20.
| Principles of interleukin (IL)-6-type cytokine signalling and its regulation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXmtF2hurs%3D&md5=bf640acd79f014e547a5355b0af4c95dCAS | 12773095PubMed |

Hess, S., Rheinheimer, C., Tidow, F., Bartling, G., Kaps, C., Lauber, J., Buer, J., and Klos, A. (2001). The reprogrammed host: Chlamydia trachomatis-induced up-regulation of glycoprotein 130 cytokines, transcription factors, and antiapoptotic genes. Arthritis Rheum. 44, 2392–2401.
| The reprogrammed host: Chlamydia trachomatis-induced up-regulation of glycoprotein 130 cytokines, transcription factors, and antiapoptotic genes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XhtVei&md5=962c2f8285e985b1ca30aae5731dabe4CAS | 11665982PubMed |

Hilton, D. J., Hilton, A. A., Raicevic, A., Rakar, S., Harrison-Smith, M., Gough, N. M., Begley, C. G., Metcalf, D., Nicola, N. A., and Willson, T. A. (1994). Cloning of a murine IL-11 receptor alpha-chain; requirement for gp130 for high affinity binding and signal transduction. EMBO J. 13, 4765–4775.
| 1:CAS:528:DyaK2MXhvF2iurk%3D&md5=54447e9763661a82a91b6210958d4887CAS | 7957045PubMed |

Holtan, S. G., Creedon, D. J., Haluska, P., and Markovic, S. N. (2009). Cancer and pregnancy: parallels in growth, invasion, and immune modulation and implications for cancer therapeutic agents. Mayo Clin. Proc. 84, 985–1000.
| Cancer and pregnancy: parallels in growth, invasion, and immune modulation and implications for cancer therapeutic agents.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhsVGms7vP&md5=7fc8c0a22a133c63116b003752eaaef5CAS | 19880689PubMed |

Huppertz, B., Kertschanska, S., Demir, A. Y., Frank, H. G., and Kaufmann, P. (1997). Immunohistochemistry of matrix metalloproteinases (MMP), their substrates, and their inhibitors (TIMP) during trophoblast invasion in the human placenta. Cell Tissue Res. 291, 133–148.
| Immunohistochemistry of matrix metalloproteinases (MMP), their substrates, and their inhibitors (TIMP) during trophoblast invasion in the human placenta.Crossref | GoogleScholarGoogle Scholar |

Jemal, A., Bray, F., Center, M. M., Ferlay, J., Ward, E., and Forman, D. (2011). Global cancer statistics. CA Cancer J. Clin. 61, 69–90.
| Global cancer statistics.Crossref | GoogleScholarGoogle Scholar | 21296855PubMed |

Karpovich, N., Chobotova, K., Carver, J., Heath, J., Barlow, D., and Mardon, H. (2003). Expression and function of interleukin-11 and its receptor a in the human endometrium. Mol. Hum. Reprod. 8, 75–80.
| Expression and function of interleukin-11 and its receptor a in the human endometrium.Crossref | GoogleScholarGoogle Scholar |

Kaufmann, P., Black, S., and Huppertz, B. (2003). Endovascular trophoblast invasion: implications for the pathogenesis of intrauterine growth retardation and preeclampsia. Biol. Reprod. 69, 1–7.
| Endovascular trophoblast invasion: implications for the pathogenesis of intrauterine growth retardation and preeclampsia.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXkvFCnsbY%3D&md5=612dc655f73938a7f07ee13e2fe5253eCAS | 12620937PubMed |

Kessenbrock, K., Plaks, V., and Werb, Z. (2010). Matrix metalloproteinases: regulators of the tumor microenvironment. Cell 141, 52–67.
| Matrix metalloproteinases: regulators of the tumor microenvironment.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXlsVSgtb4%3D&md5=d98f7f6e80f95c7241b0413bbde673e8CAS | 20371345PubMed |

Koumantaki, Y., Matalliotakis, I., Sifakis, S., Kyriakou, D., Neonaki, M., Goymenou, A., and Koumantakis, E. (2001). Detection of interleukin-6, interleukin-8, and interleukin-11 in plasma from women with spontaneous abortion. Eur. J. Obstet. Gynecol. Reprod. Biol. 98, 66–71.
| Detection of interleukin-6, interleukin-8, and interleukin-11 in plasma from women with spontaneous abortion.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXmtV2mu7s%3D&md5=518190eec3d6bb15aecd1115a6d194f6CAS | 11516802PubMed |

Lay, V., Yap, J., Sonderegger, S., and Dimitriadis, E. (2012). Interleukin 11 regulates endometrial cancer cell adhesion and migration via STAT3. Int. J. Oncol. 41, 759–764.
| 1:CAS:528:DC%2BC38Xht1WltLrI&md5=0eca7fd21c2994144d98a113ccaddb56CAS | 22614117PubMed |

Lehner, R., Bobak, J., Kim, N., Shroyer, A., and Shroyer, K. (2001). Localization of telomerase hTERT protein and survivin in placenta: relation to placental development and hydatidiform mole. Obstet. Gynecol. 97, 965–970.
| Localization of telomerase hTERT protein and survivin in placenta: relation to placental development and hydatidiform mole.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXjvV2ktb4%3D&md5=0932c98180fe6faaf3eef6a795a11acfCAS | 11384704PubMed |

Lemoli, R. M., Fogli, M., Fortuna, A., Amabile, M., Zucchini, P., Grande, A., Martinelli, G., Visani, G., Ferrari, S., and Tura, S. (1995). Interleukin-11 (IL-11) acts as a synergistic factor for the proliferation of human myeloid leukaemic cells. Br. J. Haematol. 91, 319–326.
| Interleukin-11 (IL-11) acts as a synergistic factor for the proliferation of human myeloid leukaemic cells.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK28%2FislKmsw%3D%3D&md5=f903fc76f0ed35d5b2aa89f1ee03521aCAS | 8547068PubMed |

Lessey, B. A., Damjanovich, L., Coutifaris, C., Castelbaum, A., Albelda, S. M., and Buck, C. A. (1992). Integrin adhesion molecules in the human endometrium. Correlation with the normal and abnormal menstrual cycle. J. Clin. Invest. 90, 188–195.
| Integrin adhesion molecules in the human endometrium. Correlation with the normal and abnormal menstrual cycle.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK38XltVyruro%3D&md5=ec74ac6dceb035693bdc0c60e9100223CAS | 1378853PubMed |

Li, F., Ambrosini, G., Chu, E. Y., Plescia, J., Tognin, S., Marchisio, P. C., and Altieri, D. C. (1998). Control of apoptosis and mitotic spindle checkpoint by survivin. Nature 396, 580–584.
| Control of apoptosis and mitotic spindle checkpoint by survivin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXotVWns70%3D&md5=dc0c3510cffe38b42977f23ba765705aCAS | 9859993PubMed |

Li, F., Devi, Y. S., Bao, L., Mao, J., and Gibori, G. (2008). Involvement of cyclin D3, CDKN1A (p21), and BIRC5 (Survivin) in interleukin 11 stimulation of decidualization in mice. Biol. Reprod. 78, 127–133.
| Involvement of cyclin D3, CDKN1A (p21), and BIRC5 (Survivin) in interleukin 11 stimulation of decidualization in mice.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXlsl0%3D&md5=7461536c33d9516dd02ad6d635c53352CAS | 17881769PubMed |

Mahboubi, K., Li, F., Plescia, J., Kirkiles-Smith, N., Mesri, M., Du, Y., Carroll, L., Elias, J., Altieri, D., and Pober, J. (2001). Interleukin-11 up-regulates survivin expression in endothelial cells through a signal transducer and activator of transcription-3 pathway. Lab. Invest. 81, 327–334.
| Interleukin-11 up-regulates survivin expression in endothelial cells through a signal transducer and activator of transcription-3 pathway.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXivVKqsLw%3D&md5=d5caaedeea4ca70e426bbe5d1f630980CAS | 11310826PubMed |

Markman, M. (1992). Systemic therapy for gynecologic cancer. Curr. Opin. Oncol. 4, 939–945.
| Systemic therapy for gynecologic cancer.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK3s%2FptVyksA%3D%3D&md5=796c80542e6f6d4d41340b45bb23d133CAS | 1457510PubMed |

Matadeen, R., Hon, W. C., Heath, J. K., Jones, E. Y., and Fuller, S. (2007). The dynamics of signal triggering in a gp130–receptor complex. Structure 15, 441–448.
| The dynamics of signal triggering in a gp130–receptor complex.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXkt1aisr8%3D&md5=b53dce5ce519fde36ebbf0288b5d0f5eCAS | 17437716PubMed |

Menkhorst, E., Salamonsen, L. A., Robb, L., and Dimitriadis, E. (2009). IL11 antagonist inhibits uterine stromal differentiation, causing pregnancy failure in mice. Biol. Reprod. 80, 920–927.
| IL11 antagonist inhibits uterine stromal differentiation, causing pregnancy failure in mice.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXlsVWqu7g%3D&md5=bc82a72021cc0baf2d752fcfe08083f0CAS | 19144959PubMed |

Necula, L. G., Chivu-Economescu, M., Stanciulescu, E. L., Bleotu, C., Dima, S. O., Alexiu, I., Dumitru, A., Constantinescu, G., Popescu, I., and Diaconu, C. C. (2012). IL-6 and IL-11 as markers for tumor aggressiveness and prognosis in gastric adenocarcinoma patients without mutations in Gp130 subunits. J. Gastrointestin. Liver Dis. 21, 23–29.
| 22457856PubMed |

Neijt, J. P. (1994). Advances in the chemotherapy of gynecologic cancer. Curr. Opin. Oncol. 6, 531–538.
| Advances in the chemotherapy of gynecologic cancer.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK2M7islOrtA%3D%3D&md5=37e11f99304535b0f22308f1f1c52fecCAS | 7827159PubMed |

Nishina, T., Komazawa-Sakon, S., Yanaka, S., Piao, X., Zheng, D. M., Piao, J. H., Kojima, Y., Yamashina, S., Sano, E., Putoczki, T., Doi, T., Ueno, T., Ezaki, J., Ushio, H., Ernst, M., Tsumoto, K., Okumura, K., and Nakano, H. (2012). Interleukin-11 links oxidative stress and compensatory proliferation. Sci. Signal. 5, ra5.
| Interleukin-11 links oxidative stress and compensatory proliferation.Crossref | GoogleScholarGoogle Scholar | 22253262PubMed |

Paiva, P., Salamonsen, L. A., Manuelpillai, U., Walker, C., Tapia, A., Wallace, U. M., and Dimitriadis, E. (2007). Interleukin-11 promotes migration, but not proliferation, of human trophoblast cells, implying a role in placentation. Endocrinology 148, 5566–5572.
| Interleukin-11 promotes migration, but not proliferation, of human trophoblast cells, implying a role in placentation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXht1aisr7P&md5=e3f2bb93432e6b0b1c5cad276bde7916CAS | 17702845PubMed |

Paiva, P., Menkhorst, E., Salamonsen, L. A., and Dimitriadis, E. (2009a). Leukemia inhibitory factor and interleukin-11: critical regulators in the establishment of pregnancy. Cytokine Growth Factor Rev. 20, 319–328.
| Leukemia inhibitory factor and interleukin-11: critical regulators in the establishment of pregnancy.Crossref | GoogleScholarGoogle Scholar | 19647472PubMed |

Paiva, P., Salamonsen, L. A., Manuelpillai, U., and Dimitriadis, E. (2009b). Interleukin 11 inhibits human trophoblast invasion indicating a likely role in the decidual restraint of trophoblast invasion during placentation. Biol. Reprod. 80, 302–310.
| Interleukin 11 inhibits human trophoblast invasion indicating a likely role in the decidual restraint of trophoblast invasion during placentation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtFOitb8%3D&md5=a29dc04e6b7e06d089b082ded9b0de12CAS | 18987331PubMed |

Paul, S. R., Bennett, F., Calvetti, J. A., Kelleher, K., Wood, C. R., O'Hara, R. M., Leary, A. C., Sibley, B., Clark, S. C., and Williams, D. A. (1990). Molecular cloning of a cDNA encoding interleukin 11, a stromal cell-derived lymphopoietic and hematopoietic cytokine. Proc. Natl Acad. Sci. USA 87, 7512–7516.
| Molecular cloning of a cDNA encoding interleukin 11, a stromal cell-derived lymphopoietic and hematopoietic cytokine.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXhsl2gsrs%3D&md5=4a68fb9302e3a0bf80fe545640e8ceedCAS | 2145578PubMed |

Pensa, S., Regis, G., Boselli, D., Novelli, F., and Poli, V. (2009) STAT1 and STAT3 in tumorigenesis: two sides of the same coin? Available at http://www.ncbi.nlm.nih.gov/books/NBK6568/ [verified 30 March 2014].

Pignatelli, M., Ansari, T. W., Gunter, P., Liu, D., Hirano, S., Takeichi, M., Kloppel, G., and Lemoine, N. R. (1994). Loss of membranous E-cadherin expression in pancreatic cancer: correlation with lymph node metastasis, high grade, and advanced stage. J. Pathol. 174, 243–248.
| Loss of membranous E-cadherin expression in pancreatic cancer: correlation with lymph node metastasis, high grade, and advanced stage.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK2M7ptVKrtw%3D%3D&md5=f6845876878b50f5e29166894d7b6108CAS | 7884585PubMed |

Putoczki, T., and Ernst, M. (2010). More than a sidekick: the IL-6 family cytokine IL-11 links inflammation to cancer. J. Leukoc. Biol. 88, 1109–1117.
| More than a sidekick: the IL-6 family cytokine IL-11 links inflammation to cancer.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhsFGgtLzL&md5=a77d5222b9edd4d51b22cacbbb5d87abCAS | 20610798PubMed |

Putoczki, T. L., Thiem, S., Loving, A., Busuttil, R. A., Wilson, N. J., Ziegler, P. K., Nguyen, P. M., Preaudet, A., Farid, R., Edwards, K. M., Boglev, Y., Luwor, R. B., Jarnicki, A., Horst, D., Boussioutas, A., Heath, J. K., Sieber, O. M., Pleines, I., Kile, B. T., Nash, A., Greten, F. R., McKenzie, B. S., and Ernst, M. (2013). Interleukin-11 is the dominant IL-6 family cytokine during gastrointestinal tumorigenesis and can be targeted therapeutically. Cancer Cell 24, 257–271.
| Interleukin-11 is the dominant IL-6 family cytokine during gastrointestinal tumorigenesis and can be targeted therapeutically.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXht1Kgur3M&md5=eb0f743cb67791df201b71143a96619aCAS | 23948300PubMed |

Red-Horse, K., Zhou, Y., Genbacev, O., Prakobphol, A., Foulk, R., McMaster, M., and Fisher, S. J. (2004). Trophoblast differentiation during embryo implantation and formation of the maternal-fetal interface. J. Clin. Invest. 114, 744–754.
| Trophoblast differentiation during embryo implantation and formation of the maternal-fetal interface.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXnslWitbk%3D&md5=8723eabf70a968db33b3f741467a44f3CAS | 15372095PubMed |

Redman, C. W., and Sargent, I. L. (2005). Latest advances in understanding preeclampsia. Science 308, 1592–1594.
| Latest advances in understanding preeclampsia.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXltFemsbo%3D&md5=038bae55eee731cff5df383fef15e790CAS | 15947178PubMed |

Robb, L., Li, R., Hartley, L., Nandrukar, H., Koentgen, F., and Begley, C. (1998). Infertility in femal mice lacking the receptor for interleukin 11 is due to a deffective uterine response to implantation. Nat. Med. 4, 303–308.
| Infertility in femal mice lacking the receptor for interleukin 11 is due to a deffective uterine response to implantation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXhs1Kjtbo%3D&md5=ba381cee27a6fb5a0372d68f028f2454CAS | 9500603PubMed |

Ropeleski, M. J., Tang, J., Walsh-Reitz, M. M., Musch, M. W., and Chang, E. B. (2003). Interleukin-11-induced heat shock protein 25 confers intestinal epithelial-specific cytoprotection from oxidant stress. Gastroenterology 124, 1358–1368.
| Interleukin-11-induced heat shock protein 25 confers intestinal epithelial-specific cytoprotection from oxidant stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXktVSkt70%3D&md5=6dfe0bb3ad1b1f508bb4c7d9dbc2437cCAS | 12730876PubMed |

Salamonsen, L. A., Nie, G., Hannan, N. J., and Dimitriadis, E. (2009). Society for Reproductive Biology Founders’ Lecture 2009. Preparing fertile soil: the importance of endometrial receptivity. Reprod. Fertil. Dev. 21, 923–934.
| Society for Reproductive Biology Founders’ Lecture 2009. Preparing fertile soil: the importance of endometrial receptivity.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtVartbfM&md5=9e94f65c7620cf36177eb6914c024c33CAS | 19698296PubMed |

Sales, K. J., Grant, V., Cook, I. H., Maldonado-Perez, D., Anderson, R. A., Williams, A. R. W., and Jabbour, H. N. (2010). Interleukin-11 in endometrial adenocarcinoma is regulated by prostaglandin F2 alpha-F-prostanoid receptor interaction via the calcium-calcineurin-nuclear factor of activate T cells and negatively regulated by the regulator of calcineurin-1. Am. J. Pathol. 176, 435–445.
| Interleukin-11 in endometrial adenocarcinoma is regulated by prostaglandin F2 alpha-F-prostanoid receptor interaction via the calcium-calcineurin-nuclear factor of activate T cells and negatively regulated by the regulator of calcineurin-1.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhs12rtb8%3D&md5=d3c0be5ed40abd589c6c1bd30ced6685CAS | 20008143PubMed |

Schafer, Z. T., and Brugge, J. S. (2007). IL-6 involvement in epithelial cancers. J. Clin. Invest. 117, 3660–3663.
| IL-6 involvement in epithelial cancers.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhsVals7fJ&md5=cdb94061ebd9b41d80883032ffaa8182CAS | 18060028PubMed |

Seckl, M. J., Sebire, N. J., and Berkowitz, R. S. (2010). Gestational trophoblastic disease. Lancet 376, 717–729.
| Gestational trophoblastic disease.Crossref | GoogleScholarGoogle Scholar | 20673583PubMed |

Sharkey, A. M., Gardner, L., Hiby, S., Farrell, L., Apps, R., Masters, L., Goodridge, J., Lathbury, L., Stewart, C. A., Verma, S., and Moffett, A. (2008). Killer Ig-like receptor expression in uterine NK cells is biased toward recognition of HLA-C and alters with gestational age. J. Immunol. 181, 39–46.
| Killer Ig-like receptor expression in uterine NK cells is biased toward recognition of HLA-C and alters with gestational age.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXnsVGjurc%3D&md5=b465248f49ea7ba42324d782b01825c4CAS | 18566368PubMed |

Shaw, J. L. V., Dey, S. K., Critchley, H. O. D., and Horne, A. W. (2010). Current knowledge of the aetiology of human tubal ectopic pregnancy. Hum. Reprod. Update 16, 432–444.
| Current knowledge of the aetiology of human tubal ectopic pregnancy.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3cvhtlyjtg%3D%3D&md5=5be39c0488b1e8704c6519d309f18ab9CAS |

Sibai, B., Dekker, G., and Kupferminc, M. (2005). Pre-eclampsia. Lancet 365, 785–799.
| Pre-eclampsia.Crossref | GoogleScholarGoogle Scholar | 15733721PubMed |

Silva, J., Cerqueira, F., and Medeiros, R. (2014). Chlamydia trachomatis infection: implications for HPV status and cervical cancer. Arch. Gynecol. Obstet. 289, 715–723.
| Chlamydia trachomatis infection: implications for HPV status and cervical cancer.Crossref | GoogleScholarGoogle Scholar | 24346121PubMed |

Soda, H., Raymond, E., Sharma, S., Lawrence, R., Cerna, C., Gomez, L., Schaub, R., Von Hoff, D. D., and Izbicka, E. (1999). Recombinant human interleukin-11 is unlikely to stimulate the growth of the most common solid tumors. Anticancer Drugs 10, 97–102.
| Recombinant human interleukin-11 is unlikely to stimulate the growth of the most common solid tumors.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXisVCmsro%3D&md5=fbee3a41ecc6dc324fe6ac9f43102f4bCAS | 10194552PubMed |

Sonderegger, S., Yap, J., Menkhorst, E., Weston, G., Stanton, P., and Dimitriadis, E. (2011). Interleukin (IL) 11 mediates protein secretion and modification in human extravillous trophoblasts. Hum. Reprod. 26, 2841–2849.
| Interleukin (IL) 11 mediates protein secretion and modification in human extravillous trophoblasts.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXht1SiurzL&md5=7720d1ce8169712db76620b183b21fdfCAS | 21840908PubMed |

Soundararajan, R., and Jagannadha-Rao, A. (2004). Trophoblast ‘pseudo-tumorigenesis’: significance and contributory factors. Reprod. Biol. Endocrinol. 2, 15–27.
| Trophoblast ‘pseudo-tumorigenesis’: significance and contributory factors.Crossref | GoogleScholarGoogle Scholar | 15043753PubMed |

Suman, P., and Gupta, S. K. (2012). Comparative analysis of the invasion-associated genes expression pattern in first trimester trophoblastic (HTR-8/SVneo) and JEG-3 choriocarcinoma cells. Placenta 33, 874–877.
| Comparative analysis of the invasion-associated genes expression pattern in first trimester trophoblastic (HTR-8/SVneo) and JEG-3 choriocarcinoma cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhtlamtrjI&md5=f8d6c52df7f984d1795f6d63c7fc4164CAS | 22800585PubMed |

Suman, P., Poehlmann, T. G., Prakash, G. J., Markert, U. R., and Gupta, S. K. (2009). Interleukin-11 increases invasiveness of JEG-3 choriocarcinoma cells by modulating STAT3 expression. J. Reprod. Immunol. 82, 1–11.
| Interleukin-11 increases invasiveness of JEG-3 choriocarcinoma cells by modulating STAT3 expression.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtFGltbnO&md5=e056d5532ef543dcc796d10b323219e0CAS | 19716605PubMed |

Suman, P., Godbole, G., Thakur, R., Morales-Prieto, D. M., Modi, D. N., Markert, U. R., and Gupta, S. K. (2012). AP-1 transcription factors, mucin-type molecules and MMPs regulate the IL-11 mediated invasiveness of JEG-3 and HTR-8/SVneo trophoblastic cells. PLoS ONE 7, e29745.
| AP-1 transcription factors, mucin-type molecules and MMPs regulate the IL-11 mediated invasiveness of JEG-3 and HTR-8/SVneo trophoblastic cells.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XptFKqug%3D%3D&md5=fcea2a78285c4bbac8901c34c5ddeee7CAS | 22235337PubMed |

von Rango, U., Alfer, J., Kertschanska, S., Kemp, B., Muller-Newen, G., Heinrich, P. C., Beier, H. M., and Classen-Linke, I. (2004). Interleukin-11 expression: its significance in eutopic and ectopic human implantation. Mol. Hum. Reprod. 10, 783–792.
| Interleukin-11 expression: its significance in eutopic and ectopic human implantation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXovVOis7w%3D&md5=8684d2746ccb29903322559112f8d010CAS | 15465850PubMed |

Walboomers, J. M., Jacobs, M. V., Manos, M. M., Bosch, F. X., Kummer, J. A., Shah, K. V., Snijders, P. J., Peto, J., Meijer, C. J., and Munoz, N. (1999). Human papillomavirus is a necessary cause of invasive cervical cancer worldwide. J. Pathol. 189, 12–19.
| Human papillomavirus is a necessary cause of invasive cervical cancer worldwide.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DyaK1Mzot1CjsQ%3D%3D&md5=a9cdde39630621b87274c3125c358b18CAS | 10451482PubMed |

Wen, C. Y., Ito, M., Wang, H., Chen, L. D., Xu, Z. M., Matsuu, M., Shichijo, K., Nakayama, T., Nakashima, M., and Sekine, I. (2003). IL-11 up-regulates Tie-2 expression during the healing of gastric ulcers in rats. World J. Gastroenterol. 9, 788–790.
| 1:CAS:528:DC%2BD3sXjs1agtLw%3D&md5=e5feffce06459919e362e35621b01790CAS | 12679933PubMed |

White, C. A, Zhang, J. G., Salamonsen, L. A., Baca, M., Fairlie, W. D., Metcalf, D., Nicola, N. A., Robb, L., and Dimitriadis, E. (2007). Blocking LIF action in the uterus by using a PEGylated antagonist prevents implantation: a nonhormonal contraceptive strategy. Proc. Natl Acad. Sci. USA 104, 19 357–19 362.
| Blocking LIF action in the uterus by using a PEGylated antagonist prevents implantation: a nonhormonal contraceptive strategy.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXisVOjuw%3D%3D&md5=82e7ac770ce84a5ae72348a9a1b1c18cCAS |

Wu, D., Tao, J., Ding, J., Qu, P., Lu, Q., and Zhang, W. (2013). Interleukin-11, an interleukin-6-like cytokine, is a promising predictor for bladder cancer prognosis. Mol. Med. Rep. 7, 684–688.
| Interleukin-11, an interleukin-6-like cytokine, is a promising predictor for bladder cancer prognosis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhsFSmu7s%3D&md5=5c5d5080bfe4412aa97dae083ffdb89dCAS | 23179440PubMed |

Xiang, Z. L., Zeng, Z. C., Fan, J., Tang, Z. Y., and Zeng, H. Y. (2012). Expression of connective tissue growth factor and interleukin-11 in intratumoral tissue is associated with poor survival after curative resection of hepatocellular carcinoma. Mol. Biol. Rep. 39, 6001–6006.
| Expression of connective tissue growth factor and interleukin-11 in intratumoral tissue is associated with poor survival after curative resection of hepatocellular carcinoma.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XksVChtLw%3D&md5=d3b530e44037ed6ef40e89e29a1ba9aaCAS | 22205539PubMed |

Yamasaki, K., Taga, T., Hirata, Y., Yawata, H., Kawanishi, Y., Seed, B., Taniguchi, T., Hirano, T., and Kishimoto, T. (1988). Cloning and expression of the human interleukin-6 (BSF-2/IFN beta 2) receptor. Science 241, 825–828.
| Cloning and expression of the human interleukin-6 (BSF-2/IFN beta 2) receptor.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL1MXitFSmur4%3D&md5=958a2eb8d3dad2de602eb9174208449dCAS | 3136546PubMed |

Yamazumi, K., Nakayama, T., Kusaba, T., Wen, C. Y., Yoshizaki, A., Yakata, Y., Nagayasu, T., and Sekine, I. (2006). Expression of interleukin-11 and interleukin-11 receptor alpha in human colorectal adenocarcinoma; immunohistochemical analyses and correlation with clinicopathological factors. World J. Gastroenterol. 12, 317–321.
| 1:CAS:528:DC%2BD28Xis1yitrk%3D&md5=30ae1c4a6b1982cda53cdcd69985316fCAS | 16482637PubMed |

Yap, J., Salamonsen, L. A., Jobling, T., Nicholls, P., and Dimitriadis, E. (2010). Interleukin 11 is upregulated in uterine lavage and endometrial cancer cells in women with endometrial carcinoma. Reprod. Biol. Endocrinol. 8, 63–73.
| Interleukin 11 is upregulated in uterine lavage and endometrial cancer cells in women with endometrial carcinoma.Crossref | GoogleScholarGoogle Scholar | 20553623PubMed |

Yin, T., and Yang, Y. C. (1994). Mitogen-activated protein kinases and ribosomal S6 protein kinases are involved in signaling pathways shared by interleukin-11, interleukin-6, leukemia inhibitory factor, and oncostatin M in mouse 3T3–L1 cells. J. Biol. Chem. 269, 3731–3738.
| 1:CAS:528:DyaK2cXhs1Wht74%3D&md5=579d87fc4639f4388204f90f5e12c254CAS | 7508917PubMed |

Yoshizaki, A., Nakayama, T., Yamazumi, K., Yakata, Y., Taba, M., and Sekine, I. (2006). Expression of interleukin (IL)-11 and IL-11 receptor in human colorectal adenocarcinoma: IL-11 up-regulation of the invasive and proliferative activity of human colorectal carcinoma cells. Int. J. Oncol. 29, 869–876.
| 1:CAS:528:DC%2BD28XhtV2rtrvJ&md5=e4c980d5f21223d13df3d2352ef5484dCAS | 16964382PubMed |