Evidence of a genetic link between endometriosis and ovarian cancer

التفاصيل البيبلوغرافية
العنوان: Evidence of a genetic link between endometriosis and ovarian cancer
المؤلفون: Alice W. Lee, Claire Templeman, Douglas A. Stram, Jonathan Beesley, Jonathan Tyrer, Andrew Berchuck, Paul P. Pharoah, Georgia Chenevix-Trench, Celeste Leigh Pearce, Roberta B. Ness, Agnieszka Dansonka-Mieszkowska, Aleksandra Gentry-Maharaj, Alexander Hein, Alice S. Whittemore, Allan Jensen, Andreas du Bois, Angela Brooks-Wilson, Anja Rudolph, Anna Jakubowska, Anna H. Wu, Argyrios Ziogas, Arif B. Ekici, Arto Leminen, Barry Rosen, Beata Spiewankiewicz, Beth Y. Karlan, Britton Trabert, Brooke L. Fridley, C. Blake Gilks, Camilla Krakstad, Catherine M. Phelan, Cezary Cybulski, Christine Walsh, Claus Hogdall, Daniel W. Cramer, David G. Huntsman, Diana Eccles, Diether Lambrechts, Dong Liang, Douglas A. Levine, Edwin S. Iversen, Elisa V. Bandera, Elizabeth M. Poole, Ellen L. Goode, Els Van Nieuwenhuysen, Estrid Hogdall, Fiona Bruinsma, Florian Heitz, Francesmary Modugno, Graham G. Giles, Harvey A. Risch, Helen Baker, Helga B. Salvesen, Heli Nevanlinna, Hoda Anton-Culver, Honglin Song, Iain McNeish, Ian G. Campbell, Ignace Vergote, Ingo B. Runnebaum, Ingvild L. Tangen, Ira Schwaab, Jacek Gronwald, James Paul, Jan Lubinski, Jennifer A. Doherty, Jenny Chang-Claude, Jenny Lester, Joellen M. Schildkraut, John R. McLaughlin, Jolanta Lissowska, Jolanta Kupryjanczyk, Joseph L. Kelley, Joseph H. Rothstein, Julie M. Cunningham, Karen Lu, Karen Carty, Kathryn L. Terry, Katja K.H. Aben, Kirsten B. Moysich, Kristine G. Wicklund, Kunle Odunsi, Lambertus A. Kiemeney, Lara Sucheston-Campbell, Lene Lundvall, Leon F.A.G. Massuger, Liisa M. Pelttari, Linda E. Kelemen, Linda S. Cook, Line Bjorge, Lotte Nedergaard, Louise A. Brinton, Lynne R. Wilkens, Malcolm C. Pike, Marc T. Goodman, Maria Bisogna, Mary Anne Rossing, Matthias W. Beckmann, Matthias Dürst, Melissa C. Southey, Melissa Kellar, Michelle A.T. Hildebrandt, Nadeem Siddiqui, Natalia Antonenkova, Natalia Bogdanova, Nhu D. Le, Nicolas Wentzensen, Pamela J. Thompson, Patricia Harrington, Penelope M. Webb, Peter A. Fasching, Peter Hillemanns, Philipp Harter, Piotr Sobiczewski, Rachel Palmieri Weber, Ralf Butzow, Robert P. Edwards, Robert A. Vierkant, Rosalind Glasspool, Sandra Orsulic, Sandrina Lambrechts, Sara H. Olson, Shan Wang-Gohrke, Shashi Lele, Shelley S. Tworoger, Simon A. Gayther, Stacey A. Missmer, Steven A. Narod, Susan J. Ramus, Susanne K. Kjaer, Tanja Pejovic, Thilo Dörk, Ursula Eilber, Usha Menon, Valerie McGuire, Weiva Sieh, Xifeng Wu, Yukie Bean, Yurii B. Shvetsov
المصدر: Fertility and Sterility, 105, 1, pp. 35-43.e10
Fertility and Sterility, 105, 35-43.e10
سنة النشر: 2016
مصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, endocrine system diseases, Endometriosis, Genome-wide association study, Single-nucleotide polymorphism, Disease, Biology, Polymorphism, Single Nucleotide, Risk Assessment, Article, 03 medical and health sciences, Risk Factors, Internal medicine, Databases, Genetic, Genetic variation, medicine, Humans, Genetic Predisposition to Disease, Genetic testing, Ovarian Neoplasms, Gynecology, Women's cancers Radboud Institute for Molecular Life Sciences [Radboudumc 17], medicine.diagnostic_test, Case-control study, Computational Biology, Obstetrics and Gynecology, medicine.disease, female genital diseases and pregnancy complications, Women's cancers Radboud Institute for Health Sciences [Radboudumc 17], Phenotype, 030104 developmental biology, Reproductive Medicine, Case-Control Studies, Urological cancers Radboud Institute for Health Sciences [Radboudumc 15], Female, Neoplasm Grading, Ovarian cancer, Genome-Wide Association Study
الوصف: Contains fulltext : 172500.pdf (Publisher’s version ) (Closed access) OBJECTIVE: To evaluate whether endometriosis-associated genetic variation affects risk of ovarian cancer. DESIGN: Pooled genetic analysis. SETTING: University hospital. PATIENT(S): Genetic data from 46,176 participants (15,361 ovarian cancer cases and 30,815 controls) from 41 ovarian cancer studies. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): Endometriosis-associated genetic variation and ovarian cancer. RESULT(S): There was significant evidence of an association between endometriosis-related genetic variation and ovarian cancer risk, especially for the high-grade serous and clear cell histotypes. Overall we observed 15 significant burden statistics, which was three times more than expected. CONCLUSION(S): By focusing on candidate regions from a phenotype associated with ovarian cancer, we have shown a clear genetic link between endometriosis and ovarian cancer that warrants further follow-up. The functional significance of the identified regions and SNPs is presently uncertain, though future fine mapping and histotype-specific functional analyses may shed light on the etiologies of both gynecologic conditions.
وصف الملف: application/pdf
تدمد: 0015-0282
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e856617f27e3f4716b09f524c8f53d6dTest
https://hdl.handle.net/2066/172500Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....e856617f27e3f4716b09f524c8f53d6d
قاعدة البيانات: OpenAIRE