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Risk of ovarian cancer and the NF-κB pathway: genetic association with IL1A and TNFSF10.

  • Author(s): Charbonneau, Bridget
  • Block, Matthew S
  • Bamlet, William R
  • Vierkant, Robert A
  • Kalli, Kimberly R
  • Fogarty, Zachary
  • Rider, David N
  • Sellers, Thomas A
  • Tworoger, Shelley S
  • Poole, Elizabeth
  • Risch, Harvey A
  • Salvesen, Helga B
  • Kiemeney, Lambertus A
  • Baglietto, Laura
  • Giles, Graham G
  • Severi, Gianluca
  • Trabert, Britton
  • Wentzensen, Nicolas
  • Chenevix-Trench, Georgia
  • for AOCS/ACS group
  • Whittemore, Alice S
  • Sieh, Weiva
  • Chang-Claude, Jenny
  • Bandera, Elisa V
  • Orlow, Irene
  • Terry, Kathryn
  • Goodman, Marc T
  • Thompson, Pamela J
  • Cook, Linda S
  • Rossing, Mary Anne
  • Ness, Roberta B
  • Narod, Steven A
  • Kupryjanczyk, Jolanta
  • Lu, Karen
  • Butzow, Ralf
  • Dörk, Thilo
  • Pejovic, Tanja
  • Campbell, Ian
  • Le, Nhu D
  • Bunker, Clareann H
  • Bogdanova, Natalia
  • Runnebaum, Ingo B
  • Eccles, Diana
  • Paul, James
  • Wu, Anna H
  • Gayther, Simon A
  • Hogdall, Estrid
  • Heitz, Florian
  • Kaye, Stanley B
  • Karlan, Beth Y
  • Anton-Culver, Hoda
  • Gronwald, Jacek
  • Hogdall, Claus K
  • Lambrechts, Diether
  • Fasching, Peter A
  • Menon, Usha
  • Schildkraut, Joellen
  • Pearce, Celeste Leigh
  • Levine, Douglas A
  • Kjaer, Susanne Kruger
  • Cramer, Daniel
  • Flanagan, James M
  • Phelan, Catherine M
  • Brown, Robert
  • Massuger, Leon FAG
  • Song, Honglin
  • Doherty, Jennifer A
  • Krakstad, Camilla
  • Liang, Dong
  • Odunsi, Kunle
  • Berchuck, Andrew
  • Jensen, Allan
  • Lubinski, Jan
  • Nevanlinna, Heli
  • Bean, Yukie T
  • Lurie, Galina
  • Ziogas, Argyrios
  • Walsh, Christine
  • Despierre, Evelyn
  • Brinton, Louise
  • Hein, Alexander
  • Rudolph, Anja
  • Dansonka-Mieszkowska, Agnieszka
  • Olson, Sara H
  • Harter, Philipp
  • Tyrer, Jonathan
  • Vitonis, Allison F
  • Brooks-Wilson, Angela
  • Aben, Katja K
  • Pike, Malcolm C
  • Ramus, Susan J
  • Wik, Elisabeth
  • Cybulski, Cezary
  • Lin, Jie
  • Sucheston, Lara
  • Edwards, Robert
  • McGuire, Valerie
  • Lester, Jenny
  • du Bois, Andreas
  • Lundvall, Lene
  • Wang-Gohrke, Shan
  • Szafron, Lukasz M
  • Lambrechts, Sandrina
  • Yang, Hannah
  • Beckmann, Matthias W
  • Pelttari, Liisa M
  • Van Altena, Anne M
  • van den Berg, David
  • Halle, Mari K
  • Gentry-Maharaj, Aleksandra
  • Schwaab, Ira
  • Chandran, Urmila
  • Menkiszak, Janusz
  • Ekici, Arif B
  • Wilkens, Lynne R
  • Leminen, Arto
  • Modugno, Francesmary
  • Friel, Grace
  • Rothstein, Joseph H
  • Vergote, Ignace
  • Garcia-Closas, Montserrat
  • Hildebrandt, Michelle AT
  • Sobiczewski, Piotr
  • Kelemen, Linda E
  • Pharoah, Paul DP
  • Moysich, Kirsten
  • Knutson, Keith L
  • Cunningham, Julie M
  • Fridley, Brooke L
  • Goode, Ellen L
  • et al.

Published Web Location

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC394648
No data is associated with this publication.
Abstract

A missense single-nucleotide polymorphism (SNP) in the immune modulatory gene IL1A has been associated with ovarian cancer risk (rs17561). Although the exact mechanism through which this SNP alters risk of ovarian cancer is not clearly understood, rs17561 has also been associated with risk of endometriosis, an epidemiologic risk factor for ovarian cancer. Interleukin-1α (IL1A) is both regulated by and able to activate NF-κB, a transcription factor family that induces transcription of many proinflammatory genes and may be an important mediator in carcinogenesis. We therefore tagged SNPs in more than 200 genes in the NF-κB pathway for a total of 2,282 SNPs (including rs17561) for genotype analysis of 15,604 cases of ovarian cancer in patients of European descent, including 6,179 of high-grade serous (HGS), 2,100 endometrioid, 1,591 mucinous, 1,034 clear cell, and 1,016 low-grade serous, including 23,235 control cases spanning 40 studies in the Ovarian Cancer Association Consortium. In this large population, we confirmed the association between rs17561 and clear cell ovarian cancer [OR, 0.84; 95% confidence interval (CI), 0.76-0.93; P = 0.00075], which remained intact even after excluding participants in the prior study (OR, 0.85; 95% CI, 0.75-0.95; P = 0.006). Considering a multiple-testing-corrected significance threshold of P < 2.5 × 10(-5), only one other variant, the TNFSF10 SNP rs6785617, was associated significantly with a risk of ovarian cancer (low malignant potential tumors OR, 0.85; 95% CI, 0.79-0.91; P = 0.00002). Our results extend the evidence that borderline tumors may have a distinct genetic etiology. Further investigation of how these SNPs might modify ovarian cancer associations with other inflammation-related risk factors is warranted.

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