학술논문

Evaluation of vitamin D biosynthesis and pathway target genes reveals UGT2A1/2 and EGFR polymorphisms associated with epithelial ovarian cancer in African American Women
Document Type
article
Author
Delores J. GrantAni ManichaikulAnthony J. AlbergElisa V. BanderaJill Barnholtz‐SloanMelissa BondyMichele L. CoteEllen FunkhouserPatricia G. MoormanLauren C. PeresEdward S. PetersAnn G. SchwartzPaul D. TerryXin‐Qun WangTemitope O. KekuCathrine HoyoAndrew BerchuckDale P. SandlerJack A. TaylorKatie M. O’BrienDigna R. Velez EdwardsTodd L. EdwardsAlicia Beeghly‐FadielNicolas WentzensenCeleste Leigh PearceAnna H. WuAlice S. WhittemoreValerie McGuireWeiva SiehJoseph H. RothsteinFrancesmary ModugnoRoberta NessKirsten MoysichMary Anne RossingJennifer A. DohertyThomas A. SellersJennifer B. Permuth‐WayAlvaro N. MonteiroDouglas A. LevineVeronica Wendy SetiawanChristopher A. HaimanLoic LeMarchandLynne R. WilkensBeth Y. KarlanUsha MenonSusan RamusSimon GaytherAleksandra Gentry‐MaharajKathryn L. TerryDaniel W. CramerEllen L. GoodeMelissa C. LarsonScott H. KaufmannRikki CanniotoKunle OdunsiJohn L. EtterRuea‐Yea HuangMarcus Q. BernardiniAlicia A. ToneTaymaa MayMarc T. GoodmanPamela J. ThompsonMichael E. CarneyShelley S. TworogerElizabeth M. PooleDiether LambrechtsIgnace VergoteAdriaan VandersticheleEls Van NieuwenhuysenHoda Anton‐CulverArgyrios ZiogasJames D. BrentonLine BjorgeHelga B. SalvensenLambertus A. KiemeneyLeon F. A. G. MassugerTanja PejovicAmanda BrueglMelissa MoffittLinda CookNhu D. LeAngela Brooks‐WilsonLinda E. KelemenPaul D.P. PharoahHonglin SongIan CampbellDiana EcclesAnna DeFazioCatherine J. KennedyJoellen M. Schildkraut
Source
Cancer Medicine, Vol 8, Iss 5, Pp 2503-2513 (2019)
Subject
African ancestry risk
genetic association
ovarian cancer
vitamin D pathway
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Language
English
ISSN
2045-7634
Abstract
Abstract An association between genetic variants in the vitamin D receptor (VDR) gene and epithelial ovarian cancer (EOC) was previously reported in women of African ancestry (AA). We sought to examine associations between genetic variants in VDR and additional genes from vitamin D biosynthesis and pathway targets (EGFR, UGT1A, UGT2A1/2, UGT2B, CYP3A4/5, CYP2R1, CYP27B1, CYP24A1, CYP11A1, and GC). Genotyping was performed using the custom‐designed 533,631 SNP Illumina OncoArray with imputation to the 1,000 Genomes Phase 3 v5 reference set in 755 EOC cases, including 537 high‐grade serous (HGSOC), and 1,235 controls. All subjects are of African ancestry (AA). Logistic regression was performed to estimate odds ratios (OR) and 95% confidence intervals (CI). We further evaluated statistical significance of selected SNPs using the Bayesian False Discovery Probability (BFDP). A significant association with EOC was identified in the UGT2A1/2 region for the SNP rs10017134 (per allele OR = 1.4, 95% CI = 1.2‐1.7, P = 1.2 × 10−6, BFDP = 0.02); and an association with HGSOC was identified in the EGFR region for the SNP rs114972508 (per allele OR = 2.3, 95% CI = 1.6‐3.4, P = 1.6 × 10−5, BFDP = 0.29) and in the UGT2A1/2 region again for rs1017134 (per allele OR = 1.4, 95% CI = 1.2‐1.7, P = 2.3 × 10−5, BFDP = 0.23). Genetic variants in the EGFR and UGT2A1/2 may increase susceptibility of EOC in AA women. Future studies to validate these findings are warranted. Alterations in EGFR and UGT2A1/2 could perturb enzyme efficacy, proliferation in ovaries, impact and mark susceptibility to EOC.