학술논문

Cross-Cancer Genome-Wide Association Study of Endometrial Cancer and Epithelial Ovarian Cancer Identifies Genetic Risk Regions Associated with Risk of Both Cancers
Document Type
article
Author
Glubb, Dylan MThompson, Deborah JAben, Katja KHAlsulimani, AhmadAmant, FredericAnnibali, DanielaAttia, JohnBarricarte, AurelioBeckmann, Matthias WBerchuck, AndrewBermisheva, MarinaBernardini, Marcus QBischof, KatharinaBjorge, LineBodelon, ClaraBrand, Alison HBrenton, James DBrinton, Louise ABruinsma, FionaBuchanan, Daniel DBurghaus, StefanieButzow, RalfCai, HuiCarney, Michael EChanock, Stephen JChen, ChuChen, Xiao QingChen, ZhihuaCook, Linda SCunningham, Julie MDe Vivo, ImmaculatadeFazio, AnnaDoherty, Jennifer ADörk, Thilodu Bois, AndreasDunning, Alison MDürst, MatthiasEdwards, ToddEdwards, Robert PEkici, Arif BEwing, AilithFasching, Peter AFerguson, SarahFlanagan, James MFostira, FlorentiaFountzilas, GeorgeFriedenreich, Christine MGao, BoGaudet, Mia MGawełko, JanGentry-Maharaj, AleksandraGiles, Graham GGlasspool, RosalindGoodman, Marc TGronwald, JacekHarris, Holly RHarter, PhilippHein, AlexanderHeitz, FlorianHildebrandt, Michelle ATHillemanns, PeterHøgdall, EstridHøgdall, Claus KHolliday, Elizabeth GHuntsman, David GHuzarski, TomaszJakubowska, AnnaJensen, AllanJones, Michael EKarlan, Beth YKarnezis, AnthonyKelley, Joseph LKhusnutdinova, ElzaKilleen, Jeffrey LKjaer, Susanne KKlapdor, RüdigerKöbel, MartinKonopka, BozenaKonstantopoulou, IreneKopperud, Reidun KKoti, MadhuriKraft, PeterKupryjanczyk, JolantaLambrechts, DietherLarson, Melissa CLe Marchand, LoicLele, ShashikantLester, JennyLi, Andrew JLiang, DongLiebrich, ClemensLipworth, LorenLissowska, JolantaLu, LingengLu, Karen HMacciotta, AlessandraMattiello, AmaliaMay, TaymaaMcAlpine, Jessica NMcGuire, Valerie
Source
Cancer Epidemiology Biomarkers & Prevention. 30(1)
Subject
Epidemiology
Biomedical and Clinical Sciences
Health Sciences
Oncology and Carcinogenesis
Human Genome
Uterine Cancer
Genetics
Biotechnology
Ovarian Cancer
Prevention
Cancer
Rare Diseases
2.1 Biological and endogenous factors
Aetiology
Carcinoma
Ovarian Epithelial
Endometrial Neoplasms
Female
Genome-Wide Association Study
Humans
Ovarian Neoplasms
Quantitative Trait Loci
Risk Factors
OPAL Study Group
AOCS Group
Medical and Health Sciences
Biomedical and clinical sciences
Health sciences
Language
Abstract
BackgroundAccumulating evidence suggests a relationship between endometrial cancer and ovarian cancer. Independent genome-wide association studies (GWAS) for endometrial cancer and ovarian cancer have identified 16 and 27 risk regions, respectively, four of which overlap between the two cancers. We aimed to identify joint endometrial and ovarian cancer risk loci by performing a meta-analysis of GWAS summary statistics from these two cancers.MethodsUsing LDScore regression, we explored the genetic correlation between endometrial cancer and ovarian cancer. To identify loci associated with the risk of both cancers, we implemented a pipeline of statistical genetic analyses (i.e., inverse-variance meta-analysis, colocalization, and M-values) and performed analyses stratified by subtype. Candidate target genes were then prioritized using functional genomic data.ResultsGenetic correlation analysis revealed significant genetic correlation between the two cancers (rG = 0.43, P = 2.66 × 10-5). We found seven loci associated with risk for both cancers (P Bonferroni < 2.4 × 10-9). In addition, four novel subgenome-wide regions at 7p22.2, 7q22.1, 9p12, and 11q13.3 were identified (P < 5 × 10-7). Promoter-associated HiChIP chromatin loops from immortalized endometrium and ovarian cell lines and expression quantitative trait loci data highlighted candidate target genes for further investigation.ConclusionsUsing cross-cancer GWAS meta-analysis, we have identified several joint endometrial and ovarian cancer risk loci and candidate target genes for future functional analysis.ImpactOur research highlights the shared genetic relationship between endometrial cancer and ovarian cancer. Further studies in larger sample sets are required to confirm our findings.