Section of Genetics, Genetic Epidemiology Group, International Agency for Research on Cancer, World Health Organization, Lyon, France.
Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America.
PLoS Genet. 2021 Mar 5;17(3):e1009254. doi: 10.1371/journal.pgen.1009254. eCollection 2021 Mar.
Squamous cell carcinomas (SqCC) of the aerodigestive tract have similar etiological risk factors. Although genetic risk variants for individual cancers have been identified, an agnostic, genome-wide search for shared genetic susceptibility has not been performed. To identify novel and pleotropic SqCC risk variants, we performed a meta-analysis of GWAS data on lung SqCC (LuSqCC), oro/pharyngeal SqCC (OSqCC), laryngeal SqCC (LaSqCC) and esophageal SqCC (ESqCC) cancers, totaling 13,887 cases and 61,961 controls of European ancestry. We identified one novel genome-wide significant (Pmeta<5x10-8) aerodigestive SqCC susceptibility loci in the 2q33.1 region (rs56321285, TMEM273). Additionally, three previously unknown loci reached suggestive significance (Pmeta<5x10-7): 1q32.1 (rs12133735, near MDM4), 5q31.2 (rs13181561, TMEM173) and 19p13.11 (rs61494113, ABHD8). Multiple previously identified loci for aerodigestive SqCC also showed evidence of pleiotropy in at least another SqCC site, these include: 4q23 (ADH1B), 6p21.33 (STK19), 6p21.32 (HLA-DQB1), 9p21.33 (CDKN2B-AS1) and 13q13.1(BRCA2). Gene-based association and gene set enrichment identified a set of 48 SqCC-related genes rel to DNA damage and epigenetic regulation pathways. Our study highlights the importance of cross-cancer analyses to identify pleiotropic risk loci of histology-related cancers arising at distinct anatomical sites.
头颈部鳞状细胞癌(SqCC)具有相似的病因危险因素。虽然已经确定了个别癌症的遗传风险变异体,但尚未进行针对遗传易感性的全基因组、无偏倚搜索。为了确定新的、多效性的 SqCC 风险变异体,我们对肺 SqCC(LuSqCC)、口咽/咽 SqCC(OSqCC)、喉 SqCC(LaSqCC)和食管 SqCC(ESqCC)癌症的 GWAS 数据进行了荟萃分析,共纳入了 13887 例欧洲血统的病例和 61961 例对照。我们在 2q33.1 区域(rs56321285,TMEM273)发现了一个新的全基因组显著(Pmeta<5x10-8)的 aerodigestive SqCC 易感性位点。此外,还有三个以前未知的位点达到了提示性显著水平(Pmeta<5x10-7):1q32.1(rs12133735,靠近 MDM4)、5q31.2(rs13181561,TMEM173)和 19p13.11(rs61494113,ABHD8)。多个先前鉴定的 aerodigestive SqCC 位点在至少另一个 SqCC 部位也显示出多效性的证据,这些包括:4q23(ADH1B)、6p21.33(STK19)、6p21.32(HLA-DQB1)、9p21.33(CDKN2B-AS1)和 13q13.1(BRCA2)。基于基因的关联和基因集富集鉴定了一组与 DNA 损伤和表观遗传调控途径相关的 48 个 SqCC 相关基因。我们的研究强调了跨癌症分析对于鉴定具有不同解剖部位的组织学相关癌症的多效性风险位点的重要性。