Department of Epidemiology and Biostatistics and Ministry of Education (MOE) Key Lab for Modern Toxicology, School of Public Health, Nanjing Medical University, Nanjing, China.
Nat Genet. 2012 Jul 15;44(8):895-9. doi: 10.1038/ng.2351.
To find additional susceptibility loci for lung cancer, we tested promising associations from our previous genome-wide association study (GWAS) of lung cancer in the Chinese population in an extended validation sample size of 7,436 individuals with lung cancer (cases) and 7,483 controls. We found genome-wide significant (P < 5.0 × 10(-8)) evidence for three additional lung cancer susceptibility loci at 10p14 (rs1663689, close to GATA3, P = 2.84 × 10(-10)), 5q32 (rs2895680 in PPP2R2B-STK32A-DPYSL3, P = 6.60 × 10(-9)) and 20q13.2 (rs4809957 in CYP24A1, P = 1.20 × 10(-8)). We also found consistent associations for rs247008 at 5q31.1 (IL3-CSF2-P4HA2, P = 7.68 × 10(-8)) and rs9439519 at 1p36.32 (AJAP1-NPHP4, P = 3.65 × 10(-6)). Four of these loci showed evidence for interactions with smoking dose (P = 1.72 × 10(-10), P = 5.07 × 10(-3), P = 6.77 × 10(-3) and P = 4.49 × 10(-2) for rs2895680, rs4809957, rs247008 and rs9439519, respectively). These results advance our understanding of lung cancer susceptibility and highlight potential pathways that integrate genetic variants and smoking in the development of lung cancer.
为了寻找肺癌的其他易感基因座,我们在一个扩展的验证样本中,对我们之前在中国人群中进行的肺癌全基因组关联研究(GWAS)中具有前景的关联进行了测试,该样本包括 7436 名肺癌患者(病例)和 7483 名对照。我们在三个额外的肺癌易感基因座上发现了全基因组显著(P < 5.0×10(-8)) 证据,分别位于 10p14(rs1663689,接近 GATA3,P = 2.84×10(-10))、5q32(rs2895680 在 PPP2R2B-STK32A-DPYSL3 中,P = 6.60×10(-9)) 和 20q13.2(rs4809957 在 CYP24A1 中,P = 1.20×10(-8))。我们还发现 rs247008 位于 5q31.1(IL3-CSF2-P4HA2,P = 7.68×10(-8)) 和 rs9439519 位于 1p36.32(AJAP1-NPHP4,P = 3.65×10(-6)) 的一致关联。这四个基因座都显示出与吸烟剂量相互作用的证据(P = 1.72×10(-10),P = 5.07×10(-3),P = 6.77×10(-3)和 P = 4.49×10(-2),分别对应于 rs2895680、rs4809957、rs247008 和 rs9439519)。这些结果加深了我们对肺癌易感性的理解,并强调了遗传变异和吸烟在肺癌发生发展中整合的潜在途径。