作者
Jing Dong,Zhibin Hu,Chen Wu,Huan Guo,Baosen Zhou,Jiachun Lv,Daru Lu,Kexin Chen,Yongyong Shi,Minjie Chu,Cheng Wang,Ruyang Zhang,Juncheng Dai,Yue Jiang,Songyu Cao,Zhenzhen Qin,Dianke Yu,Hongxia Ma,Guangfu Jin,Jianhang Gong,Chongqi Sun,Xueying Zhao,Zhihua Yin,Lei Yang,Zhiqiang Li,Qifei Deng,Jiucun Wang,Wei Wu,Hong Zheng,Guoquan Zhou,Hongyan Chen,Peng Guan,Zhihang Peng,Yijiang Chen,Yongqian Shu,Lin Xu,Xiangyang Liu,Li Liu,Pin Xu,Baohui Han,Chunxue Bai,Yuxia Zhao,Haibo Zhang,Ying Yan,Christopher I. Amos,Feng Chen,Wen Tan,Jin Li,Tangchun Wu,Dongxin Lin,Hongbing Shen
摘要
Hongbing Shen and colleagues identify three new susceptibility loci for lung cancer in the Chinese population. Their follow-up analyses suggest that two of these loci interact multiplicatively with smoking dose to influence lung cancer risk. To find additional susceptibility loci for lung cancer, we tested promising associations from our previous genome-wide association study (GWAS)1 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.