Seow Wei Jie, Matsuo Keitaro, Hsiung Chao Agnes, Shiraishi Kouya, Song Minsun, Kim Hee Nam, Wong Maria Pik, Hong Yun-Chul, Hosgood H Dean, Wang Zhaoming, Chang I-Shou, Wang Jiu-Cun, Chatterjee Nilanjan, Tucker Margaret, Wei Hu, Mitsudomi Tetsuya, Zheng Wei, Kim Jin Hee, Zhou Baosen, Caporaso Neil E, Albanes Demetrius, Shin Min-Ho, Chung Lap Ping, An She-Juan, Wang Ping, Zheng Hong, Yatabe Yasushi, Zhang Xu-Chao, Kim Young Tae, Shu Xiao-Ou, Kim Young-Chul, Bassig Bryan A, Chang Jiang, Ho James Chung Man, Ji Bu-Tian, Kubo Michiaki, Daigo Yataro, Ito Hidemi, Momozawa Yukihide, Ashikawa Kyota, Kamatani Yoichiro, Honda Takayuki, Sakamoto Hiromi, Kunitoh Hideo, Tsuta Koji, Watanabe Shun-Ichi, Nokihara Hiroshi, Miyagi Yohei, Nakayama Haruhiko, Matsumoto Shingo, Tsuboi Masahiro, Goto Koichi, Yin Zhihua, Shi Jianxin, Takahashi Atsushi, Goto Akiteru, Minamiya Yoshihiro, Shimizu Kimihiro, Tanaka Kazumi, Wu Tangchun, Wei Fusheng, Wong Jason Y Y, Matsuda Fumihiko, Su Jian, Kim Yeul Hong, Oh In-Jae, Song Fengju, Lee Victor Ho Fun, Su Wu-Chou, Chen Yuh-Min, Chang Gee-Chen, Chen Kuan-Yu, Huang Ming-Shyan, Yang Pan-Chyr, Lin Hsien-Chih, Xiang Yong-Bing, Seow Adeline, Park Jae Yong, Kweon Sun-Seog, Chen Chien-Jen, Li Haixin, Gao Yu-Tang, Wu Chen, Qian Biyun, Lu Daru, Liu Jianjun, Jeon Hyo-Sung, Hsiao Chin-Fu, Sung Jae Sook, Tsai Ying-Huang, Jung Yoo Jin, Guo Huan, Hu Zhibin, Wang Wen-Chang, Chung Charles C, Lawrence Charles, Burdett Laurie, Yeager Meredith, Jacobs Kevin B, Hutchinson Amy, Berndt Sonja I, He Xingzhou, Wu Wei, Wang Junwen, Li Yuqing, Choi Jin Eun, Park Kyong Hwa, Sung Sook Whan, Liu Li, Kang Chang Hyun, Hu Lingmin, Chen Chung-Hsing, Yang Tsung-Ying, Xu Jun, Guan Peng, Tan Wen, Wang Chih-Liang, Sihoe Alan Dart Loon, Chen Ying, Choi Yi Young, Hung Jen-Yu, Kim Jun Suk, Yoon Ho-Il, Cai Qiuyin, Lin Chien-Chung, Park In Kyu, Xu Ping, Dong Jing, Kim Christopher, He Qincheng, Perng Reury-Perng, Chen Chih-Yi, Vermeulen Roel, Wu Junjie, Lim Wei-Yen, Chen Kun-Chieh, Chan John K C, Chu Minjie, Li Yao-Jen, Li Jihua, Chen Hongyan, Yu Chong-Jen, Jin Li, Lo Yen-Li, Chen Ying-Hsiang, Fraumeni Joseph F, Liu Jie, Yamaji Taiki, Yang Yang, Hicks Belynda, Wyatt Kathleen, Li Shengchao A, Dai Juncheng, Ma Hongxia, Jin Guangfu, Song Bao, Wang Zhehai, Cheng Sensen, Li Xuelian, Ren Yangwu, Cui Ping, Iwasaki Motoki, Shimazu Taichi, Tsugane Shoichiro, Zhu Junjie, Jiang Gening, Fei Ke, Wu Guoping, Chien Li-Hsin, Chen Hui-Ling, Su Yu-Chun, Tsai Fang-Yu, Chen Yi-Song, Yu Jinming, Stevens Victoria L, Laird-Offringa Ite A, Marconett Crystal N, Lin Dongxin, Chen Kexin, Wu Yi-Long, Landi Maria Teresa, Shen Hongbing, Rothman Nathaniel, Kohno Takashi, Chanock Stephen J, Lan Qing
Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.
Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore.
Hum Mol Genet. 2017 Jan 15;26(2):454-465. doi: 10.1093/hmg/ddw414.
To evaluate associations by EGFR mutation status for lung adenocarcinoma risk among never-smoking Asian women, we conducted a meta-analysis of 11 loci previously identified in genome-wide association studies (GWAS). Genotyping in an additional 10,780 never-smoking cases and 10,938 never-smoking controls from Asia confirmed associations with eight known single nucleotide polymorphisms (SNPs). Two new signals were observed at genome-wide significance (P < 5 × 10-8), namely, rs7216064 (17q24.3, BPTF), for overall lung adenocarcinoma risk, and rs3817963 (6p21.3, BTNL2) which is specific to cases with EGFR mutations. In further sub-analyses by EGFR status, rs9387478 (ROS1/DCBLD1) and rs2179920 (HLA-DPB1) showed stronger estimated associations in EGFR-positive compared to EGFR-negative cases. Comparison of the overall associations with published results in Western populations revealed that the majority of these findings were distinct, underscoring the importance of distinct contributing factors for smoking and non-smoking lung cancer. Our results extend the catalogue of regions associated with lung adenocarcinoma in non-smoking Asian women and highlight the importance of how the germline could inform risk for specific tumour mutation patterns, which could have important translational implications.
为了评估从不吸烟的亚洲女性中表皮生长因子受体(EGFR)突变状态与肺腺癌风险之间的关联,我们对之前在全基因组关联研究(GWAS)中确定的11个基因座进行了荟萃分析。对另外10780例从不吸烟的病例和10938例从不吸烟的亚洲对照进行基因分型,证实了与8个已知单核苷酸多态性(SNP)的关联。在全基因组显著性水平(P < 5×10-8)观察到两个新信号,即rs7216064(17q24.3,BPTF)与总体肺腺癌风险相关,以及rs3817963(6p21.3,BTNL2)与EGFR突变病例特异性相关。在按EGFR状态进行的进一步亚组分析中,与EGFR阴性病例相比,rs9387478(ROS1/DCBLD1)和rs2179920(HLA-DPB1)在EGFR阳性病例中显示出更强的估计关联。将总体关联与西方人群已发表的结果进行比较,发现这些发现中的大多数是不同的,这突出了吸烟和非吸烟肺癌不同促成因素的重要性。我们的结果扩展了与从不吸烟的亚洲女性肺腺癌相关区域的目录,并强调了种系如何为特定肿瘤突变模式的风险提供信息的重要性,这可能具有重要的转化意义。