Jiang Chaowen, Yu Shilong, Qian Pin, Guo Ruiling, Zhang Ruijie, Ao Zhi, Li Qi, Wu Guoming, Chen Yan, Li Jin, Wang Changzheng, Yao Wei, Xu Jiancheng, Qian Guisheng, Ji Fuyun
Institute of Human Respiratory Disease, Xinqiao Hospital, The Third Military Medical University, Chongqing 400037, China.
Department of Respiratory Diseases, 324th Hospital of People's Liberation Army (No.324 Hospital of PLA), Chongqing 400020, China.
Oncotarget. 2016 Sep 13;7(37):59742-59753. doi: 10.18632/oncotarget.10874.
It has been well established that besides environmental factors, genetic factors are also associated with lung cancer risk. However, to date, the prior identified genetic variants and loci only explain a small fraction of the familial risk of lung cancer. Hence it is vital to investigate the remaining missing heritability to understand the development and process of lung cancer. In the study, to test our hypothesis that the previously identified breast cancer risk-associated genetic polymorphisms at the TOX3/LOC643714 locus might contribute to lung cancer risk, 16 SNPs at the TOX3/LOC643714 locus were evaluated in a Han Chinese population based on a case-control study. Pearson's chi-square test or Fisher's exact test revealed that rs9933638, rs12443621, and rs3104746 were significantly associated with lung cancer risk (P < 0.001, P < 0.001, and P = 0.005, respectively). Logistic regression analyses displayed that lung cancer risk of individuals with rs9933638(GG+GA) were 1.89 times higher than that of rs9933638AA carriers (OR = 1.893, 95% CI = 1.308-2.741, P = 0.001). Similar findings were manifested for rs12443621 (OR = 1.824, 95% CI = 1.272-2.616, P = 0.001, rs12443621(GG+GA) carriers vs. rs12443621AA carriers) and rs3104746 (OR = 1.665, 95% CI = 1.243-2.230, P = 0.001, rs3104746TT carriers vs. rs3104746(TA+AA) carriers). The study discovered for the first time that three SNPs (rs9933638, rs12443621, and rs3104746) at the TOX3/LOC643714 locus contributed to lung cancer risk, providing new evidences that lung cancer and breast cancer are linked at the molecular and genetic level to a certain extent.
众所周知,除环境因素外,遗传因素也与肺癌风险相关。然而,迄今为止,先前已确定的基因变异和基因座仅解释了肺癌家族风险的一小部分。因此,研究剩余的缺失遗传度对于了解肺癌的发生和发展过程至关重要。在本研究中,为了验证我们的假设,即在TOX3/LOC643714基因座上先前确定的与乳腺癌风险相关的基因多态性可能与肺癌风险有关,我们基于病例对照研究在汉族人群中评估了TOX3/LOC643714基因座上的16个单核苷酸多态性(SNP)。Pearson卡方检验或Fisher精确检验显示,rs9933638、rs12443621和rs3104746与肺癌风险显著相关(P分别<0.001、<0.001和 = 0.005)。逻辑回归分析显示,rs9933638(GG + GA)个体的肺癌风险比rs9933638 AA携带者高1.89倍(OR = 1.893,95% CI = 1.308 - 2.741,P = 0.001)。rs12443621(OR = 1.824,95% CI = 1.272 - 2.616,P = 0.001,rs12443621(GG + GA)携带者与rs12443621 AA携带者相比)和rs3104746(OR = 1.665,95% CI = 1.243 - 2.230,P = 0.001,rs3104746 TT携带者与rs3104746(TA + AA)携带者相比)也有类似发现。该研究首次发现TOX3/LOC643714基因座上的三个SNP(rs9933638、rs12443621和rs3104746)与肺癌风险有关,为肺癌和乳腺癌在分子和遗传水平上在一定程度上存在联系提供了新证据。