Cao Songyu, Wang Cheng, Huang Xinen, Dai Juncheng, Hu Lingmin, Liu Yao, Chen Jiaping, Ma Hongxia, Jin Guangfu, Hu Zhibin, Xu Lin, Shen Hongbing
Department of Epidemiology and Biostatistics, Modern Toxicology Laboratory of Ministry of Education, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu 210009, China;
J Biomed Res. 2013 May;27(3):231-8. doi: 10.7555/JBR.27.20130014. Epub 2013 Apr 25.
Apoptosis plays a key role in inhibiting tumor growth, progression and resistance to anti-tumor therapy. We hypothesized that genetic variants in apoptotic genes may affect the prognosis of lung cancer. To test this hypothesis, we selected 38 potentially functional single nucleotide polymorphisms (SNPs) from 12 genes (BAX, BCL2, BID, CASP3, CASP6, CASP7, CASP8, CASP9, CASP10, FAS, FASLG and MCL1) involved in apoptosis to assess their prognostic significance in lung cancer in a Chinese case cohort with 568 non-small cell lung cancer (NSCLC) patients. Thirty-five SNPs passing quality control underwent association analyses, 11 of which were shown to be significantly associated with NSCLC survival (P < 0.05). After Cox stepwise regression analyses, 3 SNPs were independently associated with the outcome of NSCLC (BID rs8190315: P = 0.003; CASP9 rs4645981: P = 0.007 and FAS rs1800682: P = 0.016). A favorable survival of NSCLC was significantly associated with the genotypes of BID rs8190315 AG/GG (adjusted HR = 0.65, 95% CI: 0.49-0.88), CASP9 rs4645981 AA (HR = 0.22, 95% CI: 0.07-0.69) and FAS rs1800682 GG (adjusted HR = 0.67, 95% CI: 0.46-0.97). Time-dependent receptor operation curve (ROC) analysis revealed that the area under curve (AUC) at year 5 was significantly increased from 0.762 to 0.819 after adding the risk score of these 3 SNPs to the clinical risk score. The remaining 32 SNPs were not significantly associated with NSCLC prognosis after adjustment for these 3 SNPs. These findings indicate that BID rs8190315, CASP9 rs4645981 and FAS rs1800682 polymorphisms in the apoptotic pathway may be involved in the prognosis of NSCLC in the Chinese population.
细胞凋亡在抑制肿瘤生长、进展及抗肿瘤治疗耐药性方面发挥着关键作用。我们推测凋亡基因中的遗传变异可能影响肺癌的预后。为验证这一假设,我们从参与细胞凋亡的12个基因(BAX、BCL2、BID、CASP3、CASP6、CASP7、CASP8、CASP9、CASP10、FAS、FASLG和MCL1)中选择了38个具有潜在功能的单核苷酸多态性(SNP),以评估它们在中国一个包含568例非小细胞肺癌(NSCLC)患者的病例队列中对肺癌预后的意义。35个通过质量控制的SNP进行了关联分析,其中11个显示与NSCLC生存显著相关(P<0.05)。经过Cox逐步回归分析,3个SNP与NSCLC的预后独立相关(BID rs8190315:P = 0.003;CASP9 rs4645981:P = 0.007;FAS rs1800682:P = 0.016)。NSCLC的良好生存与BID rs8190315的AG/GG基因型(校正HR = 0.65,95%CI:0.49 - 0.88)、CASP9 rs4645981的AA基因型(HR = 0.22,95%CI:0.07 - 0.69)和FAS rs1800682的GG基因型(校正HR = 0.67,95%CI:0.46 - 0.97)显著相关。时间依赖性受体操作曲线(ROC)分析显示,在将这3个SNP的风险评分添加到临床风险评分后,第5年的曲线下面积(AUC)从0.762显著增加到0.819。在对这3个SNP进行校正后,其余32个SNP与NSCLC预后无显著关联。这些发现表明,凋亡途径中的BID rs8190315、CASP9 rs4645981和FAS rs1800682多态性可能参与了中国人群NSCLC的预后。