Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Division of Research, Kaiser Permanente Northern California, Oakland, California.
Clin Cancer Res. 2017 Dec 15;23(24):7550-7557. doi: 10.1158/1078-0432.CCR-17-1401. Epub 2017 Oct 3.
DNA topoisomerase inhibitors are commonly used for treating small-cell lung cancer (SCLC). Tyrosyl-DNA phosphodiesterase (TDP1) repairs DNA damage caused by this class of drugs and may therefore influence treatment outcome. In this study, we investigated whether common single-nucleotide polymorphisms (SNP) are associated with overall survival among SCLC patients. Two SNPs (rs942190 and rs2401863) were analyzed in 890 patients from 10 studies in the International Lung Cancer Consortium (ILCCO). The Kaplan-Meier method and Cox regression analyses were used to evaluate genotype associations with overall mortality at 36 months postdiagnosis, adjusting for age, sex, race, and tumor stage. Patients homozygous for the minor allele (GG) of rs942190 had poorer survival compared with those carrying AA alleles, with a HR of 1.36 [95% confidence interval (CI): 1.08-1.72, = 0.01), but no association with survival was observed for patients carrying the AG genotype (HR = 1.04, 95% CI, 0.84-1.29, = 0.72). For rs2401863, patients homozygous for the minor allele (CC) tended to have better survival than patients carrying AA alleles (HR = 0.79; 95% CI, 0.61-1.02, = 0.07). Results from the Genotype Tissue Expression (GTEx) Project, the Encyclopedia of DNA Elements (ENCODE), and the ePOSSUM web application support the potential function of rs942190. We found the rs942190 GG genotype to be associated with relatively poor survival among SCLC patients. Further investigation is needed to confirm the result and to determine whether this genotype may be a predictive marker for treatment efficacy of DNA topoisomerase inhibitors. .
DNA 拓扑异构酶抑制剂常用于治疗小细胞肺癌 (SCLC)。酪氨酰-DNA 磷酸二酯酶 (TDP1) 修复此类药物引起的 DNA 损伤,因此可能影响治疗效果。在这项研究中,我们调查了常见的单核苷酸多态性 (SNP) 是否与 SCLC 患者的总生存相关。在国际肺癌联合会 (ILCCO) 的 10 项研究中,对 890 名患者的 2 个 SNP(rs942190 和 rs2401863) 进行了分析。使用 Kaplan-Meier 方法和 Cox 回归分析来评估基因型与诊断后 36 个月总体死亡率的相关性,调整年龄、性别、种族和肿瘤分期。与携带 AA 等位基因的患者相比,rs942190 中的次要等位基因 (GG) 纯合子患者的生存较差,HR 为 1.36 [95%置信区间 (CI):1.08-1.72, = 0.01),但未观察到携带 AG 基因型的患者与生存相关 (HR = 1.04,95% CI,0.84-1.29, = 0.72)。对于 rs2401863,与携带 AA 等位基因的患者相比,携带 CC 等位基因的患者的生存趋势较好 (HR = 0.79;95% CI,0.61-1.02, = 0.07)。基因型组织表达 (GTEx) 项目、DNA 元素百科全书 (ENCODE) 和 ePOSSUM 网络应用程序的结果支持 rs942190 的潜在功能。我们发现 rs942190 GG 基因型与 SCLC 患者的生存较差相关。需要进一步的研究来确认结果,并确定这种基因型是否可能成为 DNA 拓扑异构酶抑制剂治疗效果的预测标志物。