Wang Yuhan, Han Yingying, Weng Qiang, Yuan Zhengrong
College of Biological Sciences and Technology, Beijing Forestry University, Beijing 100083, People's Republic of China.
Oncotarget. 2016 Oct 4;7(40):65770-65781. doi: 10.18632/oncotarget.11664.
The Xeroderma pigmentosum complementation group G (XPG) rs2296147T>C polymorphism is suspected to associate with the clinical outcomes of cancer patients. However, the results are inconsistent. This meta-analysis aimed to evaluate the reliable predictive value of XPG rs2296147T>C polymorphism on clinical outcomes of cancer patients. A total of 11 eligible studies were enrolled in this meta-analysis. Our results indicated that the cancer patients with TT and CT genotypes were significantly associated with better respond rates when compared with the CC genotype (TT versus (vs.) CC: odds ratio (OR) = 2.05, 95% confidence intervals (CIs), 1.32-3.20, P = 0.002; TT+CT vs. CC: OR= 1.57, 95% CI, 1.14-2.17, P = 0.005). The TT genotype and/or T allele might be associated with higher survival time for cancer patients than the CC genotype and/or C allele. The cumulative meta-analyses showed an apparent beneficial objective response of TT genotype on cancer patients. In conclusion, this meta-analysis suggests that the XPG rs2296147T>C polymorphism is associated with the clinical outcomes of cancer patients. The XPG rs2296147T>C polymorphism might be a predictive factor of prognosis in cancers patients and contribute to individual treatment in the future.
着色性干皮病互补组G(XPG)基因rs2296147T>C多态性被怀疑与癌症患者的临床结局相关。然而,结果并不一致。本荟萃分析旨在评估XPG rs2296147T>C多态性对癌症患者临床结局的可靠预测价值。本荟萃分析共纳入11项符合条件的研究。我们的结果表明,与CC基因型相比,TT和CT基因型的癌症患者的缓解率显著更高(TT与CC相比:优势比(OR)=2.05,95%置信区间(CI)为1.32 - 3.20,P = 0.002;TT + CT与CC相比:OR = 1.57,95%CI为1.14 - 2.17,P = 0.005)。与CC基因型和/或C等位基因相比,TT基因型和/或T等位基因可能与癌症患者更长的生存时间相关。累积荟萃分析显示TT基因型对癌症患者有明显的有益客观反应。总之,本荟萃分析表明XPG rs2296147T>C多态性与癌症患者的临床结局相关。XPG rs2296147T>C多态性可能是癌症患者预后的一个预测因素,并有助于未来的个体化治疗。