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TERT基因中rs2853669与人类癌症风险及预后的关联:一项系统评价与荟萃分析

Association between rs2853669 in TERT gene and the risk and prognosis of human cancer: a systematic review and meta-analysis.

作者信息

Shen Na, Lu Yanjun, Wang Xiong, Peng Jing, Zhu Yaowu, Cheng Liming

机构信息

Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

出版信息

Oncotarget. 2017 Feb 7;8(31):50864-50872. doi: 10.18632/oncotarget.15140. eCollection 2017 Aug 1.

Abstract

The polymorphism rs2853669 within the promoter of telomerase reverse transcriptase gene () has been debated about its role in cancer risk and prognosis. Additionally, several studies report inconsistent results concerning the modifying effect of rs2853669 on the prognostic value of mutations in cancer patients. Here, we performed this meta-analysis to comprehensively evaluate the role of rs2853669 in the risk and prognosis of human cancer, and further assess its modifying impact on mutations in the survival of cancer patients. We systematically searched literature via PubMed, Web of Science, and EMBASE through July 2016, and included 22 eligible studies. The overall analysis (64,119 cases and 78,988 controls) demonstrated that rs2853669 did not increase or decrease the overall cancer risk. Subsequent analyses also did not reveal any association between rs2853669 and overall cancer prognosis. However, we identified a modifying effect of rs2853669 on mutations in that, among cancer patients with mutations, only those carrying the TT genotype had a poor survival (Hazard ratio = 1.56, 95% confidence interval = 1.06-2.28); subgroup analyses by cancer type also supported these results. In conclusion, our findings suggest that rs2853669 could be important for assessing the prognostic value of mutations. Future large studies are required to further validate our results.

摘要

端粒酶逆转录酶基因()启动子区域的多态性rs2853669在癌症风险和预后中的作用一直存在争议。此外,几项研究报告了关于rs2853669对癌症患者中突变预后价值的修饰作用的不一致结果。在此,我们进行了这项荟萃分析,以全面评估rs2853669在人类癌症风险和预后中的作用,并进一步评估其对癌症患者生存中突变的修饰影响。我们通过PubMed、科学网和EMBASE系统检索了截至2016年7月的文献,并纳入了22项符合条件的研究。总体分析(64119例病例和78988例对照)表明,rs2853669并未增加或降低总体癌症风险。后续分析也未发现rs2853669与总体癌症预后之间存在任何关联。然而,我们发现rs2853669对突变有修饰作用,即在携带突变的癌症患者中,只有那些携带TT基因型的患者生存情况较差(风险比=1.56,95%置信区间=1.06-2.28);按癌症类型进行的亚组分析也支持了这些结果。总之,我们的研究结果表明,rs2853669对于评估突变的预后价值可能很重要。未来需要进行大规模研究以进一步验证我们的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a75/5584211/9ef7b94de7b5/oncotarget-08-50864-g001.jpg

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