Radiology Intervention Department, Anhui Chest Hospital, Hefei, China.
Clin Respir J. 2021 Jun;15(6):637-647. doi: 10.1111/crj.13335. Epub 2021 Feb 5.
This study was conducted to evaluate the relationship between the p73 G4C14-to-A4T14 polymorphism (hereafter, G4C14-to-A4T14) and lung cancer risk.
The studies on the relationship between G4C14-A4T14 and lung cancer risk published as of November 5, 2018, were comprehensively searched in PubMed, Embase, the Cochrane Library, the Chinese Wanfang database, China National Knowledge Infrastructure (CNKI), and China Biology Medicine (CBM). The last update was on May 24, 2019. Statistical analysis was performed using Stata 12.0.
The association between G4C14-A4T14 and lung cancer risk was analyzed in nine studies. The findings indicate no association between G4C14-to-A4T14 and lung cancer risk (allele model: OR = 0.90, 95% CI: 0.73-1.11, I = 86.0%, P = .330; dominant model: OR = 0.93, 95% CI: 0.74-1.17, I = 82.6%, P = .551; recessive model: OR = 0.75, 95% CI: 0.50-1.13, I = 75.2%, P = .165; homozygote model: OR = 0.74, 95% CI: 0.47-1.17, I = 79.6%, P = .199; heterozygote model: OR = 0.98, 95% CI: 0.80-1.21, I = 75.8%, P = .879). The heterogeneity between subgroups by cancer types and genotyping method was significantly reduced. After the deletion of suspected duplicates, no association was found between G4C14-to-A4T14 and lung cancer susceptibility.
Our meta-analysis confirms that G4C14-to-A4T14 is not significantly related to lung cancer risk.
本研究旨在评估 p73 G4C14 到 A4T14 多态性(以下简称 G4C14-A4T14)与肺癌风险之间的关系。
全面检索 PubMed、Embase、Cochrane 图书馆、万方数据库、中国知网(CNKI)和中国生物医学文献数据库(CBM)中截至 2018 年 11 月 5 日发表的关于 G4C14-A4T14 与肺癌风险关系的研究。最后一次更新时间为 2019 年 5 月 24 日。使用 Stata 12.0 进行统计分析。
9 项研究分析了 G4C14-A4T14 与肺癌风险之间的关系。结果表明,G4C14 到 A4T14 与肺癌风险之间无关联(等位基因模型:OR=0.90,95%CI:0.73-1.11,I²=86.0%,P=.330;显性模型:OR=0.93,95%CI:0.74-1.17,I²=82.6%,P=.551;隐性模型:OR=0.75,95%CI:0.50-1.13,I²=75.2%,P=.165;纯合子模型:OR=0.74,95%CI:0.47-1.17,I²=79.6%,P=.199;杂合子模型:OR=0.98,95%CI:0.80-1.21,I²=75.8%,P=.879)。通过按癌症类型和基因分型方法进行亚组分析,组间异质性显著降低。删除疑似重复项后,未发现 G4C14 到 A4T14 与肺癌易感性之间存在关联。
本荟萃分析证实,G4C14 到 A4T14 与肺癌风险无显著相关性。