Department of General Surgery, PLA Strategic Support Force Characteristic Medical Center, Beijing 100101, China.
Genet Res (Camb). 2022 Aug 17;2022:5338956. doi: 10.1155/2022/5338956. eCollection 2022.
Accumulating evidence indicates that the expression and/or variants of several genes play an essential role in the progress of colorectal cancer (CRC). The current study is a meta-analysis undertaken to estimate the prognosis and survival associated with , , , , , and genes among CRC patients.
The authors searched PubMed, EMBASE, and Science Direct for relevant reports published between 2000 and 2020 and analyzed them to determine any relationship between the (immunohistochemically/sequencing-detected) gene expression and variants of the selected genes and the survival of CRC patients.
The analysis included 34,074 patients from 64 studies. To evaluate association, hazard ratios (HRs) were estimated for overall survival (OS) or disease-free survival (DFS), with a 95% confidence interval (CIs). Pooled results showed that overexpression, mutation, or 4 loss of expression, mutations, and expression were associated with shorter OS. overexpression (HR: 0.137 (95% CI: 0.131-0.406)), loss of expression of or 4 (HR: 0.449 (95% CI: 0.146-0.753)), the mutations of (HR: 0.179 (95% CI: 0.126-0.485)), and expression (HR: 0.485 (95% CI: 0.772-0.198)) also presented risk for shorter DFS.
The present meta-analysis indicates that overexpression or underexpression and variants of , , 4, , and genes potentially acted as unfavorable biomarkers for the prognosis of CRC. The gene was not associated with prognosis.
越来越多的证据表明,几种基因的表达和/或变体在结直肠癌(CRC)的进展中起着至关重要的作用。本研究是一项荟萃分析,旨在评估CRC 患者中 、 、 、 、和 基因的表达和变体与预后和生存的关系。
作者检索了 2000 年至 2020 年期间发表的相关报告,并进行了分析,以确定选定基因的(免疫组织化学/测序检测)基因表达和变体与 CRC 患者的生存之间的任何关系。
该分析包括来自 64 项研究的 34074 名患者。为了评估相关性,使用风险比(HRs)估计总生存期(OS)或无病生存期(DFS),置信区间(CIs)为 95%。汇总结果显示,过表达、突变、或 4 表达缺失、突变和表达与 OS 缩短相关。过表达(HR:0.137(95%CI:0.131-0.406))、或 4 表达缺失(HR:0.449(95%CI:0.146-0.753))、 突变(HR:0.179(95%CI:0.126-0.485))和 表达(HR:0.485(95%CI:0.772-0.198))也与较短的 DFS 相关。
本荟萃分析表明, 、 、 4、 、和 基因的过表达或低表达以及变体可能作为 CRC 预后的不利生物标志物。 基因与预后无关。