Institute of Digestive Endoscopy and Medical Centre for Digestive Disease, The Second Affiliated Hospital, Nanjing Medical University, Nanjing, Jiangsu Province, 210011, People's Republic of China.
BMC Cancer. 2020 Sep 9;20(1):866. doi: 10.1186/s12885-020-07346-7.
An increasing number of studies have described the aberrant expression of homeobox (HOX) proteins in gastric cancer (GC), which is critically associated with the prognosis and clinicopathological characteristics of GC. This study was conducted to investigate the clinical value and action mechanisms of HOX proteins in GC.
A comprehensive search of PubMed, Embase, Web of Science and Cochrane Library was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) statement. The pooled hazard ratio (HR) with its 95% confidence interval (95% CI) and the pooled odds ratio (OR) with its 95% CI were used to assess the effect of HOX protein expression on the prognosis and clinicopathological features of GC, respectively.
Nineteen studies containing 3775 patients were selected for this study. Heterogeneity among HRs of overall survival (OS) was markedly high (I = 90.5%, p = 0.000). According to the subgroup analysis, increased expression of HOX protein in the downregulated subgroup was associated with a good prognosis for patients with GC (pooled HR: 0.46, 95% CI: 0.36-0.59, I = 3.1%, p = 0.377), while overexpression of HOX protein in the upregulated subgroup was correlated with a reduced OS (pooled HR: 2.59, 95% CI: 1.79-3.74, I = 73.5%, p = 0.000). The aberrant expression of HOX protein was crucially related to the TNM stage, depth of tumour invasion, tumour size, lymph node metastasis, distant metastasis, vascular invasion, histological differentiation and Lauren classification in patients with GC. In addition, the molecular mechanisms by which HOX proteins regulate tumorigenesis and development of GC were also explored.
HOX proteins play vital roles in GC progression, which might serve as prognostic markers and therapeutic targets for GC.
越来越多的研究描述了同源盒(HOX)蛋白在胃癌(GC)中的异常表达,这与 GC 的预后和临床病理特征密切相关。本研究旨在探讨 HOX 蛋白在 GC 中的临床价值和作用机制。
根据系统评价和荟萃分析的首选报告项目(PRISMA)声明,对 PubMed、Embase、Web of Science 和 Cochrane Library 进行了全面检索。使用合并的风险比(HR)及其 95%置信区间(95%CI)和合并的优势比(OR)及其 95%CI 分别评估 HOX 蛋白表达对 GC 预后和临床病理特征的影响。
本研究共纳入 19 项研究,包含 3775 例患者。总生存(OS)的 HR 异质性非常高(I=90.5%,p=0.000)。根据亚组分析,下调亚组中 HOX 蛋白表达增加与 GC 患者的良好预后相关(合并 HR:0.46,95%CI:0.36-0.59,I=3.1%,p=0.377),而上调亚组中 HOX 蛋白的过表达与 OS 降低相关(合并 HR:2.59,95%CI:1.79-3.74,I=73.5%,p=0.000)。HOX 蛋白的异常表达与 GC 患者的 TNM 分期、肿瘤浸润深度、肿瘤大小、淋巴结转移、远处转移、血管侵犯、组织学分化和 Lauren 分类密切相关。此外,还探讨了 HOX 蛋白调节 GC 发生和发展的分子机制。
HOX 蛋白在 GC 进展中发挥着重要作用,它们可能成为 GC 的预后标志物和治疗靶点。