Prognostic significance of N6-methyladenosine-modified related chemotransferase METTL3 in gastric carcinoma: Evidence from meta-analysis

医学 内科学 危险系数 荟萃分析 子群分析 置信区间 肿瘤科 胃肠病学 科克伦图书馆 生存分析
作者
Chenglou Zhu,Qiong Wu,Yan Xu,Jichun Ma,Yongli Hu,Junhong Wang,Zhenhua Gao,Mingxu Da
出处
期刊:International Journal of Biological Markers [SAGE Publishing]
卷期号:38 (3-4): 185-193 被引量:2
标识
DOI:10.1177/03936155231184908
摘要

Background N6-methyladenosine (m 6 A) methylation is known as the research hotspot for tumor epimodification, and its associated methyltransferase-like3 (METTL3) is significantly differentially expressed in gastric carcinoma, but its clinical value has not been summarized. This meta-analysis aimed to evaluate the prognostic significance of METTL3 in gastric carcinoma. Material and methods Databases, including PubMed, EMBASE (Ovid platform), Science Direct, Scopus, MEDLINE, Google Scholar, Web of Science, and Cochrane Library, were used to identify relevant eligible studies. The endpoints included overall survival, progression-free survival, recurrence-free survival, post-progression survival, and disease-free survival. Hazard ratios (HR) with 95% confidence intervals (CI) were used to correlate METTL3 expression with prognosis. Subgroup and sensitivity analyses were performed. Results Seven eligible studies involving 3034 gastric carcinoma patients were recruited for this meta-analysis. The analysis showed that high METTL3 expression was associated with significantly poorer overall survival (HR = 2.37, 95% CI 1.66–3.39, P < 0.01) and unfavorable disease-free survival (HR = 2.58, 95% CI 1.97–3.38, P < 0.01), as did unfavorable progression-free survival (HR = 1.48, 95% CI 1.19–1.84, P < 0.01)/recurrence-free survival (HR = 2.62, 95% CI 1.93–5.62, P < 0.01)/post-progression survival (HR = 1.53, 95% CI 1.22–1.91, P < 0.01). Subgroup analysis found that high METTL3 expression was associated with worse overall survival in patients with Chinese (HR = 2.21, 95% CI 1.48–3.29, P < 0.01), in studies with sample source from formalin-fixed, paraffin-embedded tissues (HR = 2.66, 95% CI 1.79–3.94, P < 0.01), and the reported directly from articles group (HR = 2.42, 95% CI 1.66–3.53, P < 0.01). The subgroup analysis that was performed based on sample size, detected method, and follow-up showed the same results. Conclusions High expression of METTL3 predicts poor prognosis in gastric carcinoma, indicating promise for METTL3 as a prognostic biomarker. Systematic review registration: https://www.crd.york.ac.uk/prospero , ID = CRD42023408519

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