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H3K4 甲基化与癌症预后的关联:一项荟萃分析。

Association between H3K4 methylation and cancer prognosis: A meta-analysis.

机构信息

Department of Thoracic Surgery I, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Peking University Cancer Hospital and Institute, Beijing, China.

出版信息

Thorac Cancer. 2018 Jul;9(7):794-799. doi: 10.1111/1759-7714.12647. Epub 2018 May 8.

Abstract

BACKGROUND

Histone H3 lysine 4 methylation (H3K4 methylation), including mono-methylation (H3K4me1), di-methylation (H3K4me2), or tri-methylation (H3K4me3), is one of the epigenetic modifications to histone proteins, which are related to the transcriptional activation of genes. H3K4 methylation has both tumor inhibiting and promoting effects, and the prognostic value of H3K4 methylation in cancer remains controversial. Therefore, we performed a systematic review and meta-analysis to examine the association between H3K4 methylation and cancer prognosis.

METHODS

A comprehensive search of PubMed, Web of Science, ScienceDirect, Embase, and Ovid databases was conducted to identify studies investigating the association between H3K4 methylation and prognosis of patients with malignant tumors. The data and characteristics of each study were extracted, and the hazard ratio (HR) at a 95% confidence interval (CI) was calculated to estimate the effect.

RESULTS

A total of 1474 patients in 10 studies were enrolled in this meta-analysis. The pooled HR of 1.52 (95% CI 1.02-2.26) indicated that patients with a lower level of H3K4me2 expression were expected to have shorter overall survival, while the pooled HR of 0.45 (95% CI 0.27-0.74) indicated that patients with a lower level of H3K4me3 expression were expected to have longer overall survival.

CONCLUSION

This meta-analysis indicates that increased H3K4me3 expression and decreased H3K4me2 expression might be predictive factors of poor prognosis in cancer. Further large cohort studies are needed to confirm these findings.

摘要

背景

组蛋白 H3 赖氨酸 4 甲基化(H3K4 甲基化),包括单甲基化(H3K4me1)、二甲基化(H3K4me2)或三甲基化(H3K4me3),是组蛋白蛋白的一种表观遗传修饰,与基因的转录激活有关。H3K4 甲基化既有抑制肿瘤的作用,也有促进肿瘤的作用,H3K4 甲基化在癌症中的预后价值仍存在争议。因此,我们进行了系统评价和荟萃分析,以研究 H3K4 甲基化与癌症患者预后之间的关系。

方法

对 PubMed、Web of Science、ScienceDirect、Embase 和 Ovid 数据库进行全面检索,以确定研究 H3K4 甲基化与恶性肿瘤患者预后之间关系的研究。提取每个研究的数据和特征,并计算风险比(HR)及其 95%置信区间(CI)以估计效应。

结果

共有 10 项研究的 1474 名患者纳入本荟萃分析。荟萃分析结果显示,H3K4me2 表达水平较低的患者总生存期较短的合并 HR 为 1.52(95%CI 1.02-2.26),H3K4me3 表达水平较低的患者总生存期较长的合并 HR 为 0.45(95%CI 0.27-0.74)。

结论

本荟萃分析表明,H3K4me3 表达增加和 H3K4me2 表达减少可能是癌症不良预后的预测因素。需要进一步开展大样本队列研究来验证这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d524/6026618/37ff7cc4c15b/TCA-9-794-g003.jpg

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