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膀胱癌差异甲基化基因谱的预后价值。

Prognostic value of differentially methylated gene profiles in bladder cancer.

机构信息

Department of Urology, Changhai Hospital Affiliated with Second Military Medical University, Shanghai, China.

Department of Urology, The Thrid Affiliated Hospital of Shenzhen University, Shenzhen, China.

出版信息

J Cell Physiol. 2019 Aug;234(10):18763-18772. doi: 10.1002/jcp.28515. Epub 2019 Apr 5.

Abstract

DNA methylation can regulate gene expression and is pivotal in the occurrence and development of bladder cancer. In this study, we analyzed whole-genome DNA methylation on the basis of data from The Cancer Genome Atlas to select epigenetic biomarkers predictive of survival and further understand the molecular mechanisms underlying methylation patterns in bladder cancer. We identified 540 differentially methylated genes between tumor and normal tissues, including a number of independent prognostic factors based on univariate analysis. Genes (MIR6732, SOWAHC, SERPINI1, OR10W1, OR7G3, AIM1, and ZFAND5) were integrated to establish a risk model for prognostic assessment based on multivariate Cox analysis. The methylation of SOWAHC was negatively correlated with its messenger RNA expression, and together these were significantly correlated with prognosis. This study took advantage of high-throughput data mining to provide new bioinformatics evidence and ideas for further study into the pathogenesis and prognosis of bladder cancer.

摘要

DNA 甲基化可以调节基因表达,在膀胱癌的发生和发展中起着关键作用。在这项研究中,我们基于癌症基因组图谱的数据进行全基因组 DNA 甲基化分析,选择具有生存预测能力的表观遗传生物标志物,并进一步了解膀胱癌中甲基化模式的分子机制。我们在肿瘤组织和正常组织之间鉴定出 540 个差异甲基化基因,其中包括基于单变量分析的一些独立预后因素。基于多变量 Cox 分析,我们整合基因(MIR6732、SOWAHC、SERPINI1、OR10W1、OR7G3、AIM1 和 ZFAND5)建立了一个用于预后评估的风险模型。SOWAHC 的甲基化与其信使 RNA 表达呈负相关,且两者均与预后显著相关。本研究利用高通量数据挖掘为膀胱癌的发病机制和预后提供了新的生物信息学证据和思路。

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