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EZH2和H3K27me3的异常过表达是食管鳞状细胞癌患者预后不良的生物标志物。

Aberrant overexpression of EZH2 and H3K27me3 serves as poor prognostic biomarker for esophageal squamous cell carcinoma patients.

作者信息

Liu Fei, Gu Lina, Cao Yu, Fan Xiaojie, Zhang Fengjuan, Sang Meixiang

机构信息

a Tumor Research Institute .

b Research Center , and.

出版信息

Biomarkers. 2016;21(1):80-90. doi: 10.3109/1354750X.2015.1118537. Epub 2015 Dec 3.

Abstract

It has been reported that the trimethylation of histone 3 on lysine 27 (H3K27me3) is required for enhancer of zeste homology 2 (EZH2)-mediated repression of various genes essential for tumorigenesis and tumor development. Here, we reported the expression of EZH2 and H3K27me3 in esophageal squamous cell carcinoma (ESCC) specimens was higher than the pericarcinoma esophageal specimens. Their expression was positively associated with the poor prognosis of ESCC patients. EZH2 expression, histological grade and distant lymph node metastasis were all independent factors for poor prognosis of ESCC. In addition, enforced expression of EZH2 in esophageal cancer-derived cells could increase the overall H3K27me3 level. Our results suggested the expression of EZH2 and H3K27me3 could serve as biomarkers in the prediction of ESCC patients' survival and ESCC metastasis.

摘要

据报道,组蛋白3赖氨酸27位点的三甲基化(H3K27me3)对于增强子结合蛋白2(EZH2)介导的对肿瘤发生和肿瘤发展所必需的各种基因的抑制作用是必需的。在此,我们报道了食管鳞状细胞癌(ESCC)标本中EZH2和H3K27me3的表达高于癌旁食管标本。它们的表达与ESCC患者的不良预后呈正相关。EZH2表达、组织学分级和远处淋巴结转移均为ESCC不良预后的独立因素。此外,在食管癌来源的细胞中强制表达EZH2可增加整体H3K27me3水平。我们的结果表明,EZH2和H3K27me3的表达可作为预测ESCC患者生存和ESCC转移的生物标志物。

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