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HACE1基因启动子的去甲基化抑制人肝癌细胞的增殖。

Demethylation of the HACE1 gene promoter inhibits the proliferation of human liver cancer cells.

作者信息

Yu Zhijun, Li Yinyin, Han Tao, Liu Zhaozhe

机构信息

Department of 2016 Levels of Integrated Traditional Chinese and Western Medicine Clinical Oncology, Liaoning University of Traditional Chinese Medicine Graduate School, Shenyang, Liaoning 110847, P.R. China.

Oncology Diagnosis and Treatment Center, General Hospital of Shenyang Military Area Command, Shenyang, Liaoning 110016, P.R. China.

出版信息

Oncol Lett. 2019 May;17(5):4361-4368. doi: 10.3892/ol.2019.10139. Epub 2019 Mar 12.

Abstract

HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 (HACE1) is frequently downregulated or lost in numerous types of cancer, including liver cancer. The aim of the present study was to examine whether demethylation of the HACE1 gene could inhibit tumour progression. The expression of HACE1 was detected in liver cancer cell lines. Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated (Cas)-based demethylation single guide RNAs for the HACE1 gene promoter were designed and transfected into liver cancer cells. Subsequently, proliferation was detected by MTT and colony formation assays, and optineurin (OPTN) ubiquitination and microtubule-associated proteins 1A/1B light chain 3B protein levels were detected by immunoblotting. The levels of HACE1 were significantly reduced in liver cancer cell lines compared with in a normal liver cell line. Demethylation of the HACE1 gene promoter increased HACE1 expression, inhibited the proliferation of liver cancer cells, and promoted OPTN ubiquitination and autophagy activity in liver cancer cells. In conclusion, activation of HACE1 expression by promoter demethylation may provide a suitable approach for anticancer therapy.

摘要

含HECT结构域和锚蛋白重复序列的E3泛素蛋白连接酶1(HACE1)在包括肝癌在内的多种癌症类型中经常下调或缺失。本研究的目的是检测HACE1基因的去甲基化是否能抑制肿瘤进展。在肝癌细胞系中检测了HACE1的表达。设计了针对HACE1基因启动子的成簇规律间隔短回文重复序列(CRISPR)-CRISPR相关蛋白(Cas)的去甲基化单向导RNA,并将其转染到肝癌细胞中。随后,通过MTT和集落形成试验检测细胞增殖,并通过免疫印迹法检测视黄醛结合蛋白(OPTN)的泛素化和微管相关蛋白1A/1B轻链3B蛋白水平。与正常肝细胞系相比,肝癌细胞系中HACE1的水平显著降低。HACE1基因启动子的去甲基化增加了HACE1的表达,抑制了肝癌细胞的增殖,并促进了肝癌细胞中OPTN的泛素化和自噬活性。总之,通过启动子去甲基化激活HACE1表达可能为抗癌治疗提供一种合适的方法。

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