Histone Deacetylases and Their Regulatory MicroRNAs in Hepatocarcinogenesis

被引:25
|
作者
Kim, Hyung Seok [1 ,2 ]
Shen, Qingyu [1 ,2 ]
Nam, Suk Woo [1 ,2 ,3 ]
机构
[1] Catholic Univ Korea, Coll Med, Dept Pathol, Seoul 06591, South Korea
[2] Catholic Univ Korea, Funct RNom Res Ctr, Seoul 06591, South Korea
[3] Catholic Univ Korea, Canc Evolut Res Ctr, Seoul 06591, South Korea
基金
新加坡国家研究基金会;
关键词
Histone Deacetylases; MicroRNAs; Carcinoma; Hepatocellular; HUMAN HEPATOCELLULAR-CARCINOMA; TUMOR-SUPPRESSOR; CELL-CYCLE; MESENCHYMAL TRANSITION; MALIGNANT PROGRESSION; EXPRESSION; APOPTOSIS; OVEREXPRESSION; CANCER; GENE;
D O I
10.3346/jkms.2015.30.10.1375
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A growing body of evidence suggests that epigenetic modifications are promising potential mechanisms in cancer research. Among the molecules that mediate epigenetic mechanisms, histone deacetylases (HDACs) are critical regulators of gene expression that promote formation of heterochromatin by deacetylating histone and non-histone proteins. Aberrant regulation of HDACs contributes to malignant transformation and progression in a wide variety of human cancers, including hepatocellular carcinoma (HCC), gastric cancer, lung cancer, and other cancers. Thus, the roles of HDACs have been extensively studied because of their potential as therapeutic targets. However, the underlying mechanism leading to deregulation of individual HDACs remains largely unknown. Some reports have suggested that functional microRNAs (miRNAs) modulate epigenetic effector molecules including HDACs. Here, we describe the oncogenic or tumor suppressive functions of HDAC families and their regulatory miRNAs governing HDAC expression in hepatocarcinogenesis.
引用
收藏
页码:1375 / 1380
页数:6
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