Targeting miRNAs by histone deacetylase inhibitors (HDACi): Rationalizing epigenetics-based therapies for breast cancer

被引:27
作者
Ediriweera, Meran Keshawa [1 ]
Cho, Somi Kim [1 ,2 ,3 ]
机构
[1] Jeju Natl Univ, Subtrop Trop Organism Gene Bank, Jeju 63243, South Korea
[2] Jeju Natl Univ, Coll Appl Life Sci, Fac Biotechnol, SARI, Jeju 63243, South Korea
[3] Jeju Natl Univ, Interdisciplinary Grad Program Adv Convergence Te, Jeju 63243, South Korea
基金
新加坡国家研究基金会;
关键词
miRNA; Histone deacetylase inhibitors; Breast cancer; Epigenetics; MICRORNA EXPRESSION PROFILES; ESTROGEN-RECEPTOR-ALPHA; GENE-EXPRESSION; E-CADHERIN; INDUCE APOPTOSIS; TUMOR INVASION; MIR-200; FAMILY; MESSENGER-RNA; CELLS; METASTASIS;
D O I
10.1016/j.pharmthera.2019.107437
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MicroRNAs (miRNAs) belong to a group of short RNA molecules of similar to 22 nucleotides that play a significant role in the regulation of gene expression through post-transcriptional regulatory mechanisms They can directly interact with their target mRNA molecules and induce target gene silencing. Many investigations over the past decade have revealed the involvement of different miRNAs in essential biological events. The expression of a considerable number of miRNAs is tightly regulated through epigenetic events such as histone modifications and DNA methylation. Notably, irregularities in these epigenetic events are associated with aberrant expression of miRNAs in a range of diseases including cancer. Impaired epigenetic events associated with aberrant expression of miRNAs can be pharmacologically modified using chromatin modifying drugs. Numerous pre-clinical and clinical data demonstrate that histone deacetylase inhibitors (HDACi) can re-establish the expression of aberrantly expressed miRNAs in a range of cancer types, rationalizing miRNAs as potential drug targets. This review highlights evidence from investigations assessing the effects of different classes of HDACi on miRNA expression in breast cancer (BC). (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页数:15
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