Epi-Drugs and Epi-miRs: Moving Beyond Current Cancer Therapies

(2016) Epi-Drugs and Epi-miRs: Moving Beyond Current Cancer Therapies. Current Cancer Drug Targets. pp. 773-788. ISSN 1568-0096

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Abstract

Epigenetic modifications determine phenotypic characteristics in a reversible, stable and genotype-independent manner. Epigenetic modifications mainly encompass CpG island methylation and histone modifications, both being important in the pathogenesis of malignancies. The reversibility of epigenetic phenomenon provides a suitable therapeutic option that is reactivation of epigenetically silenced tumor-suppressor genes. Inhibition of DNA methyltransferase, histone deacetylase and Aurora B kinase, individually or collectively, could feasibly prevent or reverse the impact of epigenetic silencing. MicroRNAs miRNAs are an important layer of epigenetic controlling of gene expression, and serve as diagnostic and prognostic biomarkers as well as treatment targets for several types of cancer. miRNAs are involved inepigenetically silencing or activation of genes, tumor-suppressor genes and oncogenes, and their modulation opens new horizons for designing novel cancer therapeutic agents.

Item Type: Article
Keywords: cancer epigenetics DNA methyltransferase inhibitor epi-drugs epi-mirs histone deacetylase inhibitor histone deacetylase inhibitor advanced solid tumors chronic myelogenous leukemia cpg island hypermethylation human colorectal-cancer acute myeloid-leukemia cell-cycle kinases phase-ii trial DNA methylation prostate-cancer
Page Range: pp. 773-788
Journal or Publication Title: Current Cancer Drug Targets
Journal Index: ISI
Volume: 16
Number: 9
Identification Number: https://doi.org/10.2174/1568009616666151207110143
ISSN: 1568-0096
Depositing User: مهندس مهدی شریفی
URI: http://eprints.mui.ac.ir/id/eprint/2997

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