microRNAs: Key players in virus-associated hepatocellular carcinoma

(2019) microRNAs: Key players in virus-associated hepatocellular carcinoma. Journal of Cellular Physiology. pp. 12188-12225. ISSN 0021-9541

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Abstract

Hepatocellular carcinoma (HCC) is known as one of the major health problems worldwide. Pathological analysis indicated that a variety of risk factors including genetical (i.e., alteration of tumor suppressors and oncogenes) and environmental factors (i.e., viruses) are involved in beginning and development of HCC. The understanding of these risk factors could guide scientists and clinicians to design effective therapeutic options in HCC treatment. Various viruses such as hepatitis B virus (HBV) and hepatitis C virus (HCV) via targeting several cellular and molecular pathways involved in HCC pathogenesis. Among various cellular and molecular targets, microRNAs (miRNAs) have appeared as key players in HCC progression. miRNAs are short noncoding RNAs which could play important roles as oncogenes or tumor suppressors in several malignancies such as HCC. Deregulation of many miRNAs (i.e., miR-222, miR-25, miR-92a, miR-1, let-7f, and miR-21) could be associated with different stages of HCC. Besides miRNAs, exosomes are other particles which are involved in HCC pathogenesis via targeting different cargos, such as DNAs, RNAs, miRNAs, and proteins. In this review, we summarize the current knowledge of the role of miRNAs and exosomes as important players in HCC pathogenesis. Moreover, we highlighted HCV- and HBV-related miRNAs which led to HCC progression.

Item Type: Article
Keywords: exosome hbv hcv hepatocellular carcinoma microrna therapy hepatitis-b-virus epithelial-mesenchymal transition suppresses cell-proliferation increases drug-resistance regulates g(1)/s transition aberrant DNA methylation induced up-regulation targeting c-myc growth-factor-c nf-kappa-b
Divisions: Faculty of Medicine > Departments of Clinical Sciences > Department of Infectious Diseases
Page Range: pp. 12188-12225
Journal or Publication Title: Journal of Cellular Physiology
Journal Index: ISI
Volume: 234
Number: 8
Identification Number: https://doi.org/10.1002/jcp.27956
ISSN: 0021-9541
Depositing User: Zahra Otroj
URI: http://eprints.mui.ac.ir/id/eprint/9941

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