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microRNA-19a-3p promotes tumor metastasis and chemoresistance through the PTEN/Akt pathway in hepatocellular carcinoma.
- Source :
-
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie [Biomed Pharmacother] 2018 Sep; Vol. 105, pp. 1147-1154. Date of Electronic Publication: 2018 Jun 21. - Publication Year :
- 2018
-
Abstract
- microRNA-19a-3p (miR-19a-3p) has been reported to regulate cell proliferation in hepatocellular carcinoma (HCC), but its role in HCC metastasis remains unknown. In this study, miR-19a-3p was noted to be upregulated in HCC specimens and cell lines. Aberrant expression of miR-19a-3p stimulated HCC cell metastasis, and phosphatase and tensin homolog (PTEN) was shown to be a direct target of miR-19a-3p. miR-19a-3p-mediated HCC metastasis was reversed by restoration of PTEN or could be imitated by silencing of PTEN. Modulation of miR-19a-3p also altered expression of phosphorylated Akt, a downstream mediator of PTEN. Moreover, aberrant expression of miR-19a-3p induced sorafenib resistance by regulating the PTEN/Akt pathway. In conclusion, ectopic expression of miR-19a-3p contributes to HCC metastasis and chemoresistance by modulating PTEN expression and the PTEN-dependent pathways.<br /> (Copyright © 2018 Elsevier Masson SAS. All rights reserved.)
- Subjects :
- Carcinoma, Hepatocellular genetics
Carcinoma, Hepatocellular pathology
Cell Line, Tumor
Gene Expression Regulation, Neoplastic
Hepatocytes metabolism
Hepatocytes pathology
Humans
Liver Neoplasms genetics
Liver Neoplasms pathology
MicroRNAs genetics
Signal Transduction physiology
Carcinoma, Hepatocellular metabolism
Drug Resistance, Neoplasm physiology
Liver Neoplasms metabolism
MicroRNAs biosynthesis
PTEN Phosphohydrolase metabolism
Proto-Oncogene Proteins c-akt metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1950-6007
- Volume :
- 105
- Database :
- MEDLINE
- Journal :
- Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
- Publication Type :
- Academic Journal
- Accession number :
- 30021351
- Full Text :
- https://doi.org/10.1016/j.biopha.2018.06.097