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MicroRNA-122 confers sorafenib resistance to hepatocellular carcinoma cells by targeting IGF-1R to regulate RAS/RAF/ERK signaling pathways.
- Source :
-
Cancer Letters . Feb2016, Vol. 371 Issue 2, p171-181. 11p. - Publication Year :
- 2016
-
Abstract
- Sorafenib is the first-line treatment for advanced hepatocellular carcinoma (HCC), but the clinical response to sorafenib is seriously limited by drug resistance. In this study, we investigated the molecular mechanisms of sorafenib resistance in HCC cells. Our miRNA microarray data indicate that liver-specific miR-122 expression was significantly reduced in sorafenib-resistant cells. Overexpression of miR-122 made drug-tolerant cells sensitive to sorafenib and induced apoptosis. Insulin-like growth factor 1 receptor (IGF-1R) was validated as a target of miR-122 and was repressed by this miRNA. miR-122-induced apoptosis was repressed by the IGF-1R activator IGFI or IGFII. Conversely, the IGF-1R inhibitor PPP or NVP-AEW541 in combination with sorafenib significantly induced cell apoptosis and disrupted tolerance to drugs in vitro. These results indicated that activation of IGF-1R by ectopic down-regulation of miR-122 counteracted the effects of sorafenib-induced apoptosis, thus conferring sorafenib resistance. Further study revealed that activation of IGF-1R by miR-122 down-regulation contributed to activation of RAS/RAF/ERK signaling, which was associated with drug resistance. Our data imply that an intimate correlation between miR-122 and IGF-1R abnormal expression is a critical determinant of sorafenib tolerance. [ABSTRACT FROM AUTHOR]
- Subjects :
- *SORAFENIB
*LIVER cancer
*MICRORNA
*DRUG resistance
*SOMATOMEDIN C
*CELLULAR signal transduction
*GENETIC overexpression
*GENETICS
*PROTEIN metabolism
*RNA metabolism
*ANIMAL experimentation
*ANTINEOPLASTIC agents
*APOPTOSIS
*BINDING sites
*CELL lines
*CELL receptors
*DRUG resistance in cancer cells
*DOSE-effect relationship in pharmacology
*GENES
*GENETIC techniques
*HEPATOCELLULAR carcinoma
*LIVER tumors
*MICE
*RNA
*STEM cells
*TIME
*TRANSFERASES
*UREA
*VITAMIN B complex
*OLIGONUCLEOTIDE arrays
*GENE expression profiling
*PROTEIN kinase inhibitors
*PHARMACODYNAMICS
Subjects
Details
- Language :
- English
- ISSN :
- 03043835
- Volume :
- 371
- Issue :
- 2
- Database :
- Academic Search Index
- Journal :
- Cancer Letters
- Publication Type :
- Academic Journal
- Accession number :
- 112550376
- Full Text :
- https://doi.org/10.1016/j.canlet.2015.11.034