HCV core protein promotes hepatocyte proliferation and chemoresistance by inhibiting NR4A1
Creators
Description
This study investigated the effect of HCV core protein on the proliferation of hepatocytes and hepatocellular carcinoma cells (HCC), the influence of HCV core protein on HCC apoptosis induced by the chemotherapeutic agent cisplatin, and the mechanism through which HCV core protein acts as a potential oncoprotein in HCV-related HCC by measuring the levels of NR4A1 and Runt-related transcription factor 3 (RUNX3), which are associated with tumor suppression and chemotherapy resistance. In the present study, PcDNA3.1-core and RUNX3 siRNA were transfected into LO2 and HepG2 cells using Lipofectamine 2000. LO2-core, HepG2-core, LO2-RUNX3 low and control cells were treated with different concentrations of cisplatin for 72 h, and cell proliferation and apoptosis were assayed using the CellTiter 96®Aqueous Non-Radioactive Cell Proliferation Assay Kit. Western blot and real time PCR analyses were used to detect NR4A1, RUNX3, smad7, Cyclin D1 and BAX. Confocal microscopy was used to determine the levels of NR4A1 in HepG2 and HepG2-core cells. The growth rate of HepG2-core cells was considerably greater than that of HepG2 cells. HCV core protein increased the expression of cyclin D1 and decreased the expressions of NR4A1 and RUNX3. In LO2 – RUNX3 low, the rate of cell proliferation and the level of cisplatin resistance were the same as in the LO2 -core. These results suggest that HCV core protein decreases the sensitivity of hepatocytes to cisplatin by inhibiting the expression of NR4A1 and promoting the expression of smad7, which negatively regulates the TGF-β pathway. This effect results in down regulation of RUNX3, a target of the TGF-β pathway. Taken together, these findings indicate that in hepatocytes, HCV core protein increases drug resistance and inhibits cell apoptosis by inhibiting the expressions of NR4A1 and RUNX3. - Highlights: • HCV core protein inhibits HepG2 cell sensitivity to cisplatin. • Core expression in HepG2 decreases expression of NR4A1. • Core protein increases the expression of smad7 in hepatocytes. • Core protein inhibits HepG2 cells apoptosis induced by cisplatin.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2015.09.091Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2015.09.091;
- PII
- S0006-291X(15)30608-2;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 466
- Journal Issue
- 3
- Journal Page Range
- p. 592-598
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48037332
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- APOPTOSIS; CELL PROLIFERATION; CHEMOTHERAPY; CONCENTRATION RATIO; HEPATOMAS; LIVER CELLS; ONCOGENES; POLYMERASE CHAIN REACTION; SENSITIVITY; TRANSCRIPTION FACTORS
- Descriptors DEC
- ANIMAL CELLS; CARCINOMAS; DIMENSIONLESS NUMBERS; DISEASES; GENE AMPLIFICATION; GENES; MEDICINE; NEOPLASMS; ORGANIC COMPOUNDS; PROTEINS; SOMATIC CELLS; THERAPY
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.