Back to Search
Start Over
IFITM3 upregulates c-myc expression to promote hepatocellular carcinoma proliferation via the ERK1/2 signalling pathway
- Source :
- BioScience Trends. 13:523-529
- Publication Year :
- 2019
- Publisher :
- International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA), 2019.
-
Abstract
- Interferon-induced transmembrane protein 3 (IFITM3) is associated with cancer development. Proto-oncogene c-myc can promote tumor proliferation. However, collections of IFITM3 and c-myc in hepatocellular carcinoma (HCC) and the potential role and mechanisms of IFITM3 in c-myc-mediated tumor proliferation remain unclear. In this study, we investigated a positive correlation between the expression of IFITM3 and c-myc in HCC. The down-regulation of IFITM3 significantly reduced c-myc expression and inhibited the proliferation of HCC in vitro and in vivo. In addition, upregulated c-myc expression restored the decrease in cell proliferation caused by the downregulation of IFITM3, while downregulation of c-myc reduced the proliferation of HCC enhanced by IFITM3. Mechanistically, IFITM3 regulates c-myc expression via the ERK1/2 signalling pathway. In conclusion, a novel path of IFITM3-ERK1/2-c-myc regulatory circuitry was identified, and its dysfunction may lead to HCC tumorigenesis.
- Subjects :
- Health (social science)
General Medicine
Biology
medicine.disease_cause
medicine.disease
digestive system diseases
General Biochemistry, Genetics and Molecular Biology
Transmembrane protein
In vitro
Hedgehog signaling pathway
03 medical and health sciences
0302 clinical medicine
Downregulation and upregulation
In vivo
030220 oncology & carcinogenesis
Hepatocellular carcinoma
Cancer research
medicine
030211 gastroenterology & hepatology
Cancer development
Carcinogenesis
Subjects
Details
- ISSN :
- 18817823 and 18817815
- Volume :
- 13
- Database :
- OpenAIRE
- Journal :
- BioScience Trends
- Accession number :
- edsair.doi...........4478c69e2a515f645150b210902fef9d
- Full Text :
- https://doi.org/10.5582/bst.2019.01289