| Literature DB >> 31852866 |
Jiaqi Min1,2, Junwen Hu1,3, Chen Luo1, Jinfeng Zhu1, Jiefeng Zhao1, Zhengming Zhu1, Linquan Wu1, Rongfa Yuan1.
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.Entities:
Keywords: ERK1/2 signalling pathway; IFITM3; c-myc; hepatocellular carcinoma; proliferation
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Year: 2019 PMID: 31852866 DOI: 10.5582/bst.2019.01289
Source DB: PubMed Journal: Biosci Trends ISSN: 1881-7815 Impact factor: 2.400