Abstract Title:

[10-gingerol inhibits proliferation of hepatocellular carcinoma HepG2 cells via Src/STAT3 signaling pathway].

Abstract Source:

Nan Fang Yi Ke Da Xue Xue Bao. 2018 Jul 30 ;38(8):1002-1007. PMID: 30187878

Abstract Author(s):

Jianxin Chen, Yifen Wu, Shuji Li, Hongyuan Wu, Libo Li

Article Affiliation:

Jianxin Chen


OBJECTIVE: To study the inhibitory effect of 10-gingerol on the proliferation of hepatocellular carcinoma HepG2 cells and the role of Src/STAT3 signaling pathway in mediating the effect.

METHODS: SYBYL-X2.1 software was used to simulate the interaction between 10-gingerol and Src. HepG2 cells treated with 10-gingerol at 1, 3, 10 orμol/L for 24 h were assessed for cell viability using MTT assay, and EdU staining was used to detect the cell proliferation and calculate the number of positive cells. The expressions of p-Src and p-STAT3 were detected using Western blotting, and the mRNA expressions of the target genes of STAT3 (cyclin D1 and CMCC) were detected using qPCR.

RESULTS: 10-gingerol was capable of forming hydrogen bond with such Src residues as TRY-340, MET-341, MET-314, ASP-404, and ILE-336. MTT assay showed that 10-gingerol at 3 and 10μmol/L significantly lowered the viability of HepG2 cells (<0.001). Treatment with 1, 3, and 10μmol/L 10-gingerol significantly reduces the number of EdU-positive HepG 2 cells (<0.001). Western blotting showed that 10-gingerol at 3 and 10μmol/L significantly decreased the phosphorylation levels of Src and STAT3 in HepG2 cells (<0.01). 10-gingerol at 1, 3, and 10μmol/L significantly decreased the mRNA expressions of cyclin D1 and CMCC as shown by qPCR (<0.01).

CONCLUSIONS: 10-gingerol can dose-dependently inhibit the proliferation of HepG2 cells and suppress the activation of Src and STAT3.

Study Type : In Vitro Study

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