1. Academic Validation
  2. Monomer gypenoside LI from Gynostemma pentaphyllum inhibits cell proliferation and upregulates expression of miR-128-3p in melanoma cells

Monomer gypenoside LI from Gynostemma pentaphyllum inhibits cell proliferation and upregulates expression of miR-128-3p in melanoma cells

  • J Biochem Mol Toxicol. 2020 May;34(5):e22460. doi: 10.1002/jbt.22460.
Ma-Li Zu 1 2 Xiang-Lan Piao 2 Jia-Mei Gao 1 Shao-Fang Xing 2 Lin-Hua Liu 1
Affiliations

Affiliations

  • 1 Department of Biochemistry, College of Basic Medical Sciences, Dalian Medical University, Dalian, Liaoning, China.
  • 2 School of Pharmacy, Minzu University of China, Beijing, China.
Abstract

Gypenosides have Anticancer activity against many cancers. Gypenoside LI is a gypenoside monomer from Gynostemma pentaphyllum, its pharmacological functions in melanoma have not been reported. In this study, we found that gypenoside LI had a potent cytotoxic effect on melanoma cells. Gypenoside LI can induce intrinsic Apoptosis along with S phase arrest. Furthermore, gypenoside LI inhibited the colony formation ability of melanoma through inhibition of the Wnt/β-catenin signaling pathway. Interestingly, we also found that gypenoside LI can induce the upregulation of the tumor suppressor miR-128-3p during melanoma Apoptosis. In contrast, gypenoside LI induced Apoptosis, cell cycle arrest, and inhibition of the Wnt/β-catenin signaling pathway, which were abolished by overexpression of the miR-128-3p inhibitor in A375 cells. Taken together, these results showed that gypenoside LI could inhibit human melanoma cells through inducing Apoptosis, arresting cell cycle at the S phase and suppressing the Wnt/β-catenin signaling pathway in a miR-128-3p dependent manner.

Keywords

Wnt/β-catenin signaling pathway; apoptosis; gypenoside LI; melanoma; miR-128-3p.

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