AI Article Synopsis

  • A novel dammarane triterpenoid saponin, Cypaliuruside F, was isolated from leaves and examined for its antitumor effects on HepG2 liver cancer cells using various assays like MTT and flow cytometry.
  • The study involved network pharmacology and molecular docking to identify key targets of Cypaliuruside F in fighting hepatocellular carcinoma (HCC).
  • Results showed that Cypaliuruside F hinders HepG2 cell growth by triggering apoptosis and cell cycle arrest, primarily by downregulating mTOR, STAT3, and Bcl-2 while enhancing Bax expression.

Article Abstract

An undescribed dammarane triterpenoid saponin Cypaliuruside F was isolated from the leaves of in our preliminary study. The MTT assay, flow cytometry, cell scratch, and DAPI staining were used to detect the antitumor effects of Cypaliuruside F on HepG2 cells. Subsequently, network pharmacology and molecular docking analysis were used to analyse the key targets of Cypaliuruside F against HCC. In addition, a Western blot was performed to determine the effects of Cypaliuruside F on the expression of key proteins in HepG2 cells. The experimental results indicated that the damarane triterpenoid saponin Cypaliuruside F from inhibits the proliferation of HepG2 cells by inducing apoptosis and cell cycle arrest. These changes may promote the apoptosis of HepG2 cells by inhibiting the expression of mTOR, STAT3, and Bcl-2 while activating Bax.

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Source
http://dx.doi.org/10.1080/14786419.2024.2355590DOI Listing

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