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Cytotoxic activity of schisandrolic and isoschisandrolic acids involves induction of apoptosis

  • Ze Tian
  • , Lijia Xu
  • , Sibao Chen
  • , Liang Zhou
  • , Mengsu Yang
  • , Shilin Chen
  • , Peigen Xiao
  • , Erxi Wu

    Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

    Abstract

    Cycloartane triterpenoid schisandrolic acid and isoschisandrolic acid were isolated from Schisandra propinqua (Wall.) Baill (Schisandraceae). Their cytotoxicity was evaluated in several cancer cell lines and primary cultured normal mouse hepatocytes. The two triterpenoids showed moderate cytotoxic activity on all tested cell lines. Fluorescence staining and cell cycle analyses were employed to elucidate the primary mechanisms of their cytotoxicity. Our results showed that two triterpenoids exerted their cytotoxic activity via G0/G1 arrest and subsequent apoptosis. Furthermore, proteolytic cleavage of poly-ADP-ribose polymerase (PARP), substrate of the caspase family, was detected and associated with apoptosis in HepG2 cells induced by the two compounds. Copyright © 2007 S. Karger AG.
    Original languageEnglish
    Pages (from-to)257-262
    JournalChemotherapy
    Volume53
    Issue number4
    DOIs
    Publication statusPublished - Jul 2007

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Research Keywords

    • Apoptosis
    • Cell cycle
    • Isoschisandrolic acid
    • Poly-ADP-ribose polymerase
    • Schisandrolic acid

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