Skip to main navigation Skip to search Skip to main content

Taiwanin A induced cell cycle arrest and p53-dependent apoptosis in human hepatocellular carcinoma HepG2 cells

  • Pai Jiun Ho
  • , Chen Kung Chou
  • , Yueh Hsiung Kuo
  • , Lan Chun Tu
  • , Sheau Farn Yeh*
  • *Corresponding author for this work
  • National Yang Ming Chiao Tung University
  • National Taiwan University

Research output: Contribution to journalJournal Article peer-review

33 Scopus citations

Abstract

Taiwanin A, a lignan isolated from Taiwania cryptomerioides Hayata, has previously been reported to have cytotoxicity against human tumor cells, but the mechanisms are unclear. In this study, we examined the molecular mechanism of cell death of human hepatocellular carcinoma HepG2 cells induced by Taiwanin A. Taiwanin A has been found to induce cell cycle arrest at G2/M phase as well as caspase-3-dependent apoptosis within 24 h. We performed both in vitro turbidity assay and immunofluorescence staining of tubulin to show that Taiwanin A can inhibit microtubule assembly. Moreover, the tumor suppressor protein p53 in HepG2 cells was activated by Taiwanin A within 12 h. Inhibition of p53 by either pifithrin-α or by short hairpin RNA which blocks p53 expression attenuates Taiwanin A cytotoxicity. Our results demonstrate that Taiwanin A can act as a new class of microtubule damaging agent, arresting cell cycle progression at mitotic phase and inducing apoptosis through the activation of p53.

Original languageEnglish
Pages (from-to)493-503
Number of pages11
JournalLife Sciences
Volume80
Issue number5
DOIs
StatePublished - 09 01 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

Keywords

  • Apoptosis
  • Cell cycle arrest
  • Microtubule disruption
  • Taiwanin A
  • p53

Fingerprint

Dive into the research topics of 'Taiwanin A induced cell cycle arrest and p53-dependent apoptosis in human hepatocellular carcinoma HepG2 cells'. Together they form a unique fingerprint.

Cite this