7,7′′-Dimethoxyagastisflavone-induced apoptotic or autophagic cell death in different cancer cells

Chia Hsiang Hwang, Yu Ling Lin, Yen Ku Liu, Chia Hung Chen, Hsin Yi Wu, Cheng Chang Chang, Chao Yuan Chang, Yu Kuo Chang, Yi Han Chiu, Kuang-Wen Liao*, Yiu Kay Lai

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

7,7′′-Dimethoxyagastisflavone (DMGF), a biflavonoid isolated from the needles of Taxus × media cv. Hicksii, was evaluated for its antiproliferative and antineoplastic effects in three human cancer cell lines. Interestingly, DMGF caused cell death via different pathways in different cancer cells. DMGF induced apoptosis, activated caspase-3 activity and changed the mitochondrial membrane potential in HT-29 human colon cancer cells. However, the apoptotic pathway is not the major pathway involved in DMGF-induced cell death in A549 human lung cancer cells and HepG2 human hepatoma cells. Treatment with 3-MA, an inhibitor of autophagy, significantly decreased DMGF-induced cell death in HepG2 and A549 cells, but did not affect DMGF-induced cell death in HT-29 cells. Following DMGF treatment, the HepG2 cells increased expression of LC3B-II, a marker used to monitor autophagy in cells. Thus, DMGF induced apoptotic cell death in HT-29 cells, triggered both apoptotic and autophagic death in A549 cells and induced autophagic cell death in HepG2 cells.

Original languageEnglish
Pages (from-to)528-534
Number of pages7
JournalPhytotherapy Research
Volume26
Issue number4
DOIs
StatePublished - 1 Apr 2012

Keywords

  • 7,7′′-dimethoxyagastisflavone
  • apoptosis
  • autophagy
  • biflavonoid
  • Taxus × media cv. Hicksii

Fingerprint Dive into the research topics of '7,7′′-Dimethoxyagastisflavone-induced apoptotic or autophagic cell death in different cancer cells'. Together they form a unique fingerprint.

Cite this