Critical role of pro-apoptotic Bcl-2 family members in andrographolide-induced apoptosis in human cancer cells

Biochem Pharmacol. 2006 Jul 14;72(2):132-44. doi: 10.1016/j.bcp.2006.04.019. Epub 2006 Apr 29.

Abstract

Andrographolide (Andro), a diterpenoid lactone isolated from a traditional herbal medicine Andrographis paniculata, is known to possess potent anti-inflammatory activity. In this study, Andro induced apoptosis in human cancer cells via activation of caspase 8 in the extrinsic death receptor pathway and subsequently with the participation of mitochondria. Andro triggered a caspase 8-dependent Bid cleavage, followed by a series of sequential events including Bax conformational change and mitochondrial translocation, cytochrome c release from mitochondria, and activation of caspase 9 and 3. Inhibition of caspase 8 blocked Bid cleavage and Bax conformational change. Consistently, knockdown of Bid protein using small interfering RNA (siRNA) technique suppressed Andro-induced Bax conformational change and apoptosis. In conclusion, the pro-apoptotic Bcl-2 family members (Bid and Bax) are the key mediators in relaying the cell death signaling initiated by Andro from caspase 8 to mitochondria and then to downstream effector caspases, and eventually leading to apoptotic cell death.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Apoptosis / physiology
  • Caspases / metabolism
  • Cell Line, Tumor
  • Cytochromes c / metabolism
  • Diterpenes / pharmacology*
  • Humans
  • Protein Conformation
  • Protein Transport
  • Proto-Oncogene Proteins c-bcl-2 / physiology*
  • RNA, Small Interfering
  • Tumor Cells, Cultured

Substances

  • Diterpenes
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Small Interfering
  • andrographolide
  • Cytochromes c
  • Caspases