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Resveratrol induces p53-independent, X-linked inhibitor of apoptosis protein (XIAP)-mediated Bax protein oligomerization on mitochondria to initiate cytochrome c release and caspase activation.

Resveratrol, a naturally occurring phytoalexin, is known to induce apoptosis in multiple cancer cell types, but the underlying molecular mechanisms remain unclear. Here, we show that resveratrol induced p53-independent, X-linked inhibitor of apoptosis protein (XIAP)-mediated translocation of Bax to mitochondria where it underwent oligomerization to initiate apoptosis. Resveratrol treatment promoted interaction between Bax and XIAP in the cytosol and on mitochondria, suggesting that XIAP plays a critical role in the activation and translocation of Bax to mitochondria. This process did not involve p53 but required accumulation of Bim and t-Bid on mitochondria. Bax primarily underwent homo-oligomerization on mitochondria and played a major role in release of cytochrome c to the cytosol. Bak, another key protein that regulates the mitochondrial membrane permeabilization, did not interact with p53 but continued to associate with Bcl-xL. Thus, the proapoptotic function of Bak remained suppressed during resveratrol-induced apoptosis. Caspase-9 silencing inhibited resveratrol-induced caspase activation, whereas caspase-8 knockdown did not affect caspase activity, suggesting that resveratrol induces caspase-9-dependent apoptosis. Together, our findings characterize the molecular mechanisms of resveratrol-induced caspase activation and subsequent apoptosis in cancer cells.

Pubmed ID: 21712378


  • Gogada R
  • Prabhu V
  • Amadori M
  • Scott R
  • Hashmi S
  • Chandra D


The Journal of biological chemistry

Publication Data

August 19, 2011

Associated Grants

  • Agency: NCI NIH HHS, Id: CA016056
  • Agency: NCI NIH HHS, Id: K01 CA123142

Mesh Terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal
  • Apoptosis
  • Caspase 8
  • Caspase 9
  • Cytochromes c
  • Enzyme Activation
  • Humans
  • Jurkat Cells
  • Mice
  • Mice, Knockout
  • Mitochondria
  • Protein Multimerization
  • Stilbenes
  • Tumor Suppressor Protein p53
  • X-Linked Inhibitor of Apoptosis Protein
  • bcl-2-Associated X Protein