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Bax and Bak are required for apoptosis induction by sulforaphane, a cruciferous vegetable-derived cancer chemopreventive agent.
- Source :
-
Cancer research [Cancer Res] 2005 Mar 01; Vol. 65 (5), pp. 2035-43. - Publication Year :
- 2005
-
Abstract
- Sulforaphane, a constituent of many edible cruciferous vegetables, including broccoli, effectively suppresses proliferation of cancer cells in culture and in vivo by causing apoptosis induction, but the sequence of events leading to cell death is poorly defined. Here, we show that multidomain proapoptotic Bcl-2 family members Bax and Bak play a critical role in apoptosis induction by sulforaphane. This conclusion is based on the following observations: (a) sulforaphane treatment caused a dose- and time-dependent increase in the protein levels of both Bax and Bak and conformational change and mitochondrial translocation of Bax in SV40-transformed mouse embryonic fibroblasts (MEF) derived from wild-type mice to trigger cytosolic release of apoptogenic molecules (cytochrome c and Smac/DIABLO), activation of caspase-9 and caspase-3, and ultimately cell death; (b) MEFs derived from Bax or Bak knockout mice resisted cell death by sulforaphane, and (c) MEFs derived from Bax and Bak double knockout mice exhibited even greater protection against sulforaphane-induced cytochrome c release, caspase activation, and apoptosis compared with wild-type or single knockout cells. Interestingly, sulforaphane treatment also caused a dose- and time-dependent increase in the protein level of Apaf-1 in wild-type, Bax-/-, and Bak-/- MEFs but not in double knockout, suggesting that Bax and Bak might regulate sulforaphane-mediated induction of Apaf-1 protein. A marked decline in the protein level of X-linked inhibitor of apoptosis on treatment with sulforaphane was also observed. Thus, it is reasonable to postulate that sulforaphane-induced apoptosis is amplified by a decrease in X-linked inhibitor of apoptosis level, which functions to block cell death by inhibiting activities of caspases. In conclusion, the results of the present study indicate that Bax and Bak proteins play a critical role in initiation of cell death by sulforaphane.
- Subjects :
- Animals
Apoptosis
Apoptosis Regulatory Proteins
Apoptotic Protease-Activating Factor 1
Carrier Proteins metabolism
Caspase 3
Caspase 9
Caspases metabolism
Cells, Cultured
Complement Membrane Attack Complex
Complement System Proteins
Cytochromes c metabolism
Enzyme Activation
Epithelial Cells
Fibroblasts drug effects
Fibroblasts metabolism
Glycoproteins metabolism
Isothiocyanates
Male
Mice
Mice, Knockout
Mitochondria drug effects
Mitochondrial Proteins metabolism
Prostate metabolism
Prostatic Neoplasms metabolism
Prostatic Neoplasms pathology
Protein Conformation drug effects
Protein Transport
Proteins metabolism
Sulfoxides
bcl-2 Homologous Antagonist-Killer Protein
bcl-2-Associated X Protein
Anticarcinogenic Agents pharmacology
Cell Proliferation drug effects
Chemoprevention
Membrane Proteins metabolism
Proto-Oncogene Proteins c-bcl-2 metabolism
Thiocyanates pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0008-5472
- Volume :
- 65
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Cancer research
- Publication Type :
- Academic Journal
- Accession number :
- 15753404
- Full Text :
- https://doi.org/10.1158/0008-5472.CAN-04-3616