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Research ArticleExperimental Studies

Molecular Mechanisms of (-)-Gossypol-induced Apoptosis in Human Prostate Cancer Cells

YI-WEN HUANG, LI-SHU WANG, HSIANG-LIN CHANG, WEIPING YE, MICHAEL K. DOWD, PETER J. WAN and YOUNG C. LIN
Anticancer Research May 2006, 26 (3A) 1925-1933;
YI-WEN HUANG
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LI-SHU WANG
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HSIANG-LIN CHANG
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WEIPING YE
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MICHAEL K. DOWD
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PETER J. WAN
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YOUNG C. LIN
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  • For correspondence: lin.15{at}osu.edu
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Abstract

Background: Gossypol, a natural compound present in cottonseeds, displays antiproliferative and pro-apoptotic effects against various cancer cells. The (-)-gossypol enantiomer is a more potent inhibitor of cancer cell growth. Here, the molecular mechanisms of apoptosis induced by (-)-gossypol were studied in human prostate cancer cells. Materials and Methods: After the prostate cancer cell DU-145 had been treated with (-)-gossypol, the trypan blue exclusion assay and DNA fragment end-labeling assay were used to stain the dead cells and to detect DNA laddering, respectively. The effects of (-)-gossypol on the expression of apoptotic-regulated gene markers in both death receptor- and mitochondria-mediated apoptotic pathways, such as the Bcl-2 family and caspase, etc., were detected by RT-PCR and Western blot analysis. To further investigate the apoptotic pathways induced by (-)-gossypol, different caspase inhibitors were used to block caspase activities and cell viability was detected by the CellTiter 96ì AQueous assay in DU-145 cells. Results: At a 5-10 μM dose-level, (-)-gossypol significantly enhanced apoptosis measured by DNA fragmentation. (-)-Gossypol caused apoptosis in DU-145 cells through the down-regulation of Bcl-2 and Bcl-xL and the up-regulation of Bax at the mRNA and protein levels. (-)-Gossypol also activated caspases-3, -8 and -9 and increased PARP [poly (ADP-ribose) polymerase] cleavage. Furthermore, (-)-gossypol-induced apoptosis might be due to an increase in CAD (caspase-activated deoxyribonuclease) proteins and a decrease in ICAD (inhibitor of CAD) proteins. By using caspase inhibitors, (-)-gossypol caused apoptosis via the caspase-dependent pathways. Conclusion: Our results indicated that the apoptotic processes caused by (-)-gossypol are mediated by the regulation of the Bcl-2 and caspase families in human prostate cancer cells. Our data also suggested that (-)-gossypol may have chemotheraputic benefits for prostate cancer patients.

  • (-)-Gossypol
  • apoptosis
  • Bcl-2
  • caspase
  • prostate cancer cell

Footnotes

  • Received February 27, 2006.
  • Accepted March 28, 2006.
  • Copyright© 2006 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved
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May-June 2006
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Molecular Mechanisms of (-)-Gossypol-induced Apoptosis in Human Prostate Cancer Cells
YI-WEN HUANG, LI-SHU WANG, HSIANG-LIN CHANG, WEIPING YE, MICHAEL K. DOWD, PETER J. WAN, YOUNG C. LIN
Anticancer Research May 2006, 26 (3A) 1925-1933;

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Molecular Mechanisms of (-)-Gossypol-induced Apoptosis in Human Prostate Cancer Cells
YI-WEN HUANG, LI-SHU WANG, HSIANG-LIN CHANG, WEIPING YE, MICHAEL K. DOWD, PETER J. WAN, YOUNG C. LIN
Anticancer Research May 2006, 26 (3A) 1925-1933;
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