Combined effects of terazosin and genistein on a metastatic, hormone-independent human prostate cancer cell line.

Author: ChangKee-Lung, ChengHsiao-Ling, ChihTsai-Tung, HsiehBau-Shan, HuYu-Chen, HuangLi-Wen, ShyuHuey-Wen, SuShu-Jem

Paper Details 
Original Abstract of the Article :
Metastatic prostate cancer progresses from androgen-dependent to androgen-independent. Terazosin, a long-acting selective alpha1-adrenoreceptor antagonist, induces apoptosis of prostate cancer cells in an alpha1-adrenoreceptor-independent manner, while genistein, a major soy isoflavone, inhibits the...See full text at original site
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引用元:
https://doi.org/10.1016/j.canlet.2008.10.033

データ提供:米国国立医学図書館(NLM)

Combating Prostate Cancer: A Synergistic Approach

Prostate cancer, a common and often aggressive disease, requires a multi-pronged approach to effectively manage and treat. This study explores the potential of combining two promising agents, terazosin and genistein, to combat metastatic, hormone-independent prostate cancer.

A Powerful Combination for Prostate Cancer Treatment

The research demonstrates the synergistic effect of combining terazosin and genistein in inhibiting the growth of prostate cancer cells, particularly the aggressive DU-145 cell line. This combination was more effective in inducing apoptosis (programmed cell death) and reducing the expression of VEGF, a protein that promotes tumor growth, than either agent alone.

Hope for a More Effective Prostate Cancer Treatment

This study suggests that combining terazosin and genistein may offer a more potent and effective strategy for treating metastatic, hormone-independent prostate cancer. This approach could potentially improve treatment outcomes and enhance the quality of life for patients battling this challenging disease.

Dr. Camel's Conclusion

Just like a camel navigating a treacherous desert, finding effective treatments for prostate cancer requires a strategic approach. This research showcases the potential of combining terazosin and genistein, offering a promising avenue for overcoming the challenges associated with this disease.
Date :
  1. Date Completed 2009-03-18
  2. Date Revised 2018-12-01
Further Info :

Pubmed ID

19091461

DOI: Digital Object Identifier

10.1016/j.canlet.2008.10.033

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