Effects of microtubule inhibitors-taxol, vinblastine and estramustine on the growth and p53 gene expression in the hormone independent human prostatic JCA-1 cells.

Author: AnS, DarbyE, HsiehT C, MallouhC, NgC, WuJ M

Paper Details 
Original Abstract of the Article :
Treatment of the JCA-1 prostate cells with different concentrations of microtubule inhibitors-taxol (paclitaxel) vinblastine, and estramustine-was accompanied by reduced cell growth and, correspondingly, characteristic morphological changes. The reduction of cellular proliferation was unlikely to be...See full text at original site
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引用元:
https://pubmed.ncbi.nlm.nih.gov/9042236

データ提供:米国国立医学図書館(NLM)

Microtubule Inhibitors for Prostate Cancer: A Promising New Direction

The fight against prostate cancer, like a desert battle, requires a multi-pronged approach. This study investigates the effects of microtubule inhibitors, such as taxol (paclitaxel), vinblastine, and estramustine, on the growth and p53 gene expression of hormone-independent human prostatic JCA-1 cells.

Microtubule Inhibitors' Potential for Prostate Cancer Treatment

The study found that microtubule inhibitors effectively reduced cell growth in JCA-1 cells, suggesting their potential as complementary treatment modalities for patients with hormonally independent prostate cancer.

New Strategies for Fighting Prostate Cancer

The discovery of microtubule inhibitors' efficacy against hormone-independent prostate cancer provides new hope for patients seeking effective treatments. It's like finding a new oasis in a seemingly barren desert, offering a source of hope and potential relief.

Dr.Camel's Conclusion

This study highlights the potential of microtubule inhibitors as a promising new approach for treating hormone-independent prostate cancer. Further research is needed to optimize their use and explore their potential in combination therapies, but microtubule inhibitors offer a potentially valuable tool in the fight against this challenging disease.

Date :
  1. Date Completed 1997-03-27
  2. Date Revised 2015-11-19
Further Info :

Pubmed ID

9042236

DOI: Digital Object Identifier

9042236

Related Literature

SNS
PICO Info
in preparation
Languages

English

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