Paper Details 
Original Abstract of the Article :
Prostate cancer is the leading and most aggressive cancer around the world, several therapeutic approaches have emerged but none have achieved the satisfactory result. However, these therapeutic approaches face many challenges related to their delivery to target cells, including their in vivo decay,...See full text at original site
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引用元:
https://doi.org/10.1016/j.ejpb.2023.10.005

データ提供:米国国立医学図書館(NLM)

Nanomedicine Targets Survivin to Enhance Prostate Cancer Therapy

Prostate cancer is a major health concern worldwide, with limited treatment options. This study explores a novel approach using nanomedicine to deliver a combination of existing drugs, abiraterone and enzalutamide, directly to prostate cancer cells, targeting the survivin protein, a key player in cancer cell survival.

A Targeted Approach to Combatting Prostate Cancer

Researchers developed a nanomedicine system comprising abiraterone and enzalutamide encapsulated in survivin-targeted gold nanoparticles. This targeted delivery system demonstrated synergistic effects against prostate cancer cells, enhancing the potency of the drugs while minimizing side effects on healthy cells. The study also revealed the mechanism of action involving multiple signaling pathways in prostate cancer cells.

Hope on the Horizon for Prostate Cancer

This study offers a promising avenue for developing more effective and safer treatments for prostate cancer. The potential of nanomedicine to deliver drugs specifically to cancer cells while minimizing damage to healthy cells represents a significant advancement in cancer therapy.

Dr. Camel's Conclusion

This study is like a camel caravan equipped with advanced navigation technology, delivering a targeted and potent payload of abiraterone and enzalutamide directly to the heart of prostate cancer cells. The potential of this nanomedicine system is exciting, offering a glimmer of hope for a more effective and personalized approach to combating this challenging disease.

Date :
  1. Date Completed 2023-11-06
  2. Date Revised 2023-11-06
Further Info :

Pubmed ID

37797680

DOI: Digital Object Identifier

10.1016/j.ejpb.2023.10.005

Related Literature

SNS
PICO Info
in preparation
Languages

English

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