The Renaissance of CDK Inhibitors in Breast Cancer Therapy: An Update on Clinical Trials and Therapy Resistance.

Author: AbdelmalakMary, AhmedMyra, AnwerMohammed, AshtonAnthony W, DuYanming, IvanchenkoPavel, JiaoXuanmao, PestellRichard, RandhawaAmritdeep, SinghRajanbir

Paper Details 
Original Abstract of the Article :
Cyclin-dependent kinases (CDKs) govern cell-cycle checkpoint transitions necessary for cancer cell proliferation. Recent developments have illustrated nuanced important differences between mono CDK inhibitor (CDKI) treatment and the combination therapies of breast cancers. The CDKIs that are current...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9655989/

データ提供:米国国立医学図書館(NLM)

CDK Inhibitors in Breast Cancer: A Renaissance of Hope

Breast cancer, a condition that affects millions of women worldwide, can feel like a vast desert landscape, where treatments and challenges can seem endless. This research delves into the world of cyclin-dependent kinase inhibitors (CDKIs), a class of drugs that show promise in combating breast cancer.

A New Era of CDKI Therapy

This research focuses on the use of CDKIs in breast cancer treatment, particularly those that target CDK4 and CDK6, which are involved in cell cycle regulation. It highlights the efficacy of these drugs, especially when combined with endocrine therapy.

Challenges and Opportunities

The research acknowledges the challenges associated with CDKI therapy, including resistance and side effects. It also points to the ongoing development of new therapies to enhance CDKI effectiveness and address the issue of drug resistance.

Dr.Camel's Conclusion

This research offers a promising glimpse into the future of breast cancer treatment, highlighting the renaissance of CDKI therapy. It underscores the importance of continued research to optimize these therapies, address resistance, and improve the overall treatment experience for breast cancer patients.

Date :
  1. Date Completed n.d.
  2. Date Revised 2022-11-17
Further Info :

Pubmed ID

36358806

DOI: Digital Object Identifier

PMC9655989

SNS
PICO Info
in preparation
Languages

English

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