| Literature DB >> 27582311 |
Muhammed H Rahaman, Malika Kumarasiri, Laychiluh B Mekonnen1, Mingfeng Yu1, Sarah Diab1, Hugo Albrecht1, Robert W Milne1, Shudong Wang2.
Abstract
Cyclin-dependent kinase 9 (CDK9) is a key transcriptional regulator and a lucrative target for cancer treatment. Targeting CDK9 can effectively confine the hyperactivity of androgen receptor and the constitutive expression of anti-apoptotic proteins; both being main causes of prostate cancer (PCa) development and progression. In castrate-resistant PCa, traditional therapies that only target androgen receptor (AR) have become obsolete due to reprograming in AR activity to make the cells independent of androgen. CDK9 inhibitors may provide a new and better therapeutic opportunity over traditional treatment options by targeting both androgen receptor activity and anti-apoptotic proteins, improving the chances of positive outcomes, especially in patients with the advanced disease. This review focuses on biological functions of CDK9, its involvement with AR and the potential for therapeutic opportunities in PCa treatment.Entities:
Keywords: CDK9; RNAPII transcription; anti-apoptotic proteins; apoptosis; prostate cancer; therapeutics
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Year: 2016 PMID: 27582311 DOI: 10.1530/ERC-16-0299
Source DB: PubMed Journal: Endocr Relat Cancer ISSN: 1351-0088 Impact factor: 5.678