HDAC inhibitors with potential to overcome drug resistance in castration-resistant prostate cancer

被引:27
作者
Biersack, Bernhard [1 ]
Nitzsche, Bianca [2 ]
Hoepfner, Michael [2 ]
机构
[1] Univ Bayreuth, Organ Chem Lab, Univ Str 30, D-95440 Bayreuth, Germany
[2] Charite Univ Med Berlin, Inst Physiol, D-10117 Berlin, Germany
关键词
Histone deacetylases; HDAC inhibitors; castration-resistant prostate cancer; drug resistance; HISTONE DEACETYLASE INHIBITORS; GROWTH-FACTOR RECEPTOR; ANDROGEN RECEPTOR; HORMONAL-THERAPY; PHASE-II; CELLS; ENZALUTAMIDE; COMBINATION; EXPRESSION; CUDC-101;
D O I
10.20517/cdr.2021.105
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epigenetic mechanisms play an important role in the development and persistence of cancer, and histone deacetylase (HDAC) inhibitors are promising anticancer drugs targeting epigenetic modes. Efficient anticancer drugs for the treatment of castration-resistant prostate cancer (CRPC) are sought, and approved HDAC inhibitors have shown promising results on the one hand and severe drawbacks on the other hand. Hence, ways to break the drug resistance mechanisms of existing HDAC inhibitors as well as the design of new promising HDAC inhibitors which can overcome the disadvantages of the classic HDAC inhibitors are of great importance. In this work, HDAC inhibitors with the potential to become a mainstay for the treatment of CRPC in the future as well as suitable combination treatments of HDAC inhibitors with other anticancer drugs leading to considerable synergistic effects in treated CRPCs are discussed.
引用
收藏
页码:64 / 79
页数:16
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