4.4 Article

Progress of HDAC Inhibitor Panobinostat in the Treatment of Cancer

期刊

CURRENT DRUG TARGETS
卷 15, 期 6, 页码 622-634

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1389450115666140306152642

关键词

Combined therapy; hematologic malignancies; histone deacetylase inhibitors; monotherapy; panobinostat; solid tumors

资金

  1. National Scientific and Technological Major Project of Ministry of Science and Technology of China [2011ZX09401-015]
  2. National Natural Science Foundation of China [21302111, 21172134]
  3. China Postdoctoral Science Foundation [2013M540558]
  4. Postdoctoral Innovation Project Foundation of Shandong Province [201303090]
  5. Independent Innovation Foundation of Shandong University, IIFSDU [2013GN013]
  6. National Cancer Institute of the National Institute of Health [R01CA163452]
  7. National High-tech R&D Program of China, 863 Program [2014AA020523]

向作者/读者索取更多资源

Histone deacetylases are a class of enzymes that play important roles in post translational modifications of histones by deacetylating the lysine residues as well as interacting with various non-histone proteins. This type of enzymes is closely related to oncogenesis and has been proved to be attractive targets for designing novel anti-cancer agents. Over the last 10 years, a large number of HDACs have entered pre-clinical and/or clinical trials. Among these drug candidates, the pan-HDAC inhibitor, panobinostat demonstrated high therapeutic potential as monotherapy and combined therapy in both preclinical models and clinical cancer patients. In this review, we have mainly focused on the recent progress of the clinical studies about panobinostat, and discussed its anti-cancer effects and molecular rationale for the treatment strategies.

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