Advances and Challenges of HDAC Inhibitors in Cancer Therapeutics

• Published in: Advances in cancer research Vol. 138; p. 183
• Main Authors: McClure, Jesse J, Li, Xiaoyang, Chou, C James
• Format: Journal Article
• Language: English
• Published: United States 2018
• Subjects: Animals; Histone Deacetylase Inhibitors - therapeutic use; Histone Deacetylases - chemistry; Humans; Neoplasms - drug therapy; Neoplasms - enzymology; Signal Transduction - drug effects; Histone deacetylase; Hydrazide; Clinical trials; Hydroxamic acid; Benzamide; Sirtuin; p53; Posttranslational modification; Tetrapeptide; Depsipeptide; Lysine; HDAC inhibitor; Amino-benzamide; Short-chain fatty acid; Acetylation; NCI 60 cell line screen; Pharmacokinetics; Acylation
• ISSN: 2162-5557; 2162-5557
• DOI: 10.1016/bs.acr.2018.02.006

Since the identification and cloning of human histone deacetylases (HDACs) and the rapid approval of vorinostat (Zolinza®) for the treatment of cutaneous T-cell lymphoma, the field of HDAC biology has met many initial successes. However, many challenges remain due to the complexity involved in the lysine posttranslational modifications, epigenetic transcription regulation, and nonepigenetic cellular signaling cascades. In this chapter, we will: review the discovery of the first HDAC inhibitor and present discussion regarding the future of next-generation HDAC inhibitors, give an overview of different classes of HDACs and their differences in lysine deacylation activity, discuss different classes of HDAC inhibitors and their HDAC isozyme preferences, and review HDAC inhibitors' preclinical studies, their clinical trials, their pharmacokinetic challenges, and future direction. We will also discuss the likely reason for the failure of multiple HDAC inhibitor clinical trials in malignancies other than lymphoma and multiple myeloma. In addition, the potential molecular mechanism(s) that may play a key role in the efficacy and therapeutic response rate in the clinic and the likely patient population for HDAC therapy will be discussed.