| Literature DB >> 32454703 |
Rakesh Yadav1, Pooja Mishra1, Divya Yadav1.
Abstract
Cancer is a provocative issue across the globe and treatment of uncontrolled cell growth follows a deep investigation in the field of drug discovery. Therefore, there is a crucial requirement for discovering an ingenious medicinally active agent that can amend idle drug targets. Increasing pragmatic evidence implies that histone deacetylases (HDACs) are trapped during cancer progression, which increases deacetylation and triggers changes in malignancy. They provide a ground-breaking scaffold and an attainable key for investigating chemical entity pertinent to HDAC biology as a therapeutic target in the drug discovery context. Due to gene expression, an impending requirement to prudently transfer cytotoxicity to cancerous cells, HDAC inhibitors may be developed as anticancer agents. The present review focuses on the basics of HDAC enzymes, their inhibitors, and therapeutic outcomes. ©Copyright 2019 Turk J Pharm Sci, Published by Galenos Publishing House.Entities:
Keywords: Histone deacetylase inhibitors; apoptosis; cancer; multitherapeutic approach
Year: 2018 PMID: 32454703 PMCID: PMC7227979 DOI: 10.4274/tjps.75047
Source DB: PubMed Journal: Turk J Pharm Sci ISSN: 1304-530X