Literature DB >> 22876951

Histone deacetylases as targets for multiple diseases.

Jaiprakash N Sangshetti1, Nikhil S Sakle, M H G Dehghan, Devanand B Shinde.   

Abstract

Inhibition of Histone deacetylases (HDACs) has been emerged as important approach to reverse aberrant epigenetic changes associated with various cancerous and non-cancerous diseases. The field of histone deacetylase inhibitors (HDIs) is moving into a new phase of development. The structure of histone deacetylases is well-established and the active sites have been well identified. Various drugs targeting this enzyme are in the pipeline for the treatment of different diseases. Since first-generation HDAC inhibitors proved their clinical fruitfulness and also second generation inhibitors are rationally designed with improved specificity, experts believe that this class will emerge in the treatment of various diseases. Considering these facts present review focuses on HDACs and developments of HDIs in the treatment of various diseases.

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Year:  2013        PMID: 22876951     DOI: 10.2174/1389557511313070006

Source DB:  PubMed          Journal:  Mini Rev Med Chem        ISSN: 1389-5575            Impact factor:   3.862


  3 in total

Review 1.  Targeting Brd4 for cancer therapy: inhibitors and degraders.

Authors:  Yingchao Duan; Yuanyuan Guan; Wenping Qin; Xiaoyu Zhai; Bin Yu; Hongmin Liu
Journal:  Medchemcomm       Date:  2018-08-07       Impact factor: 3.597

Review 2.  Biological approaches for hypertrophic scars.

Authors:  Zhong Lingzhi; Li Meirong; Fu Xiaobing
Journal:  Int Wound J       Date:  2019-12-20       Impact factor: 3.315

3.  Overexpression of HDAC9 is associated with poor prognosis and tumor progression of breast cancer in Chinese females.

Authors:  Yixiang Huang; Wei Jian; Junyong Zhao; Gang Wang
Journal:  Onco Targets Ther       Date:  2018-04-17       Impact factor: 4.147

  3 in total

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