Histone Deacetylases as Targets for Multiple Diseases

被引:0
作者
Sangshetti, Jaiprakash N. [1 ]
Sakle, Nikhil S. [1 ]
Dehghan, M. H. G. [1 ]
Shinde, Devanand B. [2 ]
机构
[1] YB Chavan Coll Pharm, Aurangabad 431001, Maharashtra, India
[2] Dr BAM Univ, Dept Chem Technol, Aurangabad 431004, Maharashtra, India
关键词
Histone deacetylase; Cancer; Non-cancer disorders; CANCER CELL-LINES; ACTIVITY IN-VITRO; ANTITUMOR-ACTIVITY; GENE-EXPRESSION; CYCLIC TETRAPEPTIDE; TRICHOSTATIN-A; LIFE-SPAN; ANTICANCER AGENTS; MYELOID-LEUKEMIA; TUMOR-CELLS;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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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页码:1005 / 1026
页数:22
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