| Literature DB >> 31309879 |
Dimitrios Schizas1, Aikaterini Mastoraki2, Leon Naar2, Diamantis I Tsilimigras3, Ioannis Katsaros1, Vasiliki Fragkiadaki4, Georgia-Sofia Karachaliou5, Nikolaos Arkadopoulos2, Theodore Liakakos1, Dimitrios Moris6.
Abstract
Chemotherapy resistance is a rising concern in Gastric Cancer (GC) and has led to the investigation of various cellular compounds. Α functional equilibrium of histone acetylation and deacetylation was discovered in all cells, regulated by Histone Acetyltransferases and Deacetylases (HDACs), controlling chromatin coiling status and changing gene expression appropriately. In accordance with recent research, this equilibrium can be dysregulated in cancer cells aiding in the process of carcinogenesis and tumor progression by altering histone and non-histone proteins affecting gene expression, cell cycle control, differentiation, and apoptosis in various malignancies. In addition, increased HDAC expression in GC cells has been associated with increased stage, tumor invasion, nodal metastases, increased distant metastatic potential, and decreased overall survival. HDAC inhibitors could be used as treatment regimens for GC patients and could develop important synergistic interactions with chemotherapy drugs. The aim of this article is to review the molecular identity and mechanism of action of HDAC inhibitors, as well as highlight their potential utility as anti-cancer agents in GC. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: HDACs; biochemical identity; chemotherapy resistance; drug discovery; gastric cancer; multi-disciplinary approach
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Year: 2020 PMID: 31309879 DOI: 10.2174/0929867326666190712160842
Source DB: PubMed Journal: Curr Med Chem ISSN: 0929-8673 Impact factor: 4.530