
doi: 10.2741/3691
pmid: 21196174
Histone deacetylases inhibitors (HDACi) have recently emerged as potent antitumor treatment modality. They are currently tested in many phase I, II and III clinical trials as single agents as wells as in combination schemes. They have demonstrated promising antitumor activity and favorable clinical outcome. Histone deacetylases (HDACs) are involved in the process of epigenetic regulation of gene expression. Epigenetic changes are believed to be crucial for the onset and progression of cancer and have recently gained remarkable attention. Since epigenetic regulation of gene expression is a reversible process, targeting histone deacetylases provides a good rationale for anticancer therapy. The acetylation status of histones regulates the organization of chromatin and the access of transcription factors. Moreover, functions of many non-histone proteins are controlled by acetylation. The broad and complicated influences of HDACi on various molecular processes may account for the observed pleiotropic effects. In this review we summarize recent advances in the understanding of biology of HDACs and mechanism of action of their inhibitors.
Clinical Trials as Topic, Neovascularization, Pathologic, Cell Cycle, Antineoplastic Agents, Apoptosis, Combined Modality Therapy, Histone Deacetylases, Epigenesis, Genetic, DNA-Binding Proteins, Histone Deacetylase Inhibitors, Histones, DNA Repair Enzymes, Matrix Metalloproteinase 9, Neoplasms, Autophagy, Humans, Matrix Metalloproteinase 2, HSP90 Heat-Shock Proteins, Enzyme Inhibitors, Histone Acetyltransferases
Clinical Trials as Topic, Neovascularization, Pathologic, Cell Cycle, Antineoplastic Agents, Apoptosis, Combined Modality Therapy, Histone Deacetylases, Epigenesis, Genetic, DNA-Binding Proteins, Histone Deacetylase Inhibitors, Histones, DNA Repair Enzymes, Matrix Metalloproteinase 9, Neoplasms, Autophagy, Humans, Matrix Metalloproteinase 2, HSP90 Heat-Shock Proteins, Enzyme Inhibitors, Histone Acetyltransferases
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