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HDACi--going through the mechanisms
- Source :
- Frontiers in bioscience (Landmark edition). 16(1)
- Publication Year :
- 2011
-
Abstract
- 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.
- Subjects :
- Antineoplastic Agents
Apoptosis
Histone Deacetylases
Epigenesis, Genetic
Histones
Neoplasms
Gene expression
Autophagy
Humans
Tumor Protein p73
Epigenetics
HSP90 Heat-Shock Proteins
Enzyme Inhibitors
Transcription factor
Epigenesis
Histone Acetyltransferases
Clinical Trials as Topic
biology
Neovascularization, Pathologic
Tumor Suppressor Proteins
Cell Cycle
Nuclear Proteins
Combined Modality Therapy
Chromatin
DNA-Binding Proteins
Histone Deacetylase Inhibitors
Histone
DNA Repair Enzymes
Matrix Metalloproteinase 9
Acetylation
Cancer research
biology.protein
Matrix Metalloproteinase 2
Tumor Suppressor Protein p53
Reactive Oxygen Species
Protein Processing, Post-Translational
Subjects
Details
- ISSN :
- 27686698
- Volume :
- 16
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Frontiers in bioscience (Landmark edition)
- Accession number :
- edsair.doi.dedup.....4bc6be67d8d54adcd0d5f7723b765e31