The DOI matches its Crossref record; 22 of the 22 references it cites were found in a registry or an index.
Histone deacetylation in epigenetics: An attractive target for anticancer therapy
Abstract
The reversible histone acetylation and deacetylation are epigenetic phenomena that play critical roles in the modulation of chromatin topology and the regulation of gene expression. Aberrant transcription due to altered expression or mutation of genes that encode histone acetyltransferase (HAT) or histone deacetylase (HDAC) enzymes or their binding partners, has been clearly linked to carcinogenesis. The histone deacetylase inhibitors are a new promising class of anticancer agents (some of which in clinical trials), that inhibit the proliferation of tumor cells in culture and in vivo by inducing cell-cycle arrest, terminal differentiation, and/or apoptosis. This report reviews the chemistry and the biology of HDACs and HDAC inhibitors, laying particular emphasis on agents actually in clinical trials for cancer therapy and on new potential anticancer lead compounds more selective and less toxic.
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Cites
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Cited by
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Self-citationDevelopment of Dual Inhibitors Targeting Epidermal Growth Factor Receptor in Cancer Therapy
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Self-citationEngaging plasticity: Differentiation therapy in solid tumors
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Metadata
- Authors
- Mai, A., Massa, S., Rotili, D., Cerbara, I., Valente, S., Pezzi, R., Simeoni, S., & Ragno, R.
- Venue
- Medicinal Research Reviews
- Publisher
- Wiley
- Published
- 2005
- Volume
- 25
- Issue
- 3
- Pages
- 261-309
- ISSN
- 0198-6325 (ISSN-L)
- 1098-1128
- OpenAlex
- W2104600818
- Cited by
- 319
- References
- 22
- FWCI
- 8.41
- Type
- journal article
- Language
- en
- Open access
- closed
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