2008Chinese Journal of New Drugs and Clinical RemediesRequires access

Update of histone deacetylase inhibitors

Xudong Ma

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Abstract

Histone deacetylase(HDAC)inhibitors contain a functional group,which mimics lysine side chain that interacts with the critical HDAC Zinc atom.They are able to up-regulate histone acetylation and down- regulate deacetylation via competitive inhibition to modulate the gene transcription and expression,inhibit cell proliferation,stimulate cell differentiation,and provocate cell apoptosis.Many HDAC inhibitors have been found or synthesized as new potent anticancer drugs.

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What this paper is about

Histone deacetylase(HDAC)inhibitors contain a functional group,which mimics lysine side chain that interacts with the critical HDAC Zinc atom.They are able to up-regulate histone acetylation and down- regulate deacetylation via competitive inhibition to modulate the gene transcription and expression,inhibit cell proliferation,stimulate cell differentiation,and provocate cell apoptosis.Many HDAC inhibitors have been found or synthesized as new potent anticancer drugs.

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Available abstract

Histone deacetylase(HDAC)inhibitors contain a functional group,which mimics lysine side chain that interacts with the critical HDAC Zinc atom.They are able to up-regulate histone acetylation and down- regulate deacetylation via competitive inhibition to modulate the gene transcription and expression,inhibit cell proliferation,stimulate cell differentiation,and provocate cell apoptosis.Many HDAC inhibitors have been found or synthesized as new potent anticancer drugs.

Key concepts: Histone deacetylase, Histone deacetylase 5, HDAC11, Acetylation, Histone deacetylase 2, HDAC1, Chemistry, HDAC4

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