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Cell Cycle. 2004 May;3(5):534-5. Epub 2004 May 4.

The mechanism of the anti-tumor activity of the histone deacetylase inhibitor, suberoylanilide hydroxamic acid (SAHA).

Author information

1
Memorial Sloan-Kettering Cancer Center, New York City, New York 10021, USA. PaulA_Marks@mskcc.org

Abstract

Histone deacetylases (HDAC) are ubiquitously distributed through chromatin. Nevertheless HDAC inhibitors (HDACi), such as SAHA, selectively alter the transcription of as few as 2-5% of expressed genes in various transformed cells. p21(WAF1) is one of the most commonly induced genes in cells cultured with SAHA. Understanding the mechanism of the selective effects of the HDACi is a challenging problem. Gui et al. have identified effects of SAHA on p21(WAF1) promotor associated proteins that explain, at least in part, the selective effects of HDAC in altering gene expression.

PMID:
15020838
DOI:
10.4161/cc.3.5.827
[Indexed for MEDLINE]

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