Histone deacetylases and cancer: causes and therapies

PA Marks, RA Rifkind, VM Richon, R Breslow… - Nature Reviews …, 2001 - nature.com
Together, histone acetyltransferases and histone deacetylases (HDACs) determine the
acetylation status of histones. This acetylation affects the regulation of gene expression, and …

Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells

PA Marks, VM Richon, RA Rifkind - Journal of the National …, 2000 - academic.oup.com
Histone deacetylase (HDAC) inhibitors have been shown to be potent inducers of growth
arrest, differentiation, and/or apoptotic cell death of transformed cells in vitro and in vivo. One …

Histone deacetylase (HDAC) inhibitor activation of p21WAF1 involves changes in promoter-associated proteins, including HDAC1

CY Gui, L Ngo, WS Xu, VM Richon… - Proceedings of the …, 2004 - National Acad Sciences
Histone deacetylase (HDAC) inhibitors (HDACi) cause cancer cell growth arrest and/or
apoptosis in vivo and in vitro. The HDACi suberoylanilide hydroxamic acid (SAHA) is in …

Histone deacetylase (HDAC) inhibitors in recent clinical trials for cancer therapy

K Keller, M Jung - Epigenetic Therapy of Cancer: Preclinical Models and …, 2013 - Springer
Histone deacetylases are key enzymes of epigenetic regulation and are therefore involved
in crucial cellular events like transcription, differentiation, apoptosis and cell division. The …

Histone deacetylase inhibitor induces DNA damage, which normal but not transformed cells can repair

JH Lee, ML Choy, L Ngo, SS Foster… - Proceedings of the …, 2010 - National Acad Sciences
Histone deacetylase inhibitors (HDACi) developed as anti-cancer agents have a high
degree of selectivity for killing cancer cells. HDACi induce acetylation of histones and …

Suberoylanilide Hydroxamic Acid, an Inhibitor of Histone Deacetylase, Suppresses the Growth of Prostate Cancer Cells in Vitro and in Vivo

LM Butler, DB Agus, HI Scher, B Higgins, A Rose… - Cancer research, 2000 - AACR
Suberoylanilide hydroxamic acid (SAHA) is the prototype of a family of hybrid polar
compounds that induce growth arrest in transformed cells and show promise for the …

A novel mechanism of chemoprotection by sulforaphane: inhibition of histone deacetylase

MC Myzak, PA Karplus, FL Chung, RH Dashwood - Cancer research, 2004 - AACR
Sulforaphane (SFN), a compound found at high levels in broccoli and broccoli sprouts, is a
potent inducer of phase 2 detoxification enzymes and inhibits tumorigenesis in animal …

The histone deacetylase inhibitor SAHA arrests cancer cell growth, up-regulates thioredoxin-binding protein-2, and down-regulates thioredoxin

LM Butler, X Zhou, WS Xu, HI Scher… - Proceedings of the …, 2002 - National Acad Sciences
Suberoylanilide hydroxamic acid (SAHA) is a potent inhibitor of histone deacetylases
(HDACs) that causes growth arrest, differentiation, and/or apoptosis of many tumor types in …

Gene expression profiling of multiple histone deacetylase (HDAC) inhibitors: defining a common gene set produced by HDAC inhibition in T24 and MDA carcinoma …

KB Glaser, MJ Staver, JF Waring, J Stender… - Molecular cancer …, 2003 - AACR
Acetylation of histones in chromatin is one mechanism involved in the regulation of gene
transcription and is tightly controlled by the balance of acetyltransferase and deacetylase …

Histone deacetylase inhibitors.

PA Marks, VM Richon, T Miller… - Advances in cancer …, 2004 - europepmc.org
The base sequence of DNA provides the genetic code for proteins. The regulation of
expression or suppression of gene transcription is largely determined by the structure of the …