Antitumor activity of the histone deacetylase inhibitor MS‐275 in prostate cancer models
BACKGROUND Histone deacetylase (HDAC) inhibitors represent a novel class of
therapeutic agents with antitumor activity currently in clinical development. In this study, we …
therapeutic agents with antitumor activity currently in clinical development. In this study, we …
A novel histone deacetylase (HDAC) inhibitor MHY219áinduces apoptosis via up-regulation of androgen receptor expression in human prostate cancer cells
N Patra, U De, TH Kim, YJ Lee, MY Ahn, ND Kim… - Biomedicine & …, 2013 - Elsevier
Histone deacetylase (HDAC) inhibitors are a new class of anticancer agents that act by
inhibiting cancer cell proliferation and inducing apoptosis in various cancer cell lines. To …
inhibiting cancer cell proliferation and inducing apoptosis in various cancer cell lines. To …
Antitumor Effects of a Novel Phenylbutyrate-Based Histone Deacetylase Inhibitor, (S)-HDAC-42, in Prostate Cancer
SK Kulp, CS Chen, DS Wang, CY Chen… - Clinical Cancer Research, 2006 - AACR
Purpose: To assess the antitumor effects of a novel phenylbutyrate-derived histone
deacetylase (HDAC) inhibitor,(S)-HDAC-42, vis-à-vis suberoylanilide hydroxamic acid …
deacetylase (HDAC) inhibitor,(S)-HDAC-42, vis-à-vis suberoylanilide hydroxamic acid …
New histone deacetylase inhibitors as potential therapeutic tools for advanced prostate carcinoma
SA Wedel, A Sparatore, PD Soldato… - Journal of cellular …, 2008 - Wiley Online Library
The anti‐epileptic drug valproic acid is also under trial as an anti‐cancer agent due to its
histone deacetylase (HDAC) inhibitory properties. However, the effects of valproic acid …
histone deacetylase (HDAC) inhibitory properties. However, the effects of valproic acid …
Cytostatic action of novel histone deacetylase inhibitors in androgen receptor-null prostate cancer cells
Androgen receptor (AR)-null prostate tumors have been observed in 11–24% of patients.
Histone deacetylases (HDACs) are overexpressed in prostate tumors. Therefore, HDAC …
Histone deacetylases (HDACs) are overexpressed in prostate tumors. Therefore, HDAC …
[HTML][HTML] A new histone deacetylase inhibitor, MHY219, inhibits the migration of human prostate cancer cells via HDAC1
U De, S Kundu, N Patra, MY Ahn, JH Ahn… - Biomolecules & …, 2015 - ncbi.nlm.nih.gov
Histone deacetylase (HDAC) inhibitors are considered novel agents for cancer
chemotherapy. We previously investigated MHY219, a new HDAC inhibitor, and its potent …
chemotherapy. We previously investigated MHY219, a new HDAC inhibitor, and its potent …
Differential effects of PXD101 (belinostat) on androgen-dependent and androgen-independent prostate cancer models
GL Gravina, F Marampon, I Giusti… - International …, 2012 - spandidos-publications.com
Histone deacetylase inhibitors (HDACi) are promising epigenetic cancer chemotherapeutics
rapidly approaching clinical use. In this study, we tested using in vitro and in vivo models the …
rapidly approaching clinical use. In this study, we tested using in vitro and in vivo models the …
Effectiveness of the histone deacetylase inhibitor (S)-2 against LNCaP and PC3 human prostate cancer cells
A Laurenzana, M Balliu, C Cellai, MN Romanelli… - PloS one, 2013 - journals.plos.org
Histone deacetylase inhibitors (HDACi) represent a promising class of epigenetic agents
with anticancer properties. Here, we report that (S)-2, a novel hydroxamate-based HDACi …
with anticancer properties. Here, we report that (S)-2, a novel hydroxamate-based HDACi …
Activity of the histone deacetylase inhibitor belinostat (PXD101) in preclinical models of prostate cancer
X Qian, G Ara, E Mills, WJ LaRochelle… - … journal of cancer, 2008 - Wiley Online Library
Histone deacetylase inhibitors (HDACi) represent a promising new class of anticancer
agents. In the current investigation, we examined the activity of the HDACi belinostat in …
agents. In the current investigation, we examined the activity of the HDACi belinostat in …
Antitumor effects of a novel sulfur‐containing hydroxamate histone deacetylase inhibitor H40
J Long, J Zhao, Z Yan, Z Liu… - International journal of …, 2009 - Wiley Online Library
Histone deacetylase (HDAC) inhibitors are among the most promising targeted anticancer
agents and are potent inducers of growth arrest, differentiation, and/or apoptotic cell death of …
agents and are potent inducers of growth arrest, differentiation, and/or apoptotic cell death of …