نتایج جستجو برای: hdac

تعداد نتایج: 4231  

Journal: :Anti-cancer drugs 2005
Sybille Wittich Hans Scherf Changping Xie Birgit Heltweg Franck Dequiedt Eric Verdin Clarissa Gerhäuser Manfred Jung

Histone deacetylase (HDAC) inhibitors are a novel class of promising anti-cancer agents. Little information is available on the capacity of structurally different HDAC inhibitors to induce terminal cell differentiation in different cell types in relation to enzyme inhibition and subtype selectivity. Consequently, the aim of this study was to provide a comprehensive comparison of these effects. ...

Journal: :American journal of physiology. Heart and circulatory physiology 2007
Tsung-Ming Lee Mei-Shu Lin Nen-Chung Chang

Histone deacetylase (HDAC) determines the acetylation status of histones and, thereby, controls the regulation of gene expression. HDAC inhibitors have been shown to inhibit cardiomyocyte growth in vitro and in vivo. We assessed whether HDAC inhibitors exert a beneficial effect on the remodeling heart in infarcted rats. At 24 h after ligation of the left anterior descending artery, male Wistar ...

Journal: :Molecular cancer therapeutics 2009
John P Alao Jeanette Olesch Per Sunnerhagen

Histone deacetylase (HDAC) inhibitors potently inhibit tumor growth and are currently being evaluated for their efficacy as chemosensitizers and radiosensitizers. This efficacy is likely to be limited by the fact that HDAC inhibitors also induce cell cycle arrest. Deletion of the class I HDAC Rpd3 has been shown to specifically suppress the sensitivity of Saccharomyces cerevisiae DNA damage che...

Journal: :Molecular cancer therapeutics 2008
Marielle Fournel Claire Bonfils Yu Hou Pu Theresa Yan Marie-Claude Trachy-Bourget Ann Kalita Jianhong Liu Ai-Hua Lu Nancy Z Zhou Marie-France Robert Jeffrey Gillespie James J Wang Hélène Ste-Croix Jubrail Rahil Sylvain Lefebvre Oscar Moradei Daniel Delorme A Robert Macleod Jeffrey M Besterman Zuomei Li

Nonselective inhibitors of human histone deacetylases (HDAC) are known to have antitumor activity in mice in vivo, and several of them are under clinical investigation. The first of these, Vorinostat (SAHA), has been approved for treatment of cutaneous T-cell lymphoma. Questions remain concerning which HDAC isotype(s) are the best to target for anticancer activity and whether increased efficacy...

2012
Katherine T. Andrews Archna P. Gupta Thanh N. Tran David P. Fairlie Geoffrey N. Gobert Zbynek Bozdech

Histone deacetylase (HDAC) inhibitors are being intensively pursued as potential new drugs for a range of diseases, including malaria. HDAC inhibitors are also important tools for the study of epigenetic mechanisms, transcriptional control, and other important cellular processes. In this study the effects of three structurally related antimalarial HDAC inhibitors on P. falciparum malaria parasi...

2016
Leonid A. Serebryannyy Christina M. Cruz Primal de Lanerolle

Class I histone deacetylases (HDACs) are known to remove acetyl groups from histone tails. This liberates positive charges on the histone tail and allows for tighter winding of DNA, preventing transcription factor binding and gene activation. Although the functions of HDAC proteins are becoming apparent both biochemically and clinically, how this class of proteins is regulated remains poorly un...

Journal: :Genes & development 1999
T Nomura M M Khan S C Kaul H D Dong R Wadhwa C Colmenares I Kohno S Ishii

The N-CoR/SMRT complex containing mSin3 and histone deacetylase (HDAC) mediates transcriptional repression by nuclear hormone receptors and Mad. The proteins encoded by the ski proto-oncogene family directly bind to N-CoR/SMRT and mSin3A, and forms a complex with HDAC. c-Ski and its related gene product Sno are required for transcriptional repression by Mad and thyroid hormone receptor (TRbeta)...

2010
Tomoko Kawabata Keiichiro Nishida Koji Takasugi Hiroko Ogawa Kenei Sada Yasutaka Kadota Junko Inagaki Satoshi Hirohata Yoshifumi Ninomiya Hirofumi Makino

INTRODUCTION The purpose of this study was to investigate the profile of histone deacetylase (HDAC) expression in the synovial tissue of rheumatoid arthritis (RA) compared with that of normal control and osteoarthritis (OA), and to examine whether there is a link between HDAC activity and synovial inflammation. METHODS HDAC activity and histone acetyltransferase (HAT) activity were determined...

Journal: :Cardiovascular research 2007
Ting C Zhao Guangmao Cheng Ling X Zhang Yi T Tseng James F Padbury

OBJECTIVES Recent evidence has demonstrated the importance of histone deacetylases (HDAC) in the control of hypertrophic responses in the heart. However, it remains unknown whether inhibition of HDACs plays a role in myocardial ischemia and reperfusion (I/R) injury. We hypothesize that HDAC inhibition triggers preconditioning-like effects against I/R injury. METHODS AND RESULTS Isolated mouse...

2014
Xingsheng Hu Lin Wang Lin Lin Yuankai Shi

Histone deacetylase (HDAC) inhibitors, which represent a structurally diverse group of molecules, have emerged as a novel therapeutic class of molecules with significant anticancer potential. Vorinostat and romidepsin, known as the first generation of HDAC inhibitors, were approved in the United States for the treatment of T-cell lymphomas. Preliminary activity of HDAC inhibitors has also been ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید