نتایج جستجو برای: histon deacetylas inhibitors hdaci

تعداد نتایج: 188850  

Journal: :Nutrition and cancer 2012
Mohammed O Altonsy Tito N Habib Simon C Andrews

The health benefits of garlic have been proven by epidemiological and experimental studies. Diallyl disulphide (DADS), the major organosulfur compound found in garlic oil, is known to lower the incidence of breast cancer both in vitro and in vivo. The studies reported here demonstrate that DADS induces apoptosis in the MCF-7 breast-cancer cell line through interfering with cell-cycle growth pha...

2016
Madhura G. Kelkar Kalimuthu Senthilkumar Smita Jadhav Sudeep Gupta Beyong-Cheol Ahn Abhijit De

The aberrant expression of human sodium iodide symporter (NIS) in breast cancer (BC) has raised the possibility of using targeted radioiodide therapy. Here we investigate modulation of endogenous, functional NIS expression by histone deacetylase inhibitors (HDACi) in vitro and in vivo. Luciferase reporter based initial screening of six different HDACi shows 2-10 fold enhancement of NIS promoter...

2011
Luca A. Petruccelli Daphné Dupéré-Richer Filippa Pettersson Hélène Retrouvey Sophia Skoulikas Wilson H. Miller

Histone deacetylase inhibitors (HDACi) are promising anti-cancer agents, however, their mechanisms of action remain unclear. In acute myeloid leukemia (AML) cells, HDACi have been reported to arrest growth and induce apoptosis. In this study, we elucidate details of the DNA damage induced by the HDACi vorinostat in AML cells. At clinically relevant concentrations, vorinostat induces double-stra...

Journal: :Molecular cancer therapeutics 2010
Ruman Rahman Teresa Osteso-Ibanez Robert A Hirst Jane Levesley John-Paul Kilday Siobhan Quinn Andrew Peet Chris O'Callaghan Beth Coyle Richard G Grundy

Aberrant epigenetic regulation of gene expression contributes to tumor initiation and progression. Studies from a plethora of hematologic and solid tumors support the use of histone deacetylase inhibitors (HDACi) as potent anticancer agents. However, the mechanism of HDACi action with respect to the temporal order of induced cellular events is unclear. The present study investigates the antican...

Journal: :Molecular pharmacology 2010
Keeming Chia Heather Beamish Kaneez Jafferi Brian Gabrielli

Histone deacetylase inhibitors (HDACis) are currently in trial or are in clinical use for the treatment of a number of tumor types. The clinical efficacy of HDACis can be partly attributed to the modulation of the cell cycle by the HDACis. Here, we have examined the effects of N-(2-aminophenyl)-4-((4-pyridin-3-ylpyrimidin-2-ylamino)methyl)benzamide (MGCD0103), a class I-selective histone deacet...

2011
Valentina Zuco Michelandrea De Cesare Raffaella Cincinelli Raffaella Nannei Claudio Pisano Nadia Zaffaroni Franco Zunino

Preclinical studies support the therapeutic potential of histone deacetylases inhibitors (HDACi) in combination with taxanes. The efficacy of combination has been mainly ascribed to a cooperative effect on microtubule stabilization following tubulin acetylation. In the present study we investigated the effect of paclitaxel in combination with two novel HDACi, ST2782 or ST3595, able to induce p5...

2015
Afua Adjeiwaa Mensah Ivo Kwee Eugenio Gaudio Andrea Rinaldi Maurilio Ponzoni Luciano Cascione Gianluca Fossati Anastasios Stathis Emanuele Zucca Gianluca Caprini Francesco Bertoni

We investigated the pre-clinical activities of two novel histone deacetylase inhibitors (HDACi), ITF-A and ITF-B, in a large panel of pre-clinical lymphoma models. The two compounds showed a dose-dependent anti-proliferative activity in the majority of cell lines. Gene expression profiling (GEP) of diffuse large B-cell lymphoma (DLBCL) cells treated with the compounds showed a modulation of gen...

Journal: :Cancer research 2009
Xiaoping Huang Lizhi Gao Shuiliang Wang Choon-Kee Lee Peter Ordentlich Bolin Liu

Breast cancer is a highly heterogeneous disease with distinct histologic subtypes. Targeted therapies such as endocrine therapy and growth factor receptor inhibitors have had a significant impact on the treatment of metastatic breast cancer patients. Unfortunately, resistance to these agents eventually occurs, and currently represents a significant clinical problem in the management of breast c...

Journal: :Human molecular genetics 2009
Lutz Garbes Markus Riessland Irmgard Hölker Raoul Heller Jan Hauke Christian Tränkle Roland Coras Ingmar Blümcke Eric Hahnen Brunhilde Wirth

Histone deacetylase inhibitors (HDACi) are potential candidates for therapeutic approaches in cancer and neurodegenerative diseases such as spinal muscular atrophy (SMA)--a common autosomal recessive disorder and frequent cause of early childhood death. SMA is caused by homozygous absence of SMN1. Importantly, all SMA patients carry a nearly identical copy gene, SMN2, that produces only minor l...

2017
Rosalie M. Sterner Kimberly N. Kremer Aref Al-Kali Mrinal M. Patnaik Naseema Gangat Mark R. Litzow Scott H. Kaufmann Jennifer J. Westendorf Andre J. van Wijnen Karen E. Hedin

The bone marrow microenvironment protects acute myeloid leukemia (AML) cells during chemotherapy and is a major factor in relapse. Here, we examined which type(s) of bone marrow cells are responsible for the relapse of AML following treatment with cytarabine (Ara-C), and we identified a means to inhibit this protection. To determine the protective cell type(s), AML cells were treated with Ara-C...

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