نتایج جستجو برای: suberoylanilide hydroxamic acid saha

تعداد نتایج: 748959  

Journal: :Molecular medicine 2000
L Huang A B Pardee

BACKGROUND Suberoylanilide hydroxamic acid (SAHA) is a prototype of the newly developed, second-generation, hybrid polar compounds. It is a novel histone deacetylase inhibitor with high potency for inducing cell differentiation of cultured murine erythroleukemia cells. Studies with SAHA have primarily been performed with hematopoietic tumor cells. Here we extent these studies with SAHA to human...

Journal: :Journal of neurochemistry 2015
Carolina Alquézar Estíbaliz Barrio Noemí Esteras Ana de la Encarnación Fernando Bartolomé José A Molina Ángeles Martín-Requero

At present, treatment for Parkinson's disease (PD) is only symptomatic; therefore, it is important to identify new targets tackling the molecular causes of the disease. We previously found that lymphoblasts from sporadic PD patients display increased activity of the cyclin D3/CDK6/pRb pathway and higher proliferation than control cells. These features were considered systemic manifestations of ...

2015
Terra Vleeshouwer-Neumann Michael Phelps Theo K. Bammler James W. MacDonald Isaac Jenkins Eleanor Y. Chen Javier S Castresana

Embryonal rhabdomyosarcoma (ERMS) is the most common soft tissue cancer in children. The prognosis of patients with relapsed or metastatic disease remains poor. ERMS genomes show few recurrent mutations, suggesting that other molecular mechanisms such as epigenetic regulation might play a major role in driving ERMS tumor biology. In this study, we have demonstrated the diverse roles of histone ...

Journal: :Molecular cancer therapeutics 2012
Pete Taylor Jason Fangusaro Veena Rajaram Stewart Goldman Irene B Helenowski Tobey MacDonald Martin Hasselblatt Lars Riedemann Alvaro Laureano Laurence Cooper Vidya Gopalakrishnan

Medulloblastoma is a malignant pediatric brain tumor. Current treatment following patient stratification into standard and high-risk groups using clinical features has improved survival. However, a subset of patients with standard risk features have unanticipated aggressive disease, underscoring the need for a better understanding of tumor biology and the development of novel treatments. Poor d...

Journal: :International journal of oncology 2008
D Carlisi B Vassallo M Lauricella S Emanuele A D'Anneo E Di Leonardo P Di Fazio R Vento G Tesoriere

This report shows that histone deacetylase inhibitors (HDACIs) induced apoptosis in human hepatoma HepG2 cells in a dose- and time-dependent manner. Trichostatin A (TSA), ITF2357 and suberoylanilide hydroxamic acid (SAHA), which were very effective agents, caused apoptotic effects after a lag phase of 12-16 h. In order to elucidate the mechanism of HDACIs action in HepG2 cells we have studied t...

2016
Subhash Haldar Christopher Dru Rajeev Mishra Manisha Tripathi Frank Duong Bryan Angara Ana Fernandez Moshe Arditi Neil A. Bhowmick

Hemorrhagic cystitis is an inflammatory and ulcerative bladder condition associated with systemic chemotherapeutics, like cyclophosphomide. Earlier, we reported reactive oxygen species resulting from cyclophosphamide metabolite, acrolein, causes global methylation followed by silencing of DNA damage repair genes. Ogg1 (8-oxoguanine DNA glycosylase) is one such silenced base excision repair enzy...

2017
Zijun Zhen Kaibin Yang Litong Ye Zhiyao You Rirong Chen Ying Liu Youjian He

Paclitaxel is not as effective for neuroblastoma as most of the front-line chemotherapeutics due to drug resistance. This study explored the regulatory mechanism of paclitaxel-associated autophagy and potential solutions to paclitaxel resistance in neuroblastoma. The formation of autophagic vesicles was detected by scanning transmission electron microscopy and flow cytometry. The autophagy-asso...

2014
Tao Zhang Yihua Chen Jingjie Li Feifei Yang Haigang Wu Fujun Dai Meichun Hu Xiaoling Lu Yi Peng Mingyao Liu Yongxiang Zhao Zhengfang Yi

Accumulating evidence demonstrates important roles for histone deacetylase in tumorigenesis (HDACs), highlighting them as attractive targets for antitumor drug development. Histone deactylase inhibitors (HDACIs), which have shown favorable anti-tumor activity with low toxicity in clinical investigations, are a promising class of anticancer therapeutics. Here, we screened our compound library to...

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