نتایج جستجو برای: epothilone a

تعداد نتایج: 13431870  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2001
F Y Lee R Borzilleri C R Fairchild S H Kim B H Long C Reventos-Suarez G D Vite W C Rose R A Kramer

BMS-247550, a novel epothilone derivative, is being developed by Bristol-Myers Squibb Company (BMS) as an anticancer agent for the treatment of patients with malignant tumors. BMS-247550 is a semisynthetic analogue of the natural product epothilone B and has a mode of action analogous to that of paclitaxel (i.e., microtubule stabilization). In vitro, it is twice as potent as paclitaxel in induc...

Journal: :Cancer research 2008
Jens Hoffmann Ilio Vitale Bernd Buchmann Lorenzo Galluzzi Wolfgang Schwede Laura Senovilla Werner Skuballa Sonia Vivet Rosemarie B Lichtner José M Vicencio Theocharis Panaretakis Gerhard Siemeister Hermann Lage Lisa Nanty Stefanie Hammer Kevin Mittelstaedt Sebastian Winsel Julia Eschenbrenner Maria Castedo Carine Demarche Ulrich Klar Guido Kroemer

Sagopilone (ZK-EPO) is the first fully synthetic epothilone undergoing clinical trials for the treatment of human tumors. Here, we investigate the cellular pathways by which sagopilone blocks tumor cell proliferation and compare the intracellular pharmacokinetics and the in vivo pharmacodynamics of sagopilone with other microtubule-stabilizing (or tubulin-polymerizing) agents. Cellular uptake a...

2010
Patrick A. Ott Anne Hamilton Amanda Jones Naomi Haas Tsiporah Shore Sandra Liddell Paul J. Christos L. Austin Doyle Michael Millward Franco M. Muggia Anna C. Pavlick

BACKGROUND Ixabepilone (BMS-247550), an epothilone B analog, is a microtubule stabilizing agent which has shown activity in several different tumor types and preclinical models in melanoma. In an open label, one-arm, multi-center phase II trial the efficacy and toxicity of this epothilone was investigated in two different cohorts: chemotherapy-naïve (previously untreated) and previously treated...

Journal: :Molecular cancer therapeutics 2003
Lianne Fuino Purva Bali Sylvie Wittmann Sreenivas Donapaty Fei Guo Hirohito Yamaguchi Hong-Gang Wang Peter Atadja Kapil Bhalla

Histone deacetylase inhibitors induce hyperacetylation of the amino-terminal lysine residues of the core nucleosomal histones, which results in chromatin remodeling and altered gene expression. Present studies demonstrate that exposure to a novel hydroxamic acid analogue histone deacetylase inhibitor, LAQ824, induced p21WAF1 and p27KIP1 and caused growth arrest and apoptosis of human breast can...

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