نتایج جستجو برای: abl

تعداد نتایج: 7672  

Journal: :Cancer research 2006
John S Tokarski John A Newitt Chieh Ying J Chang Janet D Cheng Michael Wittekind Susan E Kiefer Kevin Kish Francis Y F Lee Robert Borzillerri Louis J Lombardo Dianlin Xie Yaqun Zhang Herbert E Klei

Chronic myeloid leukemia (CML) is caused by the constitutively activated tyrosine kinase breakpoint cluster (BCR)-ABL. Current frontline therapy for CML is imatinib, an inhibitor of BCR-ABL. Although imatinib has a high rate of clinical success in early phase CML, treatment resistance is problematic, particularly in later stages of the disease, and is frequently mediated by mutations in BCR-ABL...

Journal: :Cancer research 2007
Su Chu Liang Li Harjeet Singh Ravi Bhatia

Chronic myelogenous leukemia (CML) results from the transformation of a primitive hematopoietic cell by the BCR/ABL gene. BCR/ABL signaling has been studied in cell lines and murine models, but the transforming effects of BCR/ABL are highly dependent on cellular context, and mechanisms responsible for the transformation of primitive human hematopoietic cells remain poorly understood. Current ta...

Journal: :Blood 2004
Michael G Kharas Jonathan A Deane Stephane Wong Karen R O'Bosky Naomi Rosenberg Owen N Witte David A Fruman

BCR-ABL and v-ABL are oncogenic forms of the Abl tyrosine kinase that can cause leukemias in mice and humans. ABL oncogenes trigger multiple signaling pathways whose contribution to transformation varies among cell types. Activation of phosphoinositide 3-kinase (PI3K) is essential for ABL-dependent proliferation and survival in some cell types, and global PI3K inhibitors can enhance the antileu...

2017
Yinghui Sun Na Zhao Huan Wang Qiong Wu Yunqi Han Qichao Liu Mangang Wu Yuliang Liu Fansheng Kong He Wang Ying Sun Deguang Sun Lutao Jing Guojing Tang Yuandong Hu Dengming Xiao Hong Luo Yongxin Han Yong Peng

Kinase inhibitors that target Bcr-Abl are highly effective in the treatment of chronic myeloid leukemia (CML). However, these inhibitors are often invalidated due to the drug resistance. Therefore, the discovery and development of novel Bcr-Abl inhibitors is required to overwhelm the drug resistance in the treatment of CML resistant to the currently used first-line Bcr-Abl inhibitors. Herein we...

2011
Thomas O’Hare Michael W.N. Deininger Christopher A. Eide Tim Clackson Brian J. Druker

Beginning with imatinib a decade ago, therapy based on targeted inhibition of the BCR-ABL kinase has greatly improved the prognosis for chronic myeloid leukemia (CML) patients. The recognition that some patients experience relapse due to resistance-conferring point mutations within BCR-ABL sparked the development of the second-generation ABL kinase inhibitors nilotinib and dasatinib. Collective...

2016
Fabienne Lamballe Sara Toscano Filippo Conti Maria Arechederra Nathalie Baeza Dominique Figarella-Branger Françoise Helmbacher Flavio Maina

The cytoplasmic tyrosine kinase ABL exerts positive or negative effects in solid tumours according to the cellular context, thus functioning as a "switch modulator". The therapeutic effects of drugs targeting a set of signals encompassing ABL have been explored in several solid tumours. However, the net contribution of ABL inhibition by these agents remains elusive as these drugs also act on ot...

Journal: :Cancer research 2001
R Nimmanapalli E O'Bryan K Bhalla

HL-60/Bcr-Abl cells, with ectopic expression of p185 Bcr-Abl tyrosine kinase (TK), and K562 cells, with endogenous expression of p210 Bcr-Abl TK, display a high degree of resistance against antileukemic drug-induced apoptosis (G. Fang et al., Blood, 96: 2246-2256, 2000). Present studies demonstrate that treatment with ansamycin antibiotic geldanamycin (GA), or its less toxic analogue 17-allylam...

Journal: :international journal of hematology-oncology and stem cell research 0
fatemeh nadali pathology department, school of medicine, isfahan university of medical sciences, isfahan, iran sh ferdowsi school of allied health sciences, tehran university of medical sciences, tehran, iran p karimzadeh school of allied health sciences, tehran university of medical sciences, tehran, iran bahram chahardouli hematology-oncology and bmt research center, shariati hospital, tehran university of medical science, tehran, iran n einollahi school of allied health sciences, tehran university of medical sciences, tehran, iran sa mousavi hematology-oncology and bmt research center, shariati hospital, tehran university of medical science, tehran, iran

jak2 is a tyrosine kinase that plays an important role in the signaling pathways of many hematopoietic growth factor receptors. a single acquired point mutation – v617f – in jak2 occurs in the great majority of patients with polycythemia vera (pv) and approximately half of the patients with idiopathic myelofibrosis (imf) or essential thrombocythemia (et). in contrast, the jak2-v617f mutation is...

2016
Silvia Bono Matteo Lulli Vito Giuseppe D'Agostino Federico Di Gesualdo Rosa Loffredo Maria Grazia Cipolleschi Alessandro Provenzani Elisabetta Rovida Persio Dello Sbarba

BCR/Abl protein drives the onset and progression of Chronic Myeloid Leukemia (CML). We previously showed that BCR/Abl protein is suppressed in low oxygen, where viable cells retain stem cell potential. This study addressed the regulation of BCR/Abl protein expression under oxygen or glucose shortage, characteristic of the in vivo environment where cells resistant to tyrosine kinase inhibitors (...

Journal: :Journal of controlled release : official journal of the Controlled Release Society 2009
Andrew S Dixon Mudit Kakar Korbinian M H Schneider Jonathan E Constance Blake C Paullin Carol S Lim

Altering the subcellular localization of signal transducing proteins is a novel approach for therapeutic intervention. Mislocalization of tumor suppressors, oncogenes, or factors involved in apoptosis results in aberrant functioning of these proteins, leading to disease. In the case of chronic myelogenous leukemia (CML), cytoplasmic Bcr-Abl causes oncogenesis/proliferation. On the other hand, n...

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