Literature DB >> 15778081

FLT-3: a new focus in the understanding of acute leukemia.

Ana Markovic1, Karen L MacKenzie, Richard B Lock.   

Abstract

The FMS-like tyrosine kinase-3 (FLT-3), which belongs to the class III receptor tyrosine kinase family, is primarily expressed by hematopoietic cells and plays an important role in hematopoiesis. FLT-3 is also expressed in the majority of acute leukemias, in which the presence of FLT-3 activating mutations is associated with poor prognosis. Consequently, there has been a recent surge in the development of FLT-3 inhibitors for the molecular targeting of leukemia, and many of these are now in clinical trials. An improved understanding of how FLT-3 interacts with its ligand, as well as how FLT-3 activating mutations are able to trigger downstream intracellular signaling pathways, will provide greater insight to how small molecule inhibitors may best be utilized and combined with established chemotherapeutic drugs for the management of patients with high-risk acute leukemia.

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Year:  2005        PMID: 15778081     DOI: 10.1016/j.biocel.2004.12.005

Source DB:  PubMed          Journal:  Int J Biochem Cell Biol        ISSN: 1357-2725            Impact factor:   5.085


  26 in total

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Authors:  James A McCubrey; Linda S Steelman; Richard A Franklin; Steven L Abrams; William H Chappell; Ellis W T Wong; Brian D Lehmann; David M Terrian; Jorg Basecke; Franca Stivala; Massimo Libra; Camilla Evangelisti; Alberto M Martelli
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Review 4.  Targeting FLT3 to treat leukemia.

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Journal:  Expert Opin Ther Targets       Date:  2014-09-18       Impact factor: 6.902

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Authors:  Jason M Duran; Catherine A Makarewich; Danielle Trappanese; Polina Gross; Sharmeen Husain; Jonathan Dunn; Hind Lal; Thomas E Sharp; Timothy Starosta; Ronald J Vagnozzi; Remus M Berretta; Mary Barbe; Daohai Yu; Erhe Gao; Hajime Kubo; Thomas Force; Steven R Houser
Journal:  Circ Res       Date:  2014-04-09       Impact factor: 17.367

6.  FLT-3 expression and function on microglia in multiple sclerosis.

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Journal:  Exp Mol Pathol       Date:  2010-05-31       Impact factor: 3.362

Review 7.  Targeting PI3K/AKT/mTOR network for treatment of leukemia.

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Journal:  Cell Mol Life Sci       Date:  2015-02-25       Impact factor: 9.261

8.  Cells expressing FLT3/ITD mutations exhibit elevated repair errors generated through alternative NHEJ pathways: implications for genomic instability and therapy.

Authors:  Jinshui Fan; Li Li; Donald Small; Feyruz Rassool
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Review 9.  Combination of antiangiogenesis with chemotherapy for more effective cancer treatment.

Authors:  Jie Ma; David J Waxman
Journal:  Mol Cancer Ther       Date:  2008-12       Impact factor: 6.261

10.  Discovery of a highly potent FLT3 kinase inhibitor for FLT3-ITD-positive AML.

Authors:  H Wu; A Wang; Z Qi; X Li; C Chen; K Yu; F Zou; C Hu; W Wang; Z Zhao; J Wu; J Liu; X Liu; L Wang; W Wang; S Zhang; R M Stone; I A Galinsky; J D Griffin; D Weinstock; A Christodoulou; H Wang; Y Shen; Z Zhai; E L Weisberg; J Liu; Q Liu
Journal:  Leukemia       Date:  2016-05-25       Impact factor: 11.528

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