Literature DB >> 15710324

AMN107: tightening the grip of imatinib.

Thomas O'Hare1, Denise K Walters, Michael W N Deininger, Brian J Druker.   

Abstract

The Abl inhibitor imatinib is a highly effective therapy for patients with chronic myeloid leukemia. Relapses are relatively uncommon in newly diagnosed patients, but are the rule in patients with more advanced disease. Mutations in the BCR-ABL gene are the most common cause of relapse. Working from the imatinib chemical structure, a higher-affinity family member, AMN107, was designed. AMN107 is approximately 20-fold more potent than imatinib, and this translates into improved inhibitory activity against most of the common BCR-ABL mutations. The implications of these results, and the potential role this and other novel ABL inhibitors may have in treating patients with CML, are discussed.

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Year:  2005        PMID: 15710324     DOI: 10.1016/j.ccr.2005.01.020

Source DB:  PubMed          Journal:  Cancer Cell        ISSN: 1535-6108            Impact factor:   31.743


  23 in total

Review 1.  [Basics of molecular diagnostics and therapy of malignant tumors].

Authors:  P T Daniel; B Dörken
Journal:  Internist (Berl)       Date:  2005-08       Impact factor: 0.743

2.  Development of 'DFG-out' inhibitors of gatekeeper mutant kinases.

Authors:  Hwan Geun Choi; Jianming Zhang; Ellen Weisberg; James D Griffin; Taebo Sim; Nathanael S Gray
Journal:  Bioorg Med Chem Lett       Date:  2012-06-23       Impact factor: 2.823

Review 3.  Selecting the best frontline treatment in chronic myeloid leukemia.

Authors:  Musa Yilmaz; Yasmin Abaza; Elias Jabbour
Journal:  Curr Hematol Malig Rep       Date:  2015-06       Impact factor: 3.952

4.  Broad spectrum alkynyl inhibitors of T315I Bcr-Abl.

Authors:  Xianming Deng; Sang Min Lim; Jianming Zhang; Nathanael S Gray
Journal:  Bioorg Med Chem Lett       Date:  2010-05-19       Impact factor: 2.823

5.  The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes.

Authors:  David P Steensma; Gordon W Dewald; Terra L Lasho; Heather L Powell; Rebecca F McClure; Ross L Levine; D Gary Gilliland; Ayalew Tefferi
Journal:  Blood       Date:  2005-04-28       Impact factor: 22.113

6.  A type-II kinase inhibitor capable of inhibiting the T315I "gatekeeper" mutant of Bcr-Abl.

Authors:  Hwan Geun Choi; Pingda Ren; Francisco Adrian; Fangxian Sun; Hyun Soo Lee; Xia Wang; Qiang Ding; Guobao Zhang; Yongping Xie; Jianming Zhang; Yi Liu; Tove Tuntland; Markus Warmuth; Paul W Manley; Jürgen Mestan; Nathanael S Gray; Taebo Sim
Journal:  J Med Chem       Date:  2010-08-12       Impact factor: 7.446

7.  Nilotinib for the treatment of chronic myeloid leukemia: An evidence-based review.

Authors:  Elias Jabbour; Jorge Cortes; Hagop Kantarjian
Journal:  Core Evid       Date:  2010-06-15

8.  Targeting autophagy augments the anticancer activity of the histone deacetylase inhibitor SAHA to overcome Bcr-Abl-mediated drug resistance.

Authors:  Jennifer S Carew; Steffan T Nawrocki; Charissa N Kahue; Hui Zhang; Chunying Yang; Linda Chung; Janet A Houghton; Peng Huang; Francis J Giles; John L Cleveland
Journal:  Blood       Date:  2007-03-15       Impact factor: 22.113

9.  Productive replication of Ebola virus is regulated by the c-Abl1 tyrosine kinase.

Authors:  Mayra García; Arik Cooper; Wei Shi; William Bornmann; Ricardo Carrion; Daniel Kalman; Gary J Nabel
Journal:  Sci Transl Med       Date:  2012-02-29       Impact factor: 17.956

10.  Suppression of programmed cell death 4 (PDCD4) protein expression by BCR-ABL-regulated engagement of the mTOR/p70 S6 kinase pathway.

Authors:  Nathalie Carayol; Efstratios Katsoulidis; Antonella Sassano; Jessica K Altman; Brian J Druker; Leonidas C Platanias
Journal:  J Biol Chem       Date:  2008-01-26       Impact factor: 5.157

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