Literature DB >> 18653275

Imatinib resistance in CML.

Gisella Volpe1, Cristina Panuzzo, Stefano Ulisciani, Daniela Cilloni.   

Abstract

Imatinib is, at present, the first-choice treatment for patients with chronic myeloid leukaemia in chronic phase. Despite the impressive rate of complete haematological response and complete cytogenetical remissions, some cases show primary resistance or relapse after an initial response (secondary or acquired resistance). The most common mechanisms responsible for this resistance are BCR/ABL kinase domain mutations, BCR/ABL amplification and over-expression and clonal evolution with activation of additional oncogenic pathways. Here, we describe the molecular basis of imatinib resistance, the significance of molecular monitoring and the current efforts to overcome imatinib resistance, ranging from the development of new drugs to the stimulation of an immune response against the disease.

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Year:  2008        PMID: 18653275     DOI: 10.1016/j.canlet.2008.06.003

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  25 in total

1.  MicroRNAs 130a/b are regulated by BCR-ABL and downregulate expression of CCN3 in CML.

Authors:  Sukanya Suresh; Lynn McCallum; Wanhua Lu; Noureddine Lazar; Bernard Perbal; Alexandra E Irvine
Journal:  J Cell Commun Signal       Date:  2011-06-03       Impact factor: 5.782

2.  Imatinib plasma trough concentration and its correlation with characteristics and response in Chinese CML patients.

Authors:  Qiu-bai Li; Chao Chen; Zhi-chao Chen; Hong-xiang Wang; Yan-lin Wu; Yong You; Ping Zou
Journal:  Acta Pharmacol Sin       Date:  2010-07-19       Impact factor: 6.150

3.  A derivative of epigallocatechin-3-gallate induces apoptosis via SHP-1-mediated suppression of BCR-ABL and STAT3 signalling in chronic myelogenous leukaemia.

Authors:  Ji Hoon Jung; Miyong Yun; Eun-Jeong Choo; Sun-Hee Kim; Myoung-Seok Jeong; Deok-Beom Jung; Hyemin Lee; Eun-Ok Kim; Nobuo Kato; Bonglee Kim; Sanjay K Srivastava; Kunihiro Kaihatsu; Sung-Hoon Kim
Journal:  Br J Pharmacol       Date:  2015-06-04       Impact factor: 8.739

4.  Bcr-abl silencing by specific small-interference RNA expression vector as a potential treatment for chronic myeloid leukemia.

Authors:  Ali Zaree Mahmodabady; Hamid Reza Javadi; Mehdi Kamali; Ali Najafi; Zahra Hojati
Journal:  Iran Biomed J       Date:  2010 Jan-Apr

Review 5.  Kinase inhibitors: the road ahead.

Authors:  Fleur M Ferguson; Nathanael S Gray
Journal:  Nat Rev Drug Discov       Date:  2018-03-16       Impact factor: 84.694

6.  In vivo imaging of Bcr-Abl overexpressing tumors with a radiolabeled imatinib analog as an imaging surrogate for imatinib.

Authors:  Athanasios P Glekas; Nagavara Kishore Pillarsetty; Blesida Punzalan; Nahida Khan; Peter Smith-Jones; Steven M Larson
Journal:  J Nucl Med       Date:  2011-07-15       Impact factor: 10.057

7.  Integrating pharmacogenetics and therapeutic drug monitoring: optimal dosing of imatinib as a case-example.

Authors:  Alain Li-Wan-Po; Peter Farndon; Charles Craddock; Michael Griffiths
Journal:  Eur J Clin Pharmacol       Date:  2010-01-29       Impact factor: 2.953

8.  Anticipating drug resistance in the MAP kinase pathway.

Authors:  Ronen Marmorstein
Journal:  Pigment Cell Melanoma Res       Date:  2009-12-02       Impact factor: 4.693

9.  LQB-118, a pterocarpanquinone structurally related to lapachol [2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone]: a novel class of agent with high apoptotic effect in chronic myeloid leukemia cells.

Authors:  Raquel C Maia; Flavia C Vasconcelos; Thiago de Sá Bacelar; Eduardo J Salustiano; Luis Felipe R da Silva; Débora L Pereira; Arthur Moellman-Coelho; Chaquip D Netto; Alcides J da Silva; Vivian M Rumjanek; Paulo R R Costa
Journal:  Invest New Drugs       Date:  2010-05-25       Impact factor: 3.850

Review 10.  [Molecular tumour therapy].

Authors:  C Michel; A Neubauer; A Burchert
Journal:  Internist (Berl)       Date:  2015-12       Impact factor: 0.743

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