Literature DB >> 21235428

Mechanisms of drug resistance in kinases.

Rina Barouch-Bentov1, Karsten Sauer.   

Abstract

INTRODUCTION: because of their important roles in disease and excellent 'druggability', kinases have become the second largest drug target family. The great success of the BCR-ABL inhibitor imatinib in treating chronic myelogenous leukemia illustrates the high potential of kinase inhibitor (KI) therapeutics, but also unveils a major limitation: the development of drug resistance. This is a significant concern as KIs reach large patient populations for an expanding array of indications. AREAS COVERED: we provide an up-to-date understanding of the mechanisms through which KIs function and through which cells can become KI-resistant. We review current and future approaches to overcome KI resistance, focusing on currently approved KIs and KIs in clinical trials. We then discuss approaches to improve KI efficacy and overcome drug resistance and novel approaches to develop less drug resistance-prone KI therapeutics. EXPERT OPINION: although drug resistance is a concern for current KI therapeutics, recent progress in our understanding of the underlying mechanisms and promising technological advances may overcome this limitation and provide powerful new therapeutics.

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Year:  2011        PMID: 21235428      PMCID: PMC3095104          DOI: 10.1517/13543784.2011.546344

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  145 in total

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Journal:  Cell       Date:  2002-05-03       Impact factor: 41.582

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Journal:  J Med Chem       Date:  2009-07-09       Impact factor: 7.446

Review 3.  The road less traveled: modulating signal transduction enzymes by inhibiting their protein-protein interactions.

Authors:  Michelle R Arkin; Adrian Whitty
Journal:  Curr Opin Chem Biol       Date:  2009-06-22       Impact factor: 8.822

Review 4.  Cell cycle kinases as therapeutic targets for cancer.

Authors:  Silvia Lapenna; Antonio Giordano
Journal:  Nat Rev Drug Discov       Date:  2009-07       Impact factor: 84.694

5.  Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification.

Authors:  M E Gorre; M Mohammed; K Ellwood; N Hsu; R Paquette; P N Rao; C L Sawyers
Journal:  Science       Date:  2001-06-21       Impact factor: 47.728

6.  Crystal structure of a transition state mimic of the catalytic subunit of cAMP-dependent protein kinase.

Authors:  Pearl Akamine; Nguyen-Huu Xuong; Susan S Taylor
Journal:  Nat Struct Biol       Date:  2002-04

7.  Autoinhibition of c-Abl.

Authors:  Helma Pluk; Karel Dorey; Giulio Superti-Furga
Journal:  Cell       Date:  2002-01-25       Impact factor: 41.582

8.  Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia.

Authors:  Neil P Shah; John M Nicoll; Bhushan Nagar; Mercedes E Gorre; Ronald L Paquette; John Kuriyan; Charles L Sawyers
Journal:  Cancer Cell       Date:  2002-08       Impact factor: 31.743

9.  Clinical resistance to the kinase inhibitor STI-571 in chronic myeloid leukemia by mutation of Tyr-253 in the Abl kinase domain P-loop.

Authors:  Sergei Roumiantsev; Neil P Shah; Mercedes E Gorre; John Nicoll; Bradley B Brasher; Charles L Sawyers; Richard A Van Etten
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-29       Impact factor: 11.205

10.  Crystal structures of the kinase domain of c-Abl in complex with the small molecule inhibitors PD173955 and imatinib (STI-571).

Authors:  Bhushan Nagar; William G Bornmann; Patricia Pellicena; Thomas Schindler; Darren R Veach; W Todd Miller; Bayard Clarkson; John Kuriyan
Journal:  Cancer Res       Date:  2002-08-01       Impact factor: 12.701

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  60 in total

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Journal:  Bioorg Med Chem Lett       Date:  2012-06-06       Impact factor: 2.823

2.  Novel iodoacetamido benzoheterocyclic derivatives with potent antileukemic activity are inhibitors of STAT5 phosphorylation.

Authors:  Romeo Romagnoli; Pier Giovanni Baraldi; Filippo Prencipe; Carlota Lopez-Cara; Riccardo Rondanin; Daniele Simoni; Ernest Hamel; Stefania Grimaudo; Rosaria Maria Pipitone; Maria Meli; Manlio Tolomeo
Journal:  Eur J Med Chem       Date:  2015-11-27       Impact factor: 6.514

3.  Cumulative mechanism of several major imatinib-resistant mutations in Abl kinase.

Authors:  Marc Hoemberger; Warintra Pitsawong; Dorothee Kern
Journal:  Proc Natl Acad Sci U S A       Date:  2020-07-27       Impact factor: 11.205

4.  Two-state dynamics of the SH3-SH2 tandem of Abl kinase and the allosteric role of the N-cap.

Authors:  Carles Corbi-Verge; Fabrizio Marinelli; Ana Zafra-Ruano; Javier Ruiz-Sanz; Irene Luque; José D Faraldo-Gómez
Journal:  Proc Natl Acad Sci U S A       Date:  2013-08-19       Impact factor: 11.205

5.  Leveraging Atropisomerism to Obtain a Selective Inhibitor of RET Kinase with Secondary Activities toward EGFR Mutants.

Authors:  Sean T Toenjes; Valeria Garcia; Sean M Maddox; Gregory A Dawson; Maria A Ortiz; F Javier Piedrafita; Jeffrey L Gustafson
Journal:  ACS Chem Biol       Date:  2019-08-29       Impact factor: 5.100

6.  Transcriptomic silencing as a potential mechanism of treatment resistance.

Authors:  Jacob J Adashek; Shumei Kato; Rahul Parulkar; Christopher W Szeto; J Zachary Sanborn; Charles J Vaske; Stephen C Benz; Sandeep K Reddy; Razelle Kurzrock
Journal:  JCI Insight       Date:  2020-06-04

Review 7.  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

8.  Understanding inhibitor resistance in Mps1 kinase through novel biophysical assays and structures.

Authors:  Yoshitaka Hiruma; Andre Koch; Nazila Hazraty; Foteini Tsakou; René H Medema; Robbie P Joosten; Anastassis Perrakis
Journal:  J Biol Chem       Date:  2017-07-18       Impact factor: 5.157

Review 9.  Acquired Resistance to Drugs Targeting Tyrosine Kinases.

Authors:  Steven A Rosenzweig
Journal:  Adv Cancer Res       Date:  2018-03-02       Impact factor: 6.242

10.  Dual inhibition of allosteric mitogen-activated protein kinase (MEK) and phosphatidylinositol 3-kinase (PI3K) oncogenic targets with a bifunctional inhibitor.

Authors:  Marcian E Van Dort; Stefanie Galbán; Hanxiao Wang; Judith Sebolt-Leopold; Christopher Whitehead; Hao Hong; Alnawaz Rehemtulla; Brian D Ross
Journal:  Bioorg Med Chem       Date:  2015-03-06       Impact factor: 3.641

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