Literature DB >> 19104514

Targeting cancer with small molecule kinase inhibitors.

Jianming Zhang1, Priscilla L Yang, Nathanael S Gray.   

Abstract

Deregulation of kinase activity has emerged as a major mechanism by which cancer cells evade normal physiological constraints on growth and survival. To date, 11 kinase inhibitors have received US Food and Drug Administration approval as cancer treatments, and there are considerable efforts to develop selective small molecule inhibitors for a host of other kinases that are implicated in cancer and other diseases. Herein we discuss the current challenges in the field, such as designing selective inhibitors and developing strategies to overcome resistance mutations. This Review provides a broad overview of some of the approaches currently used to discover and characterize new kinase inhibitors.

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Year:  2009        PMID: 19104514     DOI: 10.1038/nrc2559

Source DB:  PubMed          Journal:  Nat Rev Cancer        ISSN: 1474-175X            Impact factor:   60.716


  105 in total

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Review 3.  Ba/F3 cells and their use in kinase drug discovery.

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Review 4.  The Eleventh Datta Lecture. The structural basis for substrate recognition and control by protein kinases.

Authors:  L N Johnson; E D Lowe; M E Noble; D J Owen
Journal:  FEBS Lett       Date:  1998-06-23       Impact factor: 4.124

Review 5.  Current development of mTOR inhibitors as anticancer agents.

Authors:  Sandrine Faivre; Guido Kroemer; Eric Raymond
Journal:  Nat Rev Drug Discov       Date:  2006-08       Impact factor: 84.694

6.  The small-molecule inhibitor BI 2536 reveals novel insights into mitotic roles of polo-like kinase 1.

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Journal:  Curr Biol       Date:  2007-02-08       Impact factor: 10.834

7.  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
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8.  Selectivity-determining residues in Plk1.

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9.  Structural basis for the autoinhibition of c-Abl tyrosine kinase.

Authors:  Bhushan Nagar; Oliver Hantschel; Matthew A Young; Klaus Scheffzek; Darren Veach; William Bornmann; Bayard Clarkson; Giulio Superti-Furga; John Kuriyan
Journal:  Cell       Date:  2003-03-21       Impact factor: 41.582

10.  BMS-214662 potently induces apoptosis of chronic myeloid leukemia stem and progenitor cells and synergizes with tyrosine kinase inhibitors.

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  805 in total

1.  A Chemoproteomic Strategy for Direct and Proteome-Wide Covalent Inhibitor Target-Site Identification.

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Review 4.  SCF ubiquitin ligase-targeted therapies.

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Review 5.  Sunitinib, hypertension, and heart failure: a model for kinase inhibitor-mediated cardiotoxicity.

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6.  Direct Substrate Identification with an Analog Sensitive (AS) Viral Cyclin-Dependent Kinase (v-Cdk).

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7.  Modularly Constructed Synthetic Granzyme B Molecule Enables Interrogation of Intracellular Proteases for Targeted Cytotoxicity.

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Journal:  ACS Synth Biol       Date:  2017-05-22       Impact factor: 5.110

8.  Discovery and Structure-Activity Relationship Study of (Z)-5-Methylenethiazolidin-4-one Derivatives as Potent and Selective Pan-phosphatidylinositol 5-Phosphate 4-Kinase Inhibitors.

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9.  Low Concentration Microenvironments Enhance the Migration of Neonatal Cells of Glial Lineage.

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10.  Kinome chemoproteomics characterization of pyrrolo[3,4-c]pyrazoles as potent and selective inhibitors of glycogen synthase kinase 3.

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Journal:  Mol Omics       Date:  2018-02-12
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