Recent advances in methods to assess the activity of the kinome [version 1; referees: 3 approved]

Protein and lipid kinases are deregulated in most, if not all, cancers and are among the most valuable therapeutic targets in these diseases. Despite the introduction of dozens of effective kinase inhibitors into clinical practice, the development of drug resistance remains a major barrier to treatm...

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Main Authors: Maria Radu, Jonathan Chernoff
Format: Article
Language:English
Published: F1000 Research Ltd 2017-06-01
Series:F1000Research
Subjects:
Online Access:https://f1000research.com/articles/6-1004/v1
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spelling doaj-9715b0b15a304368b56ad2e1edc401bc2020-11-25T03:35:34ZengF1000 Research LtdF1000Research2046-14022017-06-01610.12688/f1000research.10962.111816Recent advances in methods to assess the activity of the kinome [version 1; referees: 3 approved]Maria Radu0Jonathan Chernoff1Cancer Biology Program, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA, 19111-2497, USACancer Biology Program, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA, 19111-2497, USAProtein and lipid kinases are deregulated in most, if not all, cancers and are among the most valuable therapeutic targets in these diseases. Despite the introduction of dozens of effective kinase inhibitors into clinical practice, the development of drug resistance remains a major barrier to treatment because of adaption of cellular signaling pathways to bypass targeted kinases. So that the basal and adaptive responses of kinases in cancer can be better understood, new methods have emerged that allow simultaneous and unbiased measurement of the activation state of a substantial fraction of the entire kinome. Here, we discuss such kinome-profiling methodologies, emphasizing the relative strengths and weaknesses of each approach.https://f1000research.com/articles/6-1004/v1BiocatalysisCancer TherapeuticsCell SignalingDrug Discovery & DesignMedical GeneticsProtein Chemistry & Proteomics
collection DOAJ
language English
format Article
sources DOAJ
author Maria Radu
Jonathan Chernoff
spellingShingle Maria Radu
Jonathan Chernoff
Recent advances in methods to assess the activity of the kinome [version 1; referees: 3 approved]
F1000Research
Biocatalysis
Cancer Therapeutics
Cell Signaling
Drug Discovery & Design
Medical Genetics
Protein Chemistry & Proteomics
author_facet Maria Radu
Jonathan Chernoff
author_sort Maria Radu
title Recent advances in methods to assess the activity of the kinome [version 1; referees: 3 approved]
title_short Recent advances in methods to assess the activity of the kinome [version 1; referees: 3 approved]
title_full Recent advances in methods to assess the activity of the kinome [version 1; referees: 3 approved]
title_fullStr Recent advances in methods to assess the activity of the kinome [version 1; referees: 3 approved]
title_full_unstemmed Recent advances in methods to assess the activity of the kinome [version 1; referees: 3 approved]
title_sort recent advances in methods to assess the activity of the kinome [version 1; referees: 3 approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2017-06-01
description Protein and lipid kinases are deregulated in most, if not all, cancers and are among the most valuable therapeutic targets in these diseases. Despite the introduction of dozens of effective kinase inhibitors into clinical practice, the development of drug resistance remains a major barrier to treatment because of adaption of cellular signaling pathways to bypass targeted kinases. So that the basal and adaptive responses of kinases in cancer can be better understood, new methods have emerged that allow simultaneous and unbiased measurement of the activation state of a substantial fraction of the entire kinome. Here, we discuss such kinome-profiling methodologies, emphasizing the relative strengths and weaknesses of each approach.
topic Biocatalysis
Cancer Therapeutics
Cell Signaling
Drug Discovery & Design
Medical Genetics
Protein Chemistry & Proteomics
url https://f1000research.com/articles/6-1004/v1
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