Literature DB >> 24910388

Drug resistance to targeted therapies: déjà vu all over again.

Floris H Groenendijk1, René Bernards2.   

Abstract

A major limitation of targeted anticancer therapies is intrinsic or acquired resistance. This review emphasizes similarities in the mechanisms of resistance to endocrine therapies in breast cancer and those seen with the new generation of targeted cancer therapeutics. Resistance to single-agent cancer therapeutics is frequently the result of reactivation of the signaling pathway, indicating that a major limitation of targeted agents lies in their inability to fully block the cancer-relevant signaling pathway. The development of mechanism-based combinations of targeted therapies together with non-invasive molecular disease monitoring is a logical way forward to delay and ultimately overcome drug resistance development.
Copyright © 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Anticancer therapy; Drug combinations; Drug resistance; Endocrine therapy; Pathway reactivation; Targeted therapy

Mesh:

Substances:

Year:  2014        PMID: 24910388      PMCID: PMC5528618          DOI: 10.1016/j.molonc.2014.05.004

Source DB:  PubMed          Journal:  Mol Oncol        ISSN: 1574-7891            Impact factor:   6.603


  126 in total

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Journal:  Breast Cancer Res Treat       Date:  2010-08-22       Impact factor: 4.872

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Review 7.  Drug resistance to targeted therapies: déjà vu all over again.

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