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Pharmacodynamic Biomarker Development for PI3K Pathway Therapeutics

The phosphatidylinositol 3-kinase (PI3K) signaling pathway is integral to many essential cell processes, including cell growth, differentiation, proliferation, motility, and metabolism. Somatic mutations and genetic amplifications that result in activation of the pathway are frequently detected in c...

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Detalles Bibliográficos
Autores principales: Josephs, Debra H., Sarker, Debashis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762492/
https://www.ncbi.nlm.nih.gov/pubmed/26917948
http://dx.doi.org/10.4137/TOG.S30529
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author Josephs, Debra H.
Sarker, Debashis
author_facet Josephs, Debra H.
Sarker, Debashis
author_sort Josephs, Debra H.
collection PubMed
description The phosphatidylinositol 3-kinase (PI3K) signaling pathway is integral to many essential cell processes, including cell growth, differentiation, proliferation, motility, and metabolism. Somatic mutations and genetic amplifications that result in activation of the pathway are frequently detected in cancer. This has led to the development of rationally designed therapeutics targeting key members of the pathway. Critical to the successful development of these drugs are pharmacodynamic biomarkers that aim to define the degree of target and pathway inhibition. In this review, we discuss the pharmacodynamic biomarkers that have been utilized in early-phase clinical trials of PI3K pathway inhibitors. We focus on the challenges related to development and interpretation of these assays, their optimal integration with pharmacokinetic and predictive biomarkers, and future strategies to ensure successful development of PI3K pathway inhibitors within a personalized medicine paradigm for cancer.
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spelling pubmed-47624922016-02-25 Pharmacodynamic Biomarker Development for PI3K Pathway Therapeutics Josephs, Debra H. Sarker, Debashis Transl Oncogenomics Review The phosphatidylinositol 3-kinase (PI3K) signaling pathway is integral to many essential cell processes, including cell growth, differentiation, proliferation, motility, and metabolism. Somatic mutations and genetic amplifications that result in activation of the pathway are frequently detected in cancer. This has led to the development of rationally designed therapeutics targeting key members of the pathway. Critical to the successful development of these drugs are pharmacodynamic biomarkers that aim to define the degree of target and pathway inhibition. In this review, we discuss the pharmacodynamic biomarkers that have been utilized in early-phase clinical trials of PI3K pathway inhibitors. We focus on the challenges related to development and interpretation of these assays, their optimal integration with pharmacokinetic and predictive biomarkers, and future strategies to ensure successful development of PI3K pathway inhibitors within a personalized medicine paradigm for cancer. Libertas Academica 2016-02-21 /pmc/articles/PMC4762492/ /pubmed/26917948 http://dx.doi.org/10.4137/TOG.S30529 Text en © 2015 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article published under the Creative Commons CC-BY-NC 3.0 license.
spellingShingle Review
Josephs, Debra H.
Sarker, Debashis
Pharmacodynamic Biomarker Development for PI3K Pathway Therapeutics
title Pharmacodynamic Biomarker Development for PI3K Pathway Therapeutics
title_full Pharmacodynamic Biomarker Development for PI3K Pathway Therapeutics
title_fullStr Pharmacodynamic Biomarker Development for PI3K Pathway Therapeutics
title_full_unstemmed Pharmacodynamic Biomarker Development for PI3K Pathway Therapeutics
title_short Pharmacodynamic Biomarker Development for PI3K Pathway Therapeutics
title_sort pharmacodynamic biomarker development for pi3k pathway therapeutics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4762492/
https://www.ncbi.nlm.nih.gov/pubmed/26917948
http://dx.doi.org/10.4137/TOG.S30529
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