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Biomarkers of apoptosis

Within the era of molecularly targeted anticancer agents, it has become increasingly important to provide proof of mechanism as early on as possible in the drug development cycle, especially in the clinic. Selective activation of apoptosis is often cited as one of the major goals of cancer chemother...

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Autores principales: Ward, T H, Cummings, J, Dean, E, Greystoke, A, Hou, J M, Backen, A, Ranson, M, Dive, C
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2538762/
https://www.ncbi.nlm.nih.gov/pubmed/19238626
http://dx.doi.org/10.1038/sj.bjc.6604519
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author Ward, T H
Cummings, J
Dean, E
Greystoke, A
Hou, J M
Backen, A
Ranson, M
Dive, C
author_facet Ward, T H
Cummings, J
Dean, E
Greystoke, A
Hou, J M
Backen, A
Ranson, M
Dive, C
author_sort Ward, T H
collection PubMed
description Within the era of molecularly targeted anticancer agents, it has become increasingly important to provide proof of mechanism as early on as possible in the drug development cycle, especially in the clinic. Selective activation of apoptosis is often cited as one of the major goals of cancer chemotherapy. Thus, the present minireview focuses on a discussion of the pros and cons of a variety of methodological approaches to detect different components of the apoptotic cascade as potential biomarkers of programmed cell death. The bulk of the discussion centres on serological assays utilising the technique of ELISA, since here there is an obvious advantage of sampling multiple time points. Potential biomarkers of apoptosis including circulating tumour cells, cytokeratins and DNA nucleosomes are discussed at length. However, accepting that a single biomarker may not have the power to predict proof of concept and patient outcome, it is clear that in the future more emphasis will be placed on technologies that can analyse panels of biomarkers in small volumes of samples. To this end the increased throughput afforded by multiplex ELISA technologies is discussed.
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spelling pubmed-25387622009-09-16 Biomarkers of apoptosis Ward, T H Cummings, J Dean, E Greystoke, A Hou, J M Backen, A Ranson, M Dive, C Br J Cancer Minireview Within the era of molecularly targeted anticancer agents, it has become increasingly important to provide proof of mechanism as early on as possible in the drug development cycle, especially in the clinic. Selective activation of apoptosis is often cited as one of the major goals of cancer chemotherapy. Thus, the present minireview focuses on a discussion of the pros and cons of a variety of methodological approaches to detect different components of the apoptotic cascade as potential biomarkers of programmed cell death. The bulk of the discussion centres on serological assays utilising the technique of ELISA, since here there is an obvious advantage of sampling multiple time points. Potential biomarkers of apoptosis including circulating tumour cells, cytokeratins and DNA nucleosomes are discussed at length. However, accepting that a single biomarker may not have the power to predict proof of concept and patient outcome, it is clear that in the future more emphasis will be placed on technologies that can analyse panels of biomarkers in small volumes of samples. To this end the increased throughput afforded by multiplex ELISA technologies is discussed. Nature Publishing Group 2008-09-16 2008-08-26 /pmc/articles/PMC2538762/ /pubmed/19238626 http://dx.doi.org/10.1038/sj.bjc.6604519 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Minireview
Ward, T H
Cummings, J
Dean, E
Greystoke, A
Hou, J M
Backen, A
Ranson, M
Dive, C
Biomarkers of apoptosis
title Biomarkers of apoptosis
title_full Biomarkers of apoptosis
title_fullStr Biomarkers of apoptosis
title_full_unstemmed Biomarkers of apoptosis
title_short Biomarkers of apoptosis
title_sort biomarkers of apoptosis
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2538762/
https://www.ncbi.nlm.nih.gov/pubmed/19238626
http://dx.doi.org/10.1038/sj.bjc.6604519
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