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Development of [(18)F]ICMT-11 for Imaging Caspase-3/7 Activity during Therapy-Induced Apoptosis
Insufficient apoptosis is a recognised hallmark of cancer. A strategy to quantitatively measure apoptosis in vivo would be of immense value in both drug discovery and routine patient management. The first irreversible step in the apoptosis cascade is activation of the “executioner” caspase-3 enzyme...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465189/ https://www.ncbi.nlm.nih.gov/pubmed/32781531 http://dx.doi.org/10.3390/cancers12082191 |
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author | García-Argüello, Segundo Francisco Lopez-Lorenzo, Beatriz Cornelissen, Bart Smith, Graham |
author_facet | García-Argüello, Segundo Francisco Lopez-Lorenzo, Beatriz Cornelissen, Bart Smith, Graham |
author_sort | García-Argüello, Segundo Francisco |
collection | PubMed |
description | Insufficient apoptosis is a recognised hallmark of cancer. A strategy to quantitatively measure apoptosis in vivo would be of immense value in both drug discovery and routine patient management. The first irreversible step in the apoptosis cascade is activation of the “executioner” caspase-3 enzyme to commence cleavage of key structural proteins. One strategy to measure caspase-3 activity is Positron Emission Tomography using isatin-5-sulfonamide radiotracers. One such radiotracer is [(18)F]ICMT-11, which has progressed to clinical application. This review summarises the design and development process for [(18)F]ICMT-11, suggesting potential avenues for further innovation. |
format | Online Article Text |
id | pubmed-7465189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74651892020-09-04 Development of [(18)F]ICMT-11 for Imaging Caspase-3/7 Activity during Therapy-Induced Apoptosis García-Argüello, Segundo Francisco Lopez-Lorenzo, Beatriz Cornelissen, Bart Smith, Graham Cancers (Basel) Review Insufficient apoptosis is a recognised hallmark of cancer. A strategy to quantitatively measure apoptosis in vivo would be of immense value in both drug discovery and routine patient management. The first irreversible step in the apoptosis cascade is activation of the “executioner” caspase-3 enzyme to commence cleavage of key structural proteins. One strategy to measure caspase-3 activity is Positron Emission Tomography using isatin-5-sulfonamide radiotracers. One such radiotracer is [(18)F]ICMT-11, which has progressed to clinical application. This review summarises the design and development process for [(18)F]ICMT-11, suggesting potential avenues for further innovation. MDPI 2020-08-06 /pmc/articles/PMC7465189/ /pubmed/32781531 http://dx.doi.org/10.3390/cancers12082191 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review García-Argüello, Segundo Francisco Lopez-Lorenzo, Beatriz Cornelissen, Bart Smith, Graham Development of [(18)F]ICMT-11 for Imaging Caspase-3/7 Activity during Therapy-Induced Apoptosis |
title | Development of [(18)F]ICMT-11 for Imaging Caspase-3/7 Activity during Therapy-Induced Apoptosis |
title_full | Development of [(18)F]ICMT-11 for Imaging Caspase-3/7 Activity during Therapy-Induced Apoptosis |
title_fullStr | Development of [(18)F]ICMT-11 for Imaging Caspase-3/7 Activity during Therapy-Induced Apoptosis |
title_full_unstemmed | Development of [(18)F]ICMT-11 for Imaging Caspase-3/7 Activity during Therapy-Induced Apoptosis |
title_short | Development of [(18)F]ICMT-11 for Imaging Caspase-3/7 Activity during Therapy-Induced Apoptosis |
title_sort | development of [(18)f]icmt-11 for imaging caspase-3/7 activity during therapy-induced apoptosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465189/ https://www.ncbi.nlm.nih.gov/pubmed/32781531 http://dx.doi.org/10.3390/cancers12082191 |
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