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PET Metabolic Biomarkers for Cancer

The body’s main fuel sources are fats, carbohydrates (glucose), proteins, and ketone bodies. It is well known that an important hallmark of cancer cells is the overconsumption of glucose. Positron emission tomography (PET) imaging using the glucose analog (18)F-fluorodeoxyglucose ((18)F-FDG) has bee...

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Detalles Bibliográficos
Autores principales: Croteau, Etienne, Renaud, Jennifer M., Richard, Marie Anne, Ruddy, Terrence D., Bénard, François, deKemp, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030827/
https://www.ncbi.nlm.nih.gov/pubmed/27679534
http://dx.doi.org/10.4137/BIC.S27483
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author Croteau, Etienne
Renaud, Jennifer M.
Richard, Marie Anne
Ruddy, Terrence D.
Bénard, François
deKemp, Robert A.
author_facet Croteau, Etienne
Renaud, Jennifer M.
Richard, Marie Anne
Ruddy, Terrence D.
Bénard, François
deKemp, Robert A.
author_sort Croteau, Etienne
collection PubMed
description The body’s main fuel sources are fats, carbohydrates (glucose), proteins, and ketone bodies. It is well known that an important hallmark of cancer cells is the overconsumption of glucose. Positron emission tomography (PET) imaging using the glucose analog (18)F-fluorodeoxyglucose ((18)F-FDG) has been a powerful cancer diagnostic tool for many decades. Apart from surgery, chemotherapy and radiotherapy represent the two main domains for cancer therapy, targeting tumor proliferation, cell division, and DNA replication—all processes that require a large amount of energy. Currently, in vivo clinical imaging of metabolism is performed almost exclusively using PET radiotracers that assess oxygen consumption and mechanisms of energy substrate consumption. This paper reviews the utility of PET imaging biomarkers for the detection of cancer proliferation, vascularization, metabolism, treatment response, and follow-up after radiation therapy, chemotherapy, and chemotherapy-related side effects.
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spelling pubmed-50308272016-09-27 PET Metabolic Biomarkers for Cancer Croteau, Etienne Renaud, Jennifer M. Richard, Marie Anne Ruddy, Terrence D. Bénard, François deKemp, Robert A. Biomark Cancer Review The body’s main fuel sources are fats, carbohydrates (glucose), proteins, and ketone bodies. It is well known that an important hallmark of cancer cells is the overconsumption of glucose. Positron emission tomography (PET) imaging using the glucose analog (18)F-fluorodeoxyglucose ((18)F-FDG) has been a powerful cancer diagnostic tool for many decades. Apart from surgery, chemotherapy and radiotherapy represent the two main domains for cancer therapy, targeting tumor proliferation, cell division, and DNA replication—all processes that require a large amount of energy. Currently, in vivo clinical imaging of metabolism is performed almost exclusively using PET radiotracers that assess oxygen consumption and mechanisms of energy substrate consumption. This paper reviews the utility of PET imaging biomarkers for the detection of cancer proliferation, vascularization, metabolism, treatment response, and follow-up after radiation therapy, chemotherapy, and chemotherapy-related side effects. Libertas Academica 2016-09-20 /pmc/articles/PMC5030827/ /pubmed/27679534 http://dx.doi.org/10.4137/BIC.S27483 Text en © 2016 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 license.
spellingShingle Review
Croteau, Etienne
Renaud, Jennifer M.
Richard, Marie Anne
Ruddy, Terrence D.
Bénard, François
deKemp, Robert A.
PET Metabolic Biomarkers for Cancer
title PET Metabolic Biomarkers for Cancer
title_full PET Metabolic Biomarkers for Cancer
title_fullStr PET Metabolic Biomarkers for Cancer
title_full_unstemmed PET Metabolic Biomarkers for Cancer
title_short PET Metabolic Biomarkers for Cancer
title_sort pet metabolic biomarkers for cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030827/
https://www.ncbi.nlm.nih.gov/pubmed/27679534
http://dx.doi.org/10.4137/BIC.S27483
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