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Molecular imaging: what can be used today: Monday 3 October 2005, 11:15–12:00
Biochemical cellular targets and more general metabolic processes in cancer cells can be visualised. Extensive data are available on molecular imaging in preclinical models. However, innovative tracers move slowly to the clinic. This review provides information on the currently available methods of...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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e-MED
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1665304/ https://www.ncbi.nlm.nih.gov/pubmed/16361133 http://dx.doi.org/10.1102/1470-7330.2005.0023 |
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author | Jager, P L de Korte, M A Lub-de Hooge, M N van Waarde, A Koopmans, K P Perik, P J de Vries, E G E |
author_facet | Jager, P L de Korte, M A Lub-de Hooge, M N van Waarde, A Koopmans, K P Perik, P J de Vries, E G E |
author_sort | Jager, P L |
collection | PubMed |
description | Biochemical cellular targets and more general metabolic processes in cancer cells can be visualised. Extensive data are available on molecular imaging in preclinical models. However, innovative tracers move slowly to the clinic. This review provides information on the currently available methods of metabolic imaging, especially using PET in humans. The uptake mechanisms of tracer methods and a brief discussion of the more ‘molecular’ targeted methods are presented. The main focus is on the different classes of tracers and their application in various types of cancer within each class of tracers, based on the current literature and our own experience. Studies with [(18)F]FDG (energy metabolism), radiolabelled amino acids (protein metabolism), [(18)F]FLT (DNA metabolism), [(11)C]choline (cell membrane metabolism) as general metabolic tracer methods and [(18)F]DOPA (biogenic amine metabolism) as a more specific tracer method are discussed. As an example, molecular imaging methods that target the HER2 receptor and somatostatin receptor are described. |
format | Text |
id | pubmed-1665304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | e-MED |
record_format | MEDLINE/PubMed |
spelling | pubmed-16653042006-12-14 Molecular imaging: what can be used today: Monday 3 October 2005, 11:15–12:00 Jager, P L de Korte, M A Lub-de Hooge, M N van Waarde, A Koopmans, K P Perik, P J de Vries, E G E Cancer Imaging Keynote Lecture Biochemical cellular targets and more general metabolic processes in cancer cells can be visualised. Extensive data are available on molecular imaging in preclinical models. However, innovative tracers move slowly to the clinic. This review provides information on the currently available methods of metabolic imaging, especially using PET in humans. The uptake mechanisms of tracer methods and a brief discussion of the more ‘molecular’ targeted methods are presented. The main focus is on the different classes of tracers and their application in various types of cancer within each class of tracers, based on the current literature and our own experience. Studies with [(18)F]FDG (energy metabolism), radiolabelled amino acids (protein metabolism), [(18)F]FLT (DNA metabolism), [(11)C]choline (cell membrane metabolism) as general metabolic tracer methods and [(18)F]DOPA (biogenic amine metabolism) as a more specific tracer method are discussed. As an example, molecular imaging methods that target the HER2 receptor and somatostatin receptor are described. e-MED 2005-11-23 /pmc/articles/PMC1665304/ /pubmed/16361133 http://dx.doi.org/10.1102/1470-7330.2005.0023 Text en Copyright © 2005 International Cancer Imaging Society |
spellingShingle | Keynote Lecture Jager, P L de Korte, M A Lub-de Hooge, M N van Waarde, A Koopmans, K P Perik, P J de Vries, E G E Molecular imaging: what can be used today: Monday 3 October 2005, 11:15–12:00 |
title | Molecular imaging: what can be used today: Monday 3 October 2005, 11:15–12:00 |
title_full | Molecular imaging: what can be used today: Monday 3 October 2005, 11:15–12:00 |
title_fullStr | Molecular imaging: what can be used today: Monday 3 October 2005, 11:15–12:00 |
title_full_unstemmed | Molecular imaging: what can be used today: Monday 3 October 2005, 11:15–12:00 |
title_short | Molecular imaging: what can be used today: Monday 3 October 2005, 11:15–12:00 |
title_sort | molecular imaging: what can be used today: monday 3 october 2005, 11:15–12:00 |
topic | Keynote Lecture |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1665304/ https://www.ncbi.nlm.nih.gov/pubmed/16361133 http://dx.doi.org/10.1102/1470-7330.2005.0023 |
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