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PET imaging of tumour hypoxia
Tumour hypoxia represents a significant challenge to the curability of human tumours leading to treatment resistance and enhanced tumour progression. Tumour hypoxia can be detected by non-invasive and invasive techniques but the inter-relationships between these remains largely undefined. [(18)F]Flu...
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Formato: | Texto |
Lenguaje: | English |
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e-MED
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1805075/ https://www.ncbi.nlm.nih.gov/pubmed/17114063 http://dx.doi.org/10.1102/1470-7330.2006.9018 |
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author | Padhani, Anwar |
author_facet | Padhani, Anwar |
author_sort | Padhani, Anwar |
collection | PubMed |
description | Tumour hypoxia represents a significant challenge to the curability of human tumours leading to treatment resistance and enhanced tumour progression. Tumour hypoxia can be detected by non-invasive and invasive techniques but the inter-relationships between these remains largely undefined. [(18)F]Fluoromisonidazole-3-fluoro-1-(2 (′)-nitro-1 (′)-imidazolyl)-2-propanol ([(18)F]MISO) and Cu-diacetyl-bis(N(4)-methylthiosemicarbazone (Cu-ATSM)-positron emission tomography (PET), and blood oxygen level-dependent (BOLD)-magnetic resonance imaging (MRI) are the lead contenders for human application based on their non-invasive nature, ease of use and robustness, measurement of hypoxia status, validity, ability to demonstrate heterogeneity and general availability; PET techniques are the primary focus of this review. |
format | Text |
id | pubmed-1805075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | e-MED |
record_format | MEDLINE/PubMed |
spelling | pubmed-18050752008-10-31 PET imaging of tumour hypoxia Padhani, Anwar Cancer Imaging Article Tumour hypoxia represents a significant challenge to the curability of human tumours leading to treatment resistance and enhanced tumour progression. Tumour hypoxia can be detected by non-invasive and invasive techniques but the inter-relationships between these remains largely undefined. [(18)F]Fluoromisonidazole-3-fluoro-1-(2 (′)-nitro-1 (′)-imidazolyl)-2-propanol ([(18)F]MISO) and Cu-diacetyl-bis(N(4)-methylthiosemicarbazone (Cu-ATSM)-positron emission tomography (PET), and blood oxygen level-dependent (BOLD)-magnetic resonance imaging (MRI) are the lead contenders for human application based on their non-invasive nature, ease of use and robustness, measurement of hypoxia status, validity, ability to demonstrate heterogeneity and general availability; PET techniques are the primary focus of this review. e-MED 2006-10-31 /pmc/articles/PMC1805075/ /pubmed/17114063 http://dx.doi.org/10.1102/1470-7330.2006.9018 Text en Copyright © 2006 International Cancer Imaging Society |
spellingShingle | Article Padhani, Anwar PET imaging of tumour hypoxia |
title | PET imaging of tumour hypoxia |
title_full | PET imaging of tumour hypoxia |
title_fullStr | PET imaging of tumour hypoxia |
title_full_unstemmed | PET imaging of tumour hypoxia |
title_short | PET imaging of tumour hypoxia |
title_sort | pet imaging of tumour hypoxia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1805075/ https://www.ncbi.nlm.nih.gov/pubmed/17114063 http://dx.doi.org/10.1102/1470-7330.2006.9018 |
work_keys_str_mv | AT padhanianwar petimagingoftumourhypoxia |