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The use of hyperpolarised (13)C-MRI in clinical body imaging to probe cancer metabolism
Metabolic reprogramming is one of the hallmarks of cancer and includes the Warburg effect, which is exhibited by many tumours. This can be exploited by positron emission tomography (PET) as part of routine clinical cancer imaging. However, an emerging and alternative method to detect altered metabol...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007617/ https://www.ncbi.nlm.nih.gov/pubmed/33504974 http://dx.doi.org/10.1038/s41416-020-01224-6 |
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author | Woitek, Ramona Gallagher, Ferdia A. |
author_facet | Woitek, Ramona Gallagher, Ferdia A. |
author_sort | Woitek, Ramona |
collection | PubMed |
description | Metabolic reprogramming is one of the hallmarks of cancer and includes the Warburg effect, which is exhibited by many tumours. This can be exploited by positron emission tomography (PET) as part of routine clinical cancer imaging. However, an emerging and alternative method to detect altered metabolism is carbon-13 magnetic resonance imaging (MRI) following injection of hyperpolarised [1-(13)C]pyruvate. The technique increases the signal-to-noise ratio for the detection of hyperpolarised (13)C-labelled metabolites by several orders of magnitude and facilitates the dynamic, noninvasive imaging of the exchange of (13)C-pyruvate to (13)C-lactate over time. The method has produced promising preclinical results in the area of oncology and is currently being explored in human imaging studies. The first translational studies have demonstrated the safety and feasibility of the technique in patients with prostate, renal, breast and pancreatic cancer, as well as revealing a successful response to treatment in breast and prostate cancer patients at an earlier stage than multiparametric MRI. This review will focus on the strengths of the technique and its applications in the area of oncological body MRI including noninvasive characterisation of disease aggressiveness, mapping of tumour heterogeneity, and early response assessment. A comparison of hyperpolarised (13)C-MRI with state-of-the-art multiparametric MRI is likely to reveal the unique additional information and applications offered by the technique. |
format | Online Article Text |
id | pubmed-8007617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80076172021-04-16 The use of hyperpolarised (13)C-MRI in clinical body imaging to probe cancer metabolism Woitek, Ramona Gallagher, Ferdia A. Br J Cancer Review Article Metabolic reprogramming is one of the hallmarks of cancer and includes the Warburg effect, which is exhibited by many tumours. This can be exploited by positron emission tomography (PET) as part of routine clinical cancer imaging. However, an emerging and alternative method to detect altered metabolism is carbon-13 magnetic resonance imaging (MRI) following injection of hyperpolarised [1-(13)C]pyruvate. The technique increases the signal-to-noise ratio for the detection of hyperpolarised (13)C-labelled metabolites by several orders of magnitude and facilitates the dynamic, noninvasive imaging of the exchange of (13)C-pyruvate to (13)C-lactate over time. The method has produced promising preclinical results in the area of oncology and is currently being explored in human imaging studies. The first translational studies have demonstrated the safety and feasibility of the technique in patients with prostate, renal, breast and pancreatic cancer, as well as revealing a successful response to treatment in breast and prostate cancer patients at an earlier stage than multiparametric MRI. This review will focus on the strengths of the technique and its applications in the area of oncological body MRI including noninvasive characterisation of disease aggressiveness, mapping of tumour heterogeneity, and early response assessment. A comparison of hyperpolarised (13)C-MRI with state-of-the-art multiparametric MRI is likely to reveal the unique additional information and applications offered by the technique. Nature Publishing Group UK 2021-01-28 2021-03-30 /pmc/articles/PMC8007617/ /pubmed/33504974 http://dx.doi.org/10.1038/s41416-020-01224-6 Text en © The Author(s) 2021 Open Access 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 http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Article Woitek, Ramona Gallagher, Ferdia A. The use of hyperpolarised (13)C-MRI in clinical body imaging to probe cancer metabolism |
title | The use of hyperpolarised (13)C-MRI in clinical body imaging to probe cancer metabolism |
title_full | The use of hyperpolarised (13)C-MRI in clinical body imaging to probe cancer metabolism |
title_fullStr | The use of hyperpolarised (13)C-MRI in clinical body imaging to probe cancer metabolism |
title_full_unstemmed | The use of hyperpolarised (13)C-MRI in clinical body imaging to probe cancer metabolism |
title_short | The use of hyperpolarised (13)C-MRI in clinical body imaging to probe cancer metabolism |
title_sort | use of hyperpolarised (13)c-mri in clinical body imaging to probe cancer metabolism |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007617/ https://www.ncbi.nlm.nih.gov/pubmed/33504974 http://dx.doi.org/10.1038/s41416-020-01224-6 |
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