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DCE-MRI of Tumor Hypoxia and Hypoxia-Associated Aggressiveness
Tumor hypoxia is associated with resistance to treatment, aggressive growth, metastatic dissemination, and poor clinical outcome in many cancer types. The potential of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) to assess the extent of hypoxia in tumors has been investigated in se...
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/PMC7409330/ https://www.ncbi.nlm.nih.gov/pubmed/32698525 http://dx.doi.org/10.3390/cancers12071979 |
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author | Gaustad, Jon-Vidar Hauge, Anette Wegner, Catherine S. Simonsen, Trude G. Lund, Kjersti V. Hansem, Lise Mari K. Rofstad, Einar K. |
author_facet | Gaustad, Jon-Vidar Hauge, Anette Wegner, Catherine S. Simonsen, Trude G. Lund, Kjersti V. Hansem, Lise Mari K. Rofstad, Einar K. |
author_sort | Gaustad, Jon-Vidar |
collection | PubMed |
description | Tumor hypoxia is associated with resistance to treatment, aggressive growth, metastatic dissemination, and poor clinical outcome in many cancer types. The potential of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) to assess the extent of hypoxia in tumors has been investigated in several studies in our laboratory. Cervical carcinoma, melanoma, and pancreatic ductal adenocarcinoma (PDAC) xenografts have been used as models of human cancer, and the transfer rate constant (K(trans)) and the extravascular extracellular volume fraction (v(e)) have been derived from DCE-MRI data by using Tofts standard pharmacokinetic model and a population-based arterial input function. K(trans) was found to reflect naturally occurring and treatment-induced hypoxia when hypoxia was caused by low blood perfusion, radiation responsiveness when radiation resistance was due to hypoxia, and metastatic potential when metastasis was hypoxia-induced. K(trans) was also associated with outcome for patients with locally-advanced cervical carcinoma treated with cisplatin-based chemoradiotherapy. Together, the studies imply that DCE-MRI can provide valuable information on the hypoxic status of cervical carcinoma, melanoma, and PDAC. In this communication, we review and discuss the studies and provide some recommendations as to how DCE-MRI data can be analyzed and interpreted to assess tumor hypoxia. |
format | Online Article Text |
id | pubmed-7409330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74093302020-08-25 DCE-MRI of Tumor Hypoxia and Hypoxia-Associated Aggressiveness Gaustad, Jon-Vidar Hauge, Anette Wegner, Catherine S. Simonsen, Trude G. Lund, Kjersti V. Hansem, Lise Mari K. Rofstad, Einar K. Cancers (Basel) Review Tumor hypoxia is associated with resistance to treatment, aggressive growth, metastatic dissemination, and poor clinical outcome in many cancer types. The potential of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) to assess the extent of hypoxia in tumors has been investigated in several studies in our laboratory. Cervical carcinoma, melanoma, and pancreatic ductal adenocarcinoma (PDAC) xenografts have been used as models of human cancer, and the transfer rate constant (K(trans)) and the extravascular extracellular volume fraction (v(e)) have been derived from DCE-MRI data by using Tofts standard pharmacokinetic model and a population-based arterial input function. K(trans) was found to reflect naturally occurring and treatment-induced hypoxia when hypoxia was caused by low blood perfusion, radiation responsiveness when radiation resistance was due to hypoxia, and metastatic potential when metastasis was hypoxia-induced. K(trans) was also associated with outcome for patients with locally-advanced cervical carcinoma treated with cisplatin-based chemoradiotherapy. Together, the studies imply that DCE-MRI can provide valuable information on the hypoxic status of cervical carcinoma, melanoma, and PDAC. In this communication, we review and discuss the studies and provide some recommendations as to how DCE-MRI data can be analyzed and interpreted to assess tumor hypoxia. MDPI 2020-07-20 /pmc/articles/PMC7409330/ /pubmed/32698525 http://dx.doi.org/10.3390/cancers12071979 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 Gaustad, Jon-Vidar Hauge, Anette Wegner, Catherine S. Simonsen, Trude G. Lund, Kjersti V. Hansem, Lise Mari K. Rofstad, Einar K. DCE-MRI of Tumor Hypoxia and Hypoxia-Associated Aggressiveness |
title | DCE-MRI of Tumor Hypoxia and Hypoxia-Associated Aggressiveness |
title_full | DCE-MRI of Tumor Hypoxia and Hypoxia-Associated Aggressiveness |
title_fullStr | DCE-MRI of Tumor Hypoxia and Hypoxia-Associated Aggressiveness |
title_full_unstemmed | DCE-MRI of Tumor Hypoxia and Hypoxia-Associated Aggressiveness |
title_short | DCE-MRI of Tumor Hypoxia and Hypoxia-Associated Aggressiveness |
title_sort | dce-mri of tumor hypoxia and hypoxia-associated aggressiveness |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409330/ https://www.ncbi.nlm.nih.gov/pubmed/32698525 http://dx.doi.org/10.3390/cancers12071979 |
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