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Imaging of glucose metabolism by 13C-MRI distinguishes pancreatic cancer subtypes in mice
Metabolic differences among and within tumors can be an important determinant in cancer treatment outcome. However, methods for determining these differences non-invasively in vivo is lacking. Using pancreatic ductal adenocarcinoma as a model, we demonstrate that tumor xenografts with a similar gene...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706239/ https://www.ncbi.nlm.nih.gov/pubmed/31408004 http://dx.doi.org/10.7554/eLife.46312 |
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author | Kishimoto, Shun Brender, Jeffrey R Crooks, Daniel R Matsumoto, Shingo Seki, Tomohiro Oshima, Nobu Merkle, Hellmut Lin, Penghui Reed, Galen Chen, Albert P Ardenkjaer-Larsen, Jan Henrik Munasinghe, Jeeva Saito, Keita Yamamoto, Kazutoshi Choyke, Peter L Mitchell, James Lane, Andrew N Fan, Teresa WM Linehan, W Marston Krishna, Murali C |
author_facet | Kishimoto, Shun Brender, Jeffrey R Crooks, Daniel R Matsumoto, Shingo Seki, Tomohiro Oshima, Nobu Merkle, Hellmut Lin, Penghui Reed, Galen Chen, Albert P Ardenkjaer-Larsen, Jan Henrik Munasinghe, Jeeva Saito, Keita Yamamoto, Kazutoshi Choyke, Peter L Mitchell, James Lane, Andrew N Fan, Teresa WM Linehan, W Marston Krishna, Murali C |
author_sort | Kishimoto, Shun |
collection | PubMed |
description | Metabolic differences among and within tumors can be an important determinant in cancer treatment outcome. However, methods for determining these differences non-invasively in vivo is lacking. Using pancreatic ductal adenocarcinoma as a model, we demonstrate that tumor xenografts with a similar genetic background can be distinguished by their differing rates of the metabolism of 13C labeled glucose tracers, which can be imaged without hyperpolarization by using newly developed techniques for noise suppression. Using this method, cancer subtypes that appeared to have similar metabolic profiles based on steady state metabolic measurement can be distinguished from each other. The metabolic maps from 13C-glucose imaging localized lactate production and overall glucose metabolism to different regions of some tumors. Such tumor heterogeneity would not be not detectable in FDG-PET. |
format | Online Article Text |
id | pubmed-6706239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-67062392019-08-26 Imaging of glucose metabolism by 13C-MRI distinguishes pancreatic cancer subtypes in mice Kishimoto, Shun Brender, Jeffrey R Crooks, Daniel R Matsumoto, Shingo Seki, Tomohiro Oshima, Nobu Merkle, Hellmut Lin, Penghui Reed, Galen Chen, Albert P Ardenkjaer-Larsen, Jan Henrik Munasinghe, Jeeva Saito, Keita Yamamoto, Kazutoshi Choyke, Peter L Mitchell, James Lane, Andrew N Fan, Teresa WM Linehan, W Marston Krishna, Murali C eLife Cancer Biology Metabolic differences among and within tumors can be an important determinant in cancer treatment outcome. However, methods for determining these differences non-invasively in vivo is lacking. Using pancreatic ductal adenocarcinoma as a model, we demonstrate that tumor xenografts with a similar genetic background can be distinguished by their differing rates of the metabolism of 13C labeled glucose tracers, which can be imaged without hyperpolarization by using newly developed techniques for noise suppression. Using this method, cancer subtypes that appeared to have similar metabolic profiles based on steady state metabolic measurement can be distinguished from each other. The metabolic maps from 13C-glucose imaging localized lactate production and overall glucose metabolism to different regions of some tumors. Such tumor heterogeneity would not be not detectable in FDG-PET. eLife Sciences Publications, Ltd 2019-08-13 /pmc/articles/PMC6706239/ /pubmed/31408004 http://dx.doi.org/10.7554/eLife.46312 Text en http://creativecommons.org/publicdomain/zero/1.0/ http://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Cancer Biology Kishimoto, Shun Brender, Jeffrey R Crooks, Daniel R Matsumoto, Shingo Seki, Tomohiro Oshima, Nobu Merkle, Hellmut Lin, Penghui Reed, Galen Chen, Albert P Ardenkjaer-Larsen, Jan Henrik Munasinghe, Jeeva Saito, Keita Yamamoto, Kazutoshi Choyke, Peter L Mitchell, James Lane, Andrew N Fan, Teresa WM Linehan, W Marston Krishna, Murali C Imaging of glucose metabolism by 13C-MRI distinguishes pancreatic cancer subtypes in mice |
title | Imaging of glucose metabolism by 13C-MRI distinguishes pancreatic cancer subtypes in mice |
title_full | Imaging of glucose metabolism by 13C-MRI distinguishes pancreatic cancer subtypes in mice |
title_fullStr | Imaging of glucose metabolism by 13C-MRI distinguishes pancreatic cancer subtypes in mice |
title_full_unstemmed | Imaging of glucose metabolism by 13C-MRI distinguishes pancreatic cancer subtypes in mice |
title_short | Imaging of glucose metabolism by 13C-MRI distinguishes pancreatic cancer subtypes in mice |
title_sort | imaging of glucose metabolism by 13c-mri distinguishes pancreatic cancer subtypes in mice |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706239/ https://www.ncbi.nlm.nih.gov/pubmed/31408004 http://dx.doi.org/10.7554/eLife.46312 |
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