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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
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.
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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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