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Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo

[Image: see text] Extracellular acidification indicates a metabolic shift in cancer cells and is, along with tissue hypoxia, a hallmark of tumor malignancy. Thus, non-invasive mapping of extracellular pH (pHe) is essential for researchers to understand the tumor microenvironment and to monitor tumor...

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Autores principales: Nakaoka, Ririko, Kato, Kazuhiro, Yamamoto, Kumiko, Yasui, Hironobu, Matsumoto, Shingo, Kirilyuk, Igor A., Khramtsov, Valery V., Inanami, Osamu, Hirata, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979135/
https://www.ncbi.nlm.nih.gov/pubmed/36725678
http://dx.doi.org/10.1021/acs.analchem.2c03194
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author Nakaoka, Ririko
Kato, Kazuhiro
Yamamoto, Kumiko
Yasui, Hironobu
Matsumoto, Shingo
Kirilyuk, Igor A.
Khramtsov, Valery V.
Inanami, Osamu
Hirata, Hiroshi
author_facet Nakaoka, Ririko
Kato, Kazuhiro
Yamamoto, Kumiko
Yasui, Hironobu
Matsumoto, Shingo
Kirilyuk, Igor A.
Khramtsov, Valery V.
Inanami, Osamu
Hirata, Hiroshi
author_sort Nakaoka, Ririko
collection PubMed
description [Image: see text] Extracellular acidification indicates a metabolic shift in cancer cells and is, along with tissue hypoxia, a hallmark of tumor malignancy. Thus, non-invasive mapping of extracellular pH (pHe) is essential for researchers to understand the tumor microenvironment and to monitor tumor response to metabolism-targeting drugs. While electron paramagnetic resonance (EPR) has been successfully used to map pHe in mouse xenograft models, this method is not sensitive enough to map pHe with a moderate amount of exogenous pH-sensitive probes. Here, we show that a modified EPR system achieves twofold higher sensitivity by using the multiple harmonic detection (MHD) method and improves the robustness of pHe mapping in mouse xenograft models. Our results demonstrate that treatment of a mouse xenograft model of human-derived pancreatic ductal adenocarcinoma cells with the carbonic anhydrase IX (CAIX) inhibitor U-104 delays tumor growth with a concurrent tendency toward further extracellular acidification. We anticipate that EPR-based pHe mapping can be expanded to monitor the response of other metabolism-targeting drugs. Furthermore, pHe monitoring can also be used for the development of improved metabolism-targeting cancer treatments.
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spelling pubmed-99791352023-03-03 Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo Nakaoka, Ririko Kato, Kazuhiro Yamamoto, Kumiko Yasui, Hironobu Matsumoto, Shingo Kirilyuk, Igor A. Khramtsov, Valery V. Inanami, Osamu Hirata, Hiroshi Anal Chem [Image: see text] Extracellular acidification indicates a metabolic shift in cancer cells and is, along with tissue hypoxia, a hallmark of tumor malignancy. Thus, non-invasive mapping of extracellular pH (pHe) is essential for researchers to understand the tumor microenvironment and to monitor tumor response to metabolism-targeting drugs. While electron paramagnetic resonance (EPR) has been successfully used to map pHe in mouse xenograft models, this method is not sensitive enough to map pHe with a moderate amount of exogenous pH-sensitive probes. Here, we show that a modified EPR system achieves twofold higher sensitivity by using the multiple harmonic detection (MHD) method and improves the robustness of pHe mapping in mouse xenograft models. Our results demonstrate that treatment of a mouse xenograft model of human-derived pancreatic ductal adenocarcinoma cells with the carbonic anhydrase IX (CAIX) inhibitor U-104 delays tumor growth with a concurrent tendency toward further extracellular acidification. We anticipate that EPR-based pHe mapping can be expanded to monitor the response of other metabolism-targeting drugs. Furthermore, pHe monitoring can also be used for the development of improved metabolism-targeting cancer treatments. American Chemical Society 2023-02-01 /pmc/articles/PMC9979135/ /pubmed/36725678 http://dx.doi.org/10.1021/acs.analchem.2c03194 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Nakaoka, Ririko
Kato, Kazuhiro
Yamamoto, Kumiko
Yasui, Hironobu
Matsumoto, Shingo
Kirilyuk, Igor A.
Khramtsov, Valery V.
Inanami, Osamu
Hirata, Hiroshi
Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo
title Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo
title_full Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo
title_fullStr Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo
title_full_unstemmed Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo
title_short Electron Paramagnetic Resonance Implemented with Multiple Harmonic Detections Successfully Maps Extracellular pH In Vivo
title_sort electron paramagnetic resonance implemented with multiple harmonic detections successfully maps extracellular ph in vivo
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979135/
https://www.ncbi.nlm.nih.gov/pubmed/36725678
http://dx.doi.org/10.1021/acs.analchem.2c03194
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