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(18)F-FIMP: a LAT1-specific PET probe for discrimination between tumor tissue and inflammation

Positron emission tomography (PET) imaging can assist in the early-phase diagnostic and therapeutic evaluation of tumors. Here, we report the radiosynthesis, small animal PET imaging, and biological evaluation of a L-type amino acid transporter 1 (LAT1)-specific PET probe, (18)F-FIMP. This probe dem...

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Autores principales: Nozaki, Satoshi, Nakatani, Yuka, Mawatari, Aya, Shibata, Nina, Hume, William E., Hayashinaka, Emi, Wada, Yasuhiro, Doi, Hisashi, Watanabe, Yasuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823354/
https://www.ncbi.nlm.nih.gov/pubmed/31673030
http://dx.doi.org/10.1038/s41598-019-52270-x
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author Nozaki, Satoshi
Nakatani, Yuka
Mawatari, Aya
Shibata, Nina
Hume, William E.
Hayashinaka, Emi
Wada, Yasuhiro
Doi, Hisashi
Watanabe, Yasuyoshi
author_facet Nozaki, Satoshi
Nakatani, Yuka
Mawatari, Aya
Shibata, Nina
Hume, William E.
Hayashinaka, Emi
Wada, Yasuhiro
Doi, Hisashi
Watanabe, Yasuyoshi
author_sort Nozaki, Satoshi
collection PubMed
description Positron emission tomography (PET) imaging can assist in the early-phase diagnostic and therapeutic evaluation of tumors. Here, we report the radiosynthesis, small animal PET imaging, and biological evaluation of a L-type amino acid transporter 1 (LAT1)-specific PET probe, (18)F-FIMP. This probe demonstrates increased tumor specificity, compared to existing tumor-specific PET probes ((18)F-FET, (11)C-MET, and (18)F-FDG). Evaluation of probes by in vivo PET imaging, (18)F-FIMP showed intense accumulation in LAT1-positive tumor tissues, but not in inflamed lesions, whereas intense accumulation of (18)F-FDG was observed in both tumor tissues and in inflamed lesions. Metabolite analysis showed that (18)F-FIMP was stable in liver microsomes, and mice tissues (plasma, urine, liver, pancreas, and tumor). Investigation of the protein incorporation of (18)F-FIMP showed that it was not incorporated into protein. Furthermore, the expected mean absorbed dose of (18)F-FIMP in humans was comparable or slightly higher than that of (18)F-FDG and indicated that (18)F-FIMP may be a safe PET probe for use in humans. (18)F-FIMP may provide improved specificity for tumor diagnosis, compared to (18)F-FDG, (18)F-FET, and (11)C-MET. This probe may be suitable for PET imaging for glioblastoma and the early-phase monitoring of cancer therapy outcomes.
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spelling pubmed-68233542019-11-12 (18)F-FIMP: a LAT1-specific PET probe for discrimination between tumor tissue and inflammation Nozaki, Satoshi Nakatani, Yuka Mawatari, Aya Shibata, Nina Hume, William E. Hayashinaka, Emi Wada, Yasuhiro Doi, Hisashi Watanabe, Yasuyoshi Sci Rep Article Positron emission tomography (PET) imaging can assist in the early-phase diagnostic and therapeutic evaluation of tumors. Here, we report the radiosynthesis, small animal PET imaging, and biological evaluation of a L-type amino acid transporter 1 (LAT1)-specific PET probe, (18)F-FIMP. This probe demonstrates increased tumor specificity, compared to existing tumor-specific PET probes ((18)F-FET, (11)C-MET, and (18)F-FDG). Evaluation of probes by in vivo PET imaging, (18)F-FIMP showed intense accumulation in LAT1-positive tumor tissues, but not in inflamed lesions, whereas intense accumulation of (18)F-FDG was observed in both tumor tissues and in inflamed lesions. Metabolite analysis showed that (18)F-FIMP was stable in liver microsomes, and mice tissues (plasma, urine, liver, pancreas, and tumor). Investigation of the protein incorporation of (18)F-FIMP showed that it was not incorporated into protein. Furthermore, the expected mean absorbed dose of (18)F-FIMP in humans was comparable or slightly higher than that of (18)F-FDG and indicated that (18)F-FIMP may be a safe PET probe for use in humans. (18)F-FIMP may provide improved specificity for tumor diagnosis, compared to (18)F-FDG, (18)F-FET, and (11)C-MET. This probe may be suitable for PET imaging for glioblastoma and the early-phase monitoring of cancer therapy outcomes. Nature Publishing Group UK 2019-10-31 /pmc/articles/PMC6823354/ /pubmed/31673030 http://dx.doi.org/10.1038/s41598-019-52270-x Text en © The Author(s) 2019 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 Article
Nozaki, Satoshi
Nakatani, Yuka
Mawatari, Aya
Shibata, Nina
Hume, William E.
Hayashinaka, Emi
Wada, Yasuhiro
Doi, Hisashi
Watanabe, Yasuyoshi
(18)F-FIMP: a LAT1-specific PET probe for discrimination between tumor tissue and inflammation
title (18)F-FIMP: a LAT1-specific PET probe for discrimination between tumor tissue and inflammation
title_full (18)F-FIMP: a LAT1-specific PET probe for discrimination between tumor tissue and inflammation
title_fullStr (18)F-FIMP: a LAT1-specific PET probe for discrimination between tumor tissue and inflammation
title_full_unstemmed (18)F-FIMP: a LAT1-specific PET probe for discrimination between tumor tissue and inflammation
title_short (18)F-FIMP: a LAT1-specific PET probe for discrimination between tumor tissue and inflammation
title_sort (18)f-fimp: a lat1-specific pet probe for discrimination between tumor tissue and inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823354/
https://www.ncbi.nlm.nih.gov/pubmed/31673030
http://dx.doi.org/10.1038/s41598-019-52270-x
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