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Evaluation of [(99m)Tc][Tc-HYNIC/EDDA]-Tyr as a target for metabolic tumor imaging in B16F10 melanoma tumor

OBJECTIVE(S): Clinical interest in metabolic imaging of cancer has been growing in recent years. The increase in protein metabolism of cancer cells is interesting target for metabolic tumor imaging, for which radiolabeled amino acids can be applied. The aim of this study was to evaluate a newly deve...

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Autores principales: Yaghoubi Mogadam, Hemat, Erfani, Mostafa, Nikpassand, Mohammad, Mokhtary, Masoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205849/
https://www.ncbi.nlm.nih.gov/pubmed/35800424
http://dx.doi.org/10.22038/AOJNMB.2021.60334.1420
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author Yaghoubi Mogadam, Hemat
Erfani, Mostafa
Nikpassand, Mohammad
Mokhtary, Masoud
author_facet Yaghoubi Mogadam, Hemat
Erfani, Mostafa
Nikpassand, Mohammad
Mokhtary, Masoud
author_sort Yaghoubi Mogadam, Hemat
collection PubMed
description OBJECTIVE(S): Clinical interest in metabolic imaging of cancer has been growing in recent years. The increase in protein metabolism of cancer cells is interesting target for metabolic tumor imaging, for which radiolabeled amino acids can be applied. The aim of this study was to evaluate a newly developed radiolabeled amino acid as an imaging protein metabolism in melanoma tumor. METHODS: The radiolabeled tyrosine ([(99m)Tc][Tc-HYNIC/EDDA]-Tyr) was prepared and its biological properties was evaluated in B16F10 melanoma tumor. Moreover organs uptake and tumor accumulation were measured in mouse bearing B16F10 melanoma tumor. RESULTS: Radiolabeled tyrosine was attached in B16F10 melanoma cells and showed the cell binding capacity of 13.82±0.73%. In animal study, the accumulation of radiolabeled tyrosine was observed in B16F10 melanoma tumor (2.15±0.09 %ID/g) after 30 min post injection, so that the uptake ratio of tumor to muscle was about 5.11. Through scintigraphy process the melanoma tumor clearly visualized in mice at 30 min post injection. CONCLUSION: These data suggest that the novel radiotracer ([(99m)Tc][Tc-HYNIC/EDDA]-Tyr) as an protein metabolism imaging agent, is able to transfer into melanoma cells and show great expectation for the clinical application in the imaging of melanoma tumors.
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spelling pubmed-92058492022-07-06 Evaluation of [(99m)Tc][Tc-HYNIC/EDDA]-Tyr as a target for metabolic tumor imaging in B16F10 melanoma tumor Yaghoubi Mogadam, Hemat Erfani, Mostafa Nikpassand, Mohammad Mokhtary, Masoud Asia Ocean J Nucl Med Biol Original Article OBJECTIVE(S): Clinical interest in metabolic imaging of cancer has been growing in recent years. The increase in protein metabolism of cancer cells is interesting target for metabolic tumor imaging, for which radiolabeled amino acids can be applied. The aim of this study was to evaluate a newly developed radiolabeled amino acid as an imaging protein metabolism in melanoma tumor. METHODS: The radiolabeled tyrosine ([(99m)Tc][Tc-HYNIC/EDDA]-Tyr) was prepared and its biological properties was evaluated in B16F10 melanoma tumor. Moreover organs uptake and tumor accumulation were measured in mouse bearing B16F10 melanoma tumor. RESULTS: Radiolabeled tyrosine was attached in B16F10 melanoma cells and showed the cell binding capacity of 13.82±0.73%. In animal study, the accumulation of radiolabeled tyrosine was observed in B16F10 melanoma tumor (2.15±0.09 %ID/g) after 30 min post injection, so that the uptake ratio of tumor to muscle was about 5.11. Through scintigraphy process the melanoma tumor clearly visualized in mice at 30 min post injection. CONCLUSION: These data suggest that the novel radiotracer ([(99m)Tc][Tc-HYNIC/EDDA]-Tyr) as an protein metabolism imaging agent, is able to transfer into melanoma cells and show great expectation for the clinical application in the imaging of melanoma tumors. Mashhad University of Medical Sciences 2022 /pmc/articles/PMC9205849/ /pubmed/35800424 http://dx.doi.org/10.22038/AOJNMB.2021.60334.1420 Text en © 2022 mums.ac.ir All rights reserved https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yaghoubi Mogadam, Hemat
Erfani, Mostafa
Nikpassand, Mohammad
Mokhtary, Masoud
Evaluation of [(99m)Tc][Tc-HYNIC/EDDA]-Tyr as a target for metabolic tumor imaging in B16F10 melanoma tumor
title Evaluation of [(99m)Tc][Tc-HYNIC/EDDA]-Tyr as a target for metabolic tumor imaging in B16F10 melanoma tumor
title_full Evaluation of [(99m)Tc][Tc-HYNIC/EDDA]-Tyr as a target for metabolic tumor imaging in B16F10 melanoma tumor
title_fullStr Evaluation of [(99m)Tc][Tc-HYNIC/EDDA]-Tyr as a target for metabolic tumor imaging in B16F10 melanoma tumor
title_full_unstemmed Evaluation of [(99m)Tc][Tc-HYNIC/EDDA]-Tyr as a target for metabolic tumor imaging in B16F10 melanoma tumor
title_short Evaluation of [(99m)Tc][Tc-HYNIC/EDDA]-Tyr as a target for metabolic tumor imaging in B16F10 melanoma tumor
title_sort evaluation of [(99m)tc][tc-hynic/edda]-tyr as a target for metabolic tumor imaging in b16f10 melanoma tumor
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205849/
https://www.ncbi.nlm.nih.gov/pubmed/35800424
http://dx.doi.org/10.22038/AOJNMB.2021.60334.1420
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