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(99m)Tc-radiolabeled GE11-modified peptide for ovarian tumor targeting

BACKGROUND: Ovarian cancer is a serious threat for women health and the early diagnosis of this cancer might improves the survival rate of patients. The use of the targeted radiopharmaceuticals could be a non-invasive and logical method for tumor imaging. The aim of this study was to radiolabel GE11...

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Autores principales: Rahmanian, Najmeh, Hosseinimehr, Seyed Jalal, Khalaj, Ali, Noaparast, Zohreh, Abedi, Seyed Mohammad, Sabzevari, Omid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414288/
https://www.ncbi.nlm.nih.gov/pubmed/28464952
http://dx.doi.org/10.1186/s40199-017-0179-8
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author Rahmanian, Najmeh
Hosseinimehr, Seyed Jalal
Khalaj, Ali
Noaparast, Zohreh
Abedi, Seyed Mohammad
Sabzevari, Omid
author_facet Rahmanian, Najmeh
Hosseinimehr, Seyed Jalal
Khalaj, Ali
Noaparast, Zohreh
Abedi, Seyed Mohammad
Sabzevari, Omid
author_sort Rahmanian, Najmeh
collection PubMed
description BACKGROUND: Ovarian cancer is a serious threat for women health and the early diagnosis of this cancer might improves the survival rate of patients. The use of the targeted radiopharmaceuticals could be a non-invasive and logical method for tumor imaging. The aim of this study was to radiolabel GE11 peptide as a new specific probe for imaging of ovarian tumor. METHODS: HYNIC-SSS-GE11 peptide was labeled with (99m)Tc using tricine as a coligand. The (99m)Tc-tricine-HYNIC-SSS-GE11 peptide was evaluated for specific cellular binding in three cell lines with different levels of EGFR expression. Tumor targeting was assessed in SKOV3 tumor bearing mice. RESULTS: By using tricine as a coligand, labeling yield was more than 98% and the stability of the radiolabelled peptide in human serum up to 4 h was 96%. The in vitro cell uptake test showed that this radiolabeled peptide had a good affinity to SKOV3 cells with dissociation constant of 73 nM. The in vivo results showed a tumor/muscle ratio of 3.2 at 4 h following injection of (99m)Tc-tricine-HYNIC-SSS-GE11 peptide. CONCLUSIONS: Results of this study showed that (99m)Tc-tricine-HYNIC-SSS-GE11 peptide could be a promising tool for diagnosis and staging of ovarian cancer. GRAPHICAL ABSTRACT: (99m)Tc-tricine-HYNIC-SSS-GE11, a novl targeted agent for ovarian tumor imaging [Image: see text]
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spelling pubmed-54142882017-05-03 (99m)Tc-radiolabeled GE11-modified peptide for ovarian tumor targeting Rahmanian, Najmeh Hosseinimehr, Seyed Jalal Khalaj, Ali Noaparast, Zohreh Abedi, Seyed Mohammad Sabzevari, Omid Daru Research Article BACKGROUND: Ovarian cancer is a serious threat for women health and the early diagnosis of this cancer might improves the survival rate of patients. The use of the targeted radiopharmaceuticals could be a non-invasive and logical method for tumor imaging. The aim of this study was to radiolabel GE11 peptide as a new specific probe for imaging of ovarian tumor. METHODS: HYNIC-SSS-GE11 peptide was labeled with (99m)Tc using tricine as a coligand. The (99m)Tc-tricine-HYNIC-SSS-GE11 peptide was evaluated for specific cellular binding in three cell lines with different levels of EGFR expression. Tumor targeting was assessed in SKOV3 tumor bearing mice. RESULTS: By using tricine as a coligand, labeling yield was more than 98% and the stability of the radiolabelled peptide in human serum up to 4 h was 96%. The in vitro cell uptake test showed that this radiolabeled peptide had a good affinity to SKOV3 cells with dissociation constant of 73 nM. The in vivo results showed a tumor/muscle ratio of 3.2 at 4 h following injection of (99m)Tc-tricine-HYNIC-SSS-GE11 peptide. CONCLUSIONS: Results of this study showed that (99m)Tc-tricine-HYNIC-SSS-GE11 peptide could be a promising tool for diagnosis and staging of ovarian cancer. GRAPHICAL ABSTRACT: (99m)Tc-tricine-HYNIC-SSS-GE11, a novl targeted agent for ovarian tumor imaging [Image: see text] BioMed Central 2017-05-02 /pmc/articles/PMC5414288/ /pubmed/28464952 http://dx.doi.org/10.1186/s40199-017-0179-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Rahmanian, Najmeh
Hosseinimehr, Seyed Jalal
Khalaj, Ali
Noaparast, Zohreh
Abedi, Seyed Mohammad
Sabzevari, Omid
(99m)Tc-radiolabeled GE11-modified peptide for ovarian tumor targeting
title (99m)Tc-radiolabeled GE11-modified peptide for ovarian tumor targeting
title_full (99m)Tc-radiolabeled GE11-modified peptide for ovarian tumor targeting
title_fullStr (99m)Tc-radiolabeled GE11-modified peptide for ovarian tumor targeting
title_full_unstemmed (99m)Tc-radiolabeled GE11-modified peptide for ovarian tumor targeting
title_short (99m)Tc-radiolabeled GE11-modified peptide for ovarian tumor targeting
title_sort (99m)tc-radiolabeled ge11-modified peptide for ovarian tumor targeting
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414288/
https://www.ncbi.nlm.nih.gov/pubmed/28464952
http://dx.doi.org/10.1186/s40199-017-0179-8
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