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Molecular Imaging of Chemokine Receptor CXCR4

CXCR4 was found to be expressed by many different types of human cancers and its expression has been correlated with tumor aggressiveness, poor prognosis and resistance to chemotherapy. CXCR4 was also shown to contribute to metastatic seeding of organs that express its ligand CXCL12 and support the...

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Autores principales: Weiss, Ido. D., Jacobson, Orit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563082/
https://www.ncbi.nlm.nih.gov/pubmed/23382787
http://dx.doi.org/10.7150/thno.4835
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author Weiss, Ido. D.
Jacobson, Orit
author_facet Weiss, Ido. D.
Jacobson, Orit
author_sort Weiss, Ido. D.
collection PubMed
description CXCR4 was found to be expressed by many different types of human cancers and its expression has been correlated with tumor aggressiveness, poor prognosis and resistance to chemotherapy. CXCR4 was also shown to contribute to metastatic seeding of organs that express its ligand CXCL12 and support the survival of these cells. These findings suggest that CXCR4 is a potentially attractive therapeutic target, and several antagonists and antibodies for this receptor were developed and are under clinical evaluation. Quantifying CXCR4 expression non-invasively might aid in prognostication as a mean for personalized therapy and post treatment monitoring. Multiple attempts were done over the recent years to develop imaging agents for CXCR4 using different technologies including PET, SPECT, fluorescent and bioluminescence, and will be reviewed in this paper.
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spelling pubmed-35630822013-02-04 Molecular Imaging of Chemokine Receptor CXCR4 Weiss, Ido. D. Jacobson, Orit Theranostics Review CXCR4 was found to be expressed by many different types of human cancers and its expression has been correlated with tumor aggressiveness, poor prognosis and resistance to chemotherapy. CXCR4 was also shown to contribute to metastatic seeding of organs that express its ligand CXCL12 and support the survival of these cells. These findings suggest that CXCR4 is a potentially attractive therapeutic target, and several antagonists and antibodies for this receptor were developed and are under clinical evaluation. Quantifying CXCR4 expression non-invasively might aid in prognostication as a mean for personalized therapy and post treatment monitoring. Multiple attempts were done over the recent years to develop imaging agents for CXCR4 using different technologies including PET, SPECT, fluorescent and bioluminescence, and will be reviewed in this paper. Ivyspring International Publisher 2013-01-15 /pmc/articles/PMC3563082/ /pubmed/23382787 http://dx.doi.org/10.7150/thno.4835 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Review
Weiss, Ido. D.
Jacobson, Orit
Molecular Imaging of Chemokine Receptor CXCR4
title Molecular Imaging of Chemokine Receptor CXCR4
title_full Molecular Imaging of Chemokine Receptor CXCR4
title_fullStr Molecular Imaging of Chemokine Receptor CXCR4
title_full_unstemmed Molecular Imaging of Chemokine Receptor CXCR4
title_short Molecular Imaging of Chemokine Receptor CXCR4
title_sort molecular imaging of chemokine receptor cxcr4
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563082/
https://www.ncbi.nlm.nih.gov/pubmed/23382787
http://dx.doi.org/10.7150/thno.4835
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