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Small Molecule Inhibitors of CXCR4

CXCR4 is a G-protein-coupled receptor involved in a number of physiological processes in the hematopoietic and immune systems. The SDF-1/CXCR4 axis is significantly associated with several diseases, such as HIV, cancer, WHIM syndrome, rheumatoid arthritis, pulmonary fibrosis and lupus. For example,...

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Detalles Bibliográficos
Autores principales: Debnath, Bikash, Xu, Shili, Grande, Fedora, Garofalo, Antonio, Neamati, Nouri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563081/
https://www.ncbi.nlm.nih.gov/pubmed/23382786
http://dx.doi.org/10.7150/thno.5376
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author Debnath, Bikash
Xu, Shili
Grande, Fedora
Garofalo, Antonio
Neamati, Nouri
author_facet Debnath, Bikash
Xu, Shili
Grande, Fedora
Garofalo, Antonio
Neamati, Nouri
author_sort Debnath, Bikash
collection PubMed
description CXCR4 is a G-protein-coupled receptor involved in a number of physiological processes in the hematopoietic and immune systems. The SDF-1/CXCR4 axis is significantly associated with several diseases, such as HIV, cancer, WHIM syndrome, rheumatoid arthritis, pulmonary fibrosis and lupus. For example, CXCR4 is one of the major co-receptors for HIV entry into target cells, while in cancer it plays an important role in tumor cell metastasis. Several promising CXCR4 antagonists have been developed to block SDF-1/CXCR4 interactions that are currently under different stages of development. The first in class CXCR4 antagonist, plerixafor, was approved by the FDA in 2008 for the mobilization of hematopoietic stem cells and several other drugs are currently in clinical trials for cancer, HIV, and WHIM syndrome. While the long-term safety data for the first generation CXCR4 antagonists are not yet available, several new compounds are under preclinical development in an attempt to provide safer and more efficient treatment options for HIV and cancer patients.
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spelling pubmed-35630812013-02-04 Small Molecule Inhibitors of CXCR4 Debnath, Bikash Xu, Shili Grande, Fedora Garofalo, Antonio Neamati, Nouri Theranostics Review CXCR4 is a G-protein-coupled receptor involved in a number of physiological processes in the hematopoietic and immune systems. The SDF-1/CXCR4 axis is significantly associated with several diseases, such as HIV, cancer, WHIM syndrome, rheumatoid arthritis, pulmonary fibrosis and lupus. For example, CXCR4 is one of the major co-receptors for HIV entry into target cells, while in cancer it plays an important role in tumor cell metastasis. Several promising CXCR4 antagonists have been developed to block SDF-1/CXCR4 interactions that are currently under different stages of development. The first in class CXCR4 antagonist, plerixafor, was approved by the FDA in 2008 for the mobilization of hematopoietic stem cells and several other drugs are currently in clinical trials for cancer, HIV, and WHIM syndrome. While the long-term safety data for the first generation CXCR4 antagonists are not yet available, several new compounds are under preclinical development in an attempt to provide safer and more efficient treatment options for HIV and cancer patients. Ivyspring International Publisher 2013-01-15 /pmc/articles/PMC3563081/ /pubmed/23382786 http://dx.doi.org/10.7150/thno.5376 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
Debnath, Bikash
Xu, Shili
Grande, Fedora
Garofalo, Antonio
Neamati, Nouri
Small Molecule Inhibitors of CXCR4
title Small Molecule Inhibitors of CXCR4
title_full Small Molecule Inhibitors of CXCR4
title_fullStr Small Molecule Inhibitors of CXCR4
title_full_unstemmed Small Molecule Inhibitors of CXCR4
title_short Small Molecule Inhibitors of CXCR4
title_sort small molecule inhibitors of cxcr4
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563081/
https://www.ncbi.nlm.nih.gov/pubmed/23382786
http://dx.doi.org/10.7150/thno.5376
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