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The ELR(+)CXCL chemokines and their receptors CXCR1/CXCR2: A signaling axis and new target for the treatment of renal cell carcinoma
The long-term efficacy of anti-angiogenesis drugs targeting vascular endothelial growth factor (VEGF) and VEGF receptors in the treatment of renal cell carcinoma (RCC) has been lacking. We have shown that the ELR(+)CXCL cytokines and their (C-X-C) chemokine receptors, namely CXCR1 and CXCR2, stimula...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4063157/ https://www.ncbi.nlm.nih.gov/pubmed/25050209 http://dx.doi.org/10.4161/onci.28399 |
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author | Giuliano, Sandy Guyot, Mélanie Grépin, Renaud Pagès, Gilles |
author_facet | Giuliano, Sandy Guyot, Mélanie Grépin, Renaud Pagès, Gilles |
author_sort | Giuliano, Sandy |
collection | PubMed |
description | The long-term efficacy of anti-angiogenesis drugs targeting vascular endothelial growth factor (VEGF) and VEGF receptors in the treatment of renal cell carcinoma (RCC) has been lacking. We have shown that the ELR(+)CXCL cytokines and their (C-X-C) chemokine receptors, namely CXCR1 and CXCR2, stimulate cancer cell proliferation, tumor inflammation, and angiogenesis. Hence, this essential molecular nexus regulating cancer growth represents a key therapeutic target. |
format | Online Article Text |
id | pubmed-4063157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-40631572015-04-09 The ELR(+)CXCL chemokines and their receptors CXCR1/CXCR2: A signaling axis and new target for the treatment of renal cell carcinoma Giuliano, Sandy Guyot, Mélanie Grépin, Renaud Pagès, Gilles Oncoimmunology Author's View The long-term efficacy of anti-angiogenesis drugs targeting vascular endothelial growth factor (VEGF) and VEGF receptors in the treatment of renal cell carcinoma (RCC) has been lacking. We have shown that the ELR(+)CXCL cytokines and their (C-X-C) chemokine receptors, namely CXCR1 and CXCR2, stimulate cancer cell proliferation, tumor inflammation, and angiogenesis. Hence, this essential molecular nexus regulating cancer growth represents a key therapeutic target. Landes Bioscience 2014-04-09 /pmc/articles/PMC4063157/ /pubmed/25050209 http://dx.doi.org/10.4161/onci.28399 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Author's View Giuliano, Sandy Guyot, Mélanie Grépin, Renaud Pagès, Gilles The ELR(+)CXCL chemokines and their receptors CXCR1/CXCR2: A signaling axis and new target for the treatment of renal cell carcinoma |
title | The ELR(+)CXCL chemokines and their receptors CXCR1/CXCR2: A signaling axis and new target for the treatment of renal cell carcinoma |
title_full | The ELR(+)CXCL chemokines and their receptors CXCR1/CXCR2: A signaling axis and new target for the treatment of renal cell carcinoma |
title_fullStr | The ELR(+)CXCL chemokines and their receptors CXCR1/CXCR2: A signaling axis and new target for the treatment of renal cell carcinoma |
title_full_unstemmed | The ELR(+)CXCL chemokines and their receptors CXCR1/CXCR2: A signaling axis and new target for the treatment of renal cell carcinoma |
title_short | The ELR(+)CXCL chemokines and their receptors CXCR1/CXCR2: A signaling axis and new target for the treatment of renal cell carcinoma |
title_sort | elr(+)cxcl chemokines and their receptors cxcr1/cxcr2: a signaling axis and new target for the treatment of renal cell carcinoma |
topic | Author's View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4063157/ https://www.ncbi.nlm.nih.gov/pubmed/25050209 http://dx.doi.org/10.4161/onci.28399 |
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