Pharmacologically antagonizing the CXCR4-CXCL12 chemokine pathway with AMD3100 inhibits sunlight-induced skin cancer

One way sunlight causes skin cancer is by suppressing anti-tumor immunity. A major mechanism involves altering mast cell migration via the C-X-C motif chemokine receptor 4–C-X-C motif chemokine ligand 12 (CXCR4-CXCL12) chemokine pathway. We have discovered that pharmacologically blocking this pathwa...

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Main Authors: Sarchio, Seri Narti Edayu, Scolyer, Richard A., Beaugie, Clare, McDonald, David, Marsh-Wakefield, Felix, Halliday, Gary M., Byrne, Scott N.
Format: Article
Language:English
Published: Nature Publishing Group 2014
Online Access:http://psasir.upm.edu.my/id/eprint/34895/
http://psasir.upm.edu.my/id/eprint/34895/1/Pharmacologically%20antagonizing%20the%20CXCR4.pdf
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author Sarchio, Seri Narti Edayu
Scolyer, Richard A.
Beaugie, Clare
McDonald, David
Marsh-Wakefield, Felix
Halliday, Gary M.
Byrne, Scott N.
author_facet Sarchio, Seri Narti Edayu
Scolyer, Richard A.
Beaugie, Clare
McDonald, David
Marsh-Wakefield, Felix
Halliday, Gary M.
Byrne, Scott N.
author_sort Sarchio, Seri Narti Edayu
building UPM Institutional Repository
collection Online Access
description One way sunlight causes skin cancer is by suppressing anti-tumor immunity. A major mechanism involves altering mast cell migration via the C-X-C motif chemokine receptor 4–C-X-C motif chemokine ligand 12 (CXCR4-CXCL12) chemokine pathway. We have discovered that pharmacologically blocking this pathway with the CXCR4 antagonist AMD3100 prevents both UV radiation-induced immune suppression and skin cancer. The majority of control mice receiving UV-only developed histopathologically confirmed squamous cell carcinomas. In contrast, skin tumor incidence and burden was significantly lower in AMD3100-treated mice. Perhaps most striking was that AMD3100 completely prevented the outgrowth of latent tumors that occurred once UV irradiation ceased. AMD3100 protection from UV immunosuppression and skin cancer was associated with reduced mast cell infiltration into the skin, draining lymph nodes, and the tumor itself. Thus a major target of CXCR4 antagonism was the mast cell. Our results indicate that interfering with UV-induced CXCL12 by antagonizing CXCR4 significantly inhibits skin tumor development by blocking UV-induced effects on mast cells. Hence, the CXCR4-CXCL12 chemokine pathway is a novel therapeutic target in the prevention of UV-induced skin cancer.
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spelling upm-348952016-01-26T03:15:00Z http://psasir.upm.edu.my/id/eprint/34895/ Pharmacologically antagonizing the CXCR4-CXCL12 chemokine pathway with AMD3100 inhibits sunlight-induced skin cancer Sarchio, Seri Narti Edayu Scolyer, Richard A. Beaugie, Clare McDonald, David Marsh-Wakefield, Felix Halliday, Gary M. Byrne, Scott N. One way sunlight causes skin cancer is by suppressing anti-tumor immunity. A major mechanism involves altering mast cell migration via the C-X-C motif chemokine receptor 4–C-X-C motif chemokine ligand 12 (CXCR4-CXCL12) chemokine pathway. We have discovered that pharmacologically blocking this pathway with the CXCR4 antagonist AMD3100 prevents both UV radiation-induced immune suppression and skin cancer. The majority of control mice receiving UV-only developed histopathologically confirmed squamous cell carcinomas. In contrast, skin tumor incidence and burden was significantly lower in AMD3100-treated mice. Perhaps most striking was that AMD3100 completely prevented the outgrowth of latent tumors that occurred once UV irradiation ceased. AMD3100 protection from UV immunosuppression and skin cancer was associated with reduced mast cell infiltration into the skin, draining lymph nodes, and the tumor itself. Thus a major target of CXCR4 antagonism was the mast cell. Our results indicate that interfering with UV-induced CXCL12 by antagonizing CXCR4 significantly inhibits skin tumor development by blocking UV-induced effects on mast cells. Hence, the CXCR4-CXCL12 chemokine pathway is a novel therapeutic target in the prevention of UV-induced skin cancer. Nature Publishing Group 2014-04 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/34895/1/Pharmacologically%20antagonizing%20the%20CXCR4.pdf Sarchio, Seri Narti Edayu and Scolyer, Richard A. and Beaugie, Clare and McDonald, David and Marsh-Wakefield, Felix and Halliday, Gary M. and Byrne, Scott N. (2014) Pharmacologically antagonizing the CXCR4-CXCL12 chemokine pathway with AMD3100 inhibits sunlight-induced skin cancer. The Journal of Investigative Dermatology, 134 (4). pp. 1091-1100. ISSN 0022-202X; ESSN: 1523-1747 http://www.nature.com/jid/journal/v134/n4/abs/jid2013424a.html 10.1038/jid.2013.424
spellingShingle Sarchio, Seri Narti Edayu
Scolyer, Richard A.
Beaugie, Clare
McDonald, David
Marsh-Wakefield, Felix
Halliday, Gary M.
Byrne, Scott N.
Pharmacologically antagonizing the CXCR4-CXCL12 chemokine pathway with AMD3100 inhibits sunlight-induced skin cancer
title Pharmacologically antagonizing the CXCR4-CXCL12 chemokine pathway with AMD3100 inhibits sunlight-induced skin cancer
title_full Pharmacologically antagonizing the CXCR4-CXCL12 chemokine pathway with AMD3100 inhibits sunlight-induced skin cancer
title_fullStr Pharmacologically antagonizing the CXCR4-CXCL12 chemokine pathway with AMD3100 inhibits sunlight-induced skin cancer
title_full_unstemmed Pharmacologically antagonizing the CXCR4-CXCL12 chemokine pathway with AMD3100 inhibits sunlight-induced skin cancer
title_short Pharmacologically antagonizing the CXCR4-CXCL12 chemokine pathway with AMD3100 inhibits sunlight-induced skin cancer
title_sort pharmacologically antagonizing the cxcr4-cxcl12 chemokine pathway with amd3100 inhibits sunlight-induced skin cancer
url http://psasir.upm.edu.my/id/eprint/34895/
http://psasir.upm.edu.my/id/eprint/34895/
http://psasir.upm.edu.my/id/eprint/34895/
http://psasir.upm.edu.my/id/eprint/34895/1/Pharmacologically%20antagonizing%20the%20CXCR4.pdf