AMD3100 protects from UV-induced skin cancer

Sunlight causes skin cancer by directly damaging DNA as well as by suppressing antitumor immune responses. A major mechanism whereby sunlight exerts immunosuppressive effects is by modulating the migration of chemokine (C-X-C motif) receptor 4 (CXCR4)-expressing dermal mast cells into and away from...

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Main Authors: Byrne, Scott N., Sarchio, Seri Narti Edayu
Format: Article
Published: Taylor & Francis 2014
Online Access:http://psasir.upm.edu.my/id/eprint/36376/
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spelling my.upm.eprints.363762015-08-21T02:35:58Z http://psasir.upm.edu.my/id/eprint/36376/ AMD3100 protects from UV-induced skin cancer Byrne, Scott N. Sarchio, Seri Narti Edayu Sunlight causes skin cancer by directly damaging DNA as well as by suppressing antitumor immune responses. A major mechanism whereby sunlight exerts immunosuppressive effects is by modulating the migration of chemokine (C-X-C motif) receptor 4 (CXCR4)-expressing dermal mast cells into and away from the skin. We have demonstrated the importance of this by showing that the systemic administration of the CXCR4 antagonist AMD3100 prevents sunlight-induced immunosuppression as well as the consequent carcinogenic response. Our results highlight the therapeutic potential of antagonizing CXCR4 signaling, especially in individuals who are at high risk of developing skin cancer. Taylor & Francis 2014 Article PeerReviewed Byrne, Scott N. and Sarchio, Seri Narti Edayu (2014) AMD3100 protects from UV-induced skin cancer. OncoImmunology, 3 (2). art. no. e27562. pp. 1-3. ISSN 2162-402X 10.4161/onci.27562
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
description Sunlight causes skin cancer by directly damaging DNA as well as by suppressing antitumor immune responses. A major mechanism whereby sunlight exerts immunosuppressive effects is by modulating the migration of chemokine (C-X-C motif) receptor 4 (CXCR4)-expressing dermal mast cells into and away from the skin. We have demonstrated the importance of this by showing that the systemic administration of the CXCR4 antagonist AMD3100 prevents sunlight-induced immunosuppression as well as the consequent carcinogenic response. Our results highlight the therapeutic potential of antagonizing CXCR4 signaling, especially in individuals who are at high risk of developing skin cancer.
format Article
author Byrne, Scott N.
Sarchio, Seri Narti Edayu
spellingShingle Byrne, Scott N.
Sarchio, Seri Narti Edayu
AMD3100 protects from UV-induced skin cancer
author_facet Byrne, Scott N.
Sarchio, Seri Narti Edayu
author_sort Byrne, Scott N.
title AMD3100 protects from UV-induced skin cancer
title_short AMD3100 protects from UV-induced skin cancer
title_full AMD3100 protects from UV-induced skin cancer
title_fullStr AMD3100 protects from UV-induced skin cancer
title_full_unstemmed AMD3100 protects from UV-induced skin cancer
title_sort amd3100 protects from uv-induced skin cancer
publisher Taylor & Francis
publishDate 2014
url http://psasir.upm.edu.my/id/eprint/36376/
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score 13.214268