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Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines

Nonmelanoma skin cancer (NMSC) is a major health concern worldwide. With increasing numbers in high-risk groups such as organ transplant recipients and patients taking photosensitizing medications, the incidence of NMSC continues to rise. Mouse models of NMSC allow us to better understand the molecu...

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Autores principales: Nowotarski, Shannon L, Feith, David J, Shantz, Lisa M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558889/
https://www.ncbi.nlm.nih.gov/pubmed/26380554
http://dx.doi.org/10.4137/CGM.S21219
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author Nowotarski, Shannon L
Feith, David J
Shantz, Lisa M
author_facet Nowotarski, Shannon L
Feith, David J
Shantz, Lisa M
author_sort Nowotarski, Shannon L
collection PubMed
description Nonmelanoma skin cancer (NMSC) is a major health concern worldwide. With increasing numbers in high-risk groups such as organ transplant recipients and patients taking photosensitizing medications, the incidence of NMSC continues to rise. Mouse models of NMSC allow us to better understand the molecular signaling cascades involved in skin tumor development in order to identify novel therapeutic strategies. Here we review the models designed to determine the role of the polyamines in NMSC development and maintenance. Elevated polyamines are absolutely required for tumor growth, and dysregulation of their biosynthetic and catabolic enzymes has been observed in NMSC. Studies using mice with genetic alterations in epidermal polyamines suggest that they play key roles in tumor promotion and epithelial cell survival pathways, and recent clinical trials indicate that pharmacological inhibitors of polyamine metabolism show promise in individuals at high risk for NMSC.
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spelling pubmed-45588892015-09-17 Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines Nowotarski, Shannon L Feith, David J Shantz, Lisa M Cancer Growth Metastasis Review Nonmelanoma skin cancer (NMSC) is a major health concern worldwide. With increasing numbers in high-risk groups such as organ transplant recipients and patients taking photosensitizing medications, the incidence of NMSC continues to rise. Mouse models of NMSC allow us to better understand the molecular signaling cascades involved in skin tumor development in order to identify novel therapeutic strategies. Here we review the models designed to determine the role of the polyamines in NMSC development and maintenance. Elevated polyamines are absolutely required for tumor growth, and dysregulation of their biosynthetic and catabolic enzymes has been observed in NMSC. Studies using mice with genetic alterations in epidermal polyamines suggest that they play key roles in tumor promotion and epithelial cell survival pathways, and recent clinical trials indicate that pharmacological inhibitors of polyamine metabolism show promise in individuals at high risk for NMSC. Libertas Academica 2015-08-09 /pmc/articles/PMC4558889/ /pubmed/26380554 http://dx.doi.org/10.4137/CGM.S21219 Text en © 2015 the author(s), publisher and licensee Libertas Academica Ltd. This is an open-access article distributed under the terms of the Creative Commons CC-BY-NC 3.0 License.
spellingShingle Review
Nowotarski, Shannon L
Feith, David J
Shantz, Lisa M
Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines
title Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines
title_full Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines
title_fullStr Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines
title_full_unstemmed Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines
title_short Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines
title_sort skin carcinogenesis studies using mouse models with altered polyamines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558889/
https://www.ncbi.nlm.nih.gov/pubmed/26380554
http://dx.doi.org/10.4137/CGM.S21219
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