Skin Carcinogenesis Studies Using Mouse Models with Altered Polyamines.

Cancer growth and metastasis Pub Date : 2015-08-09 eCollection Date: 2015-01-01 DOI:10.4137/CGM.S21219
Shannon L Nowotarski, David J Feith, Lisa M Shantz
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引用次数: 19

Abstract

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.

Abstract Image

Abstract Image

使用改变多胺的小鼠模型进行皮肤癌研究。
非黑色素瘤皮肤癌(NMSC)是世界范围内的一个主要健康问题。随着器官移植受者和服用光敏药物的患者等高危人群数量的增加,NMSC的发病率持续上升。小鼠NMSC模型使我们能够更好地理解参与皮肤肿瘤发展的分子信号级联反应,从而确定新的治疗策略。在这里,我们回顾了旨在确定多胺在NMSC发展和维持中的作用的模型。肿瘤生长绝对需要升高的多胺,并且在NMSC中观察到其生物合成和分解代谢酶的失调。对表皮多胺基因改变小鼠的研究表明,它们在肿瘤促进和上皮细胞存活途径中发挥关键作用,最近的临床试验表明,多胺代谢的药理抑制剂在NMSC高风险个体中显示出希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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