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利用小鼠模型确定多胺在结肠癌发生中的作用。

Defining the role of polyamines in colon carcinogenesis using mouse models.

作者信息

Ignatenko Natalia A, Gerner Eugene W, Besselsen David G

机构信息

Department of Cell Biology and Anatomy, Arizona Cancer Center, 1515 N. Campbell Ave., Tucson, Arizona 85724, USA.

出版信息

J Carcinog. 2011;10:10. doi: 10.4103/1477-3163.79673. Epub 2011 Apr 16.

Abstract

Genetics and diet are both considered important risk determinants for colorectal cancer, a leading cause of death in the US and worldwide. Genetically engineered mouse (GEM) models have made a significant contribution to the characterization of colorectal cancer risk factors. Reliable, reproducible, and clinically relevant animal models help in the identification of the molecular events associated with disease progression and in the development of effictive treatment strategies. This review is focused on the use of mouse models for studying the role of polyamines in colon carcinogenesis. We describe how the available mouse models of colon cancer such as the multiple intestinal neoplasia (Min) mice and knockout genetic models facilitate understanding of the role of polyamines in colon carcinogenesis and help in the development of a rational strategy for colon cancer chemoprevention.

摘要

遗传学和饮食都被视为结直肠癌的重要风险决定因素,结直肠癌是美国和全球主要的死亡原因之一。基因工程小鼠(GEM)模型对结直肠癌风险因素的特征描述做出了重大贡献。可靠、可重复且与临床相关的动物模型有助于识别与疾病进展相关的分子事件,并有助于制定有效的治疗策略。本综述重点关注小鼠模型在研究多胺在结肠癌发生中的作用方面的应用。我们描述了现有的结肠癌小鼠模型,如多发性肠道肿瘤(Min)小鼠和基因敲除模型,如何促进对多胺在结肠癌发生中作用的理解,并有助于制定合理的结肠癌化学预防策略。

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