Opitz Oliver G, Quante Michael, von Werder Alexander, Heeg Steffen, Blum Hubert E
Department of Medicine II, University of Freiburg, Germany.
Onkologie. 2005 Jan;28(1):44-8. doi: 10.1159/000082039.
Squamous cancers of the oral cavity and esophagus are common worldwide. A number of environmental factors as well as genetic alterations have been identified. However, the specific combination of genetic events and their interplay with environmental carcinogens are largely un-known. Furthermore, no good animal model existed to study the molecular changes important in the induction and progression of the disease. Here we summarize the efforts made to establish a mouse model of oral-esophageal carcinogenesis. Cyclin D1 overexpressing(L2D1+) mice were generated using an EBV promoter to specifically target the oral cavity and the esophageal squamous epithelium. Besides analyzing different environmental factors, such as nitrosamines and zinc deficiency, cyclin D1 transgenic mice were crossbred with p53-deficient mice. While L2D1+ mice exhibited a phenotype of dysplasia, different combinations of mice result-ed in invasive oral-esophageal cancer. This mouse model provides a well-defined and reproducible model of oral-esophageal cancer that should be useful for testing chemopreventive, diagnostic, and therapeutic strategies.
口腔和食管癌的鳞状细胞癌在全球范围内都很常见。人们已经确定了许多环境因素以及基因改变。然而,基因事件的具体组合及其与环境致癌物的相互作用在很大程度上尚不清楚。此外,不存在用于研究该疾病诱导和进展过程中重要分子变化的良好动物模型。在此,我们总结了为建立口腔 - 食管癌发生小鼠模型所做的努力。使用EBV启动子产生细胞周期蛋白D1过表达(L2D1 +)小鼠,以特异性靶向口腔和食管鳞状上皮。除了分析不同的环境因素,如亚硝胺和锌缺乏外,细胞周期蛋白D1转基因小鼠还与p53缺陷小鼠进行杂交。虽然L2D1 +小鼠表现出发育异常的表型,但不同组合的小鼠会导致侵袭性口腔 - 食管癌。这种小鼠模型提供了一种明确且可重复的口腔 - 食管癌模型,应该有助于测试化学预防、诊断和治疗策略。