O'Brien T G, Megosh L C, Gilliard G, Soler A P
The Lankenau Medical Research Center, Wynnewood, Pennsylvania 19096, USA.
Cancer Res. 1997 Jul 1;57(13):2630-7.
In multistage tumorigenesis models, ornithine decarboxylase (ODC) is usually dysregulated at some point during tumor promotion, an early stage of carcinogenesis. To address the question whether constitutive overexpression of ODC would be a sufficient condition for tumor promotion, mice with high levels of ODC expression targeted to epidermal keratinocytes were used in skin tumorigenesis experiments. Transgenic mice with ODC targeted to hair follicle keratinocytes were much more sensitive than littermate controls to initiation with a single low dose of carcinogen; in fact, such mice no longer required treatment with tumor promoters for tumors to develop. Targeting ODC overexpression to both interfollicular and follicular keratinocytes did not further enhance tumor yield. Our results suggest that most, if not all, target cells for chemical carcinogens in the skin reside in hair follicles, and ODC overexpression is sufficient to activate such cells to expand clonally to form epidermal tumors.
在多阶段肿瘤发生模型中,鸟氨酸脱羧酶(ODC)在肿瘤促进阶段(癌变的早期阶段)的某些时候通常会失调。为了解决ODC的组成型过表达是否足以促进肿瘤发生这一问题,在皮肤肿瘤发生实验中使用了ODC高水平表达靶向表皮角质形成细胞的小鼠。ODC靶向毛囊角质形成细胞的转基因小鼠比同窝对照对单次低剂量致癌物引发更敏感;事实上,这类小鼠不再需要用肿瘤促进剂处理就能发生肿瘤。将ODC过表达靶向到毛囊间和毛囊角质形成细胞并没有进一步提高肿瘤发生率。我们的结果表明,皮肤中化学致癌物的大多数(如果不是全部)靶细胞存在于毛囊中,ODC过表达足以激活这类细胞进行克隆性扩增以形成表皮肿瘤。