Hochwalt A E, Wirgin I, Felber M, Currie D D, Garte S J
Department of Environmental Medicine, New York University Medical Center, New York 10016.
Mol Carcinog. 1988;1(1):4-6. doi: 10.1002/mc.2940010104.
Rat nasal squamous cell carcinomas induced by inhalation of three direct-acting alkylating agents yielded DNA containing activated oncogenes with no homology to any member of the ras family. The novel NIH 3T3 transforming oncogenes from tumors induced by beta-propiolactone and methylmethane sulfonate are distinct from each other based on restriction analysis. The gene isolated from beta-propiolactone-induced tumors is between 6 and 9 kb in size. None of the tumors induced by dimethylcarbamyl chloride contained positive DNA in the NIH 3T3 focus assay or in the nude mouse cotransfection assay. The rat nasal tumor model is apparently ideally suited for analysis of the roles of carcinogen and tissue specificity in oncogene activation, especially related to novel (non-ras) transforming oncogenes.
吸入三种直接作用的烷化剂诱发的大鼠鼻鳞状细胞癌产生了含有活化癌基因的DNA,这些癌基因与ras家族的任何成员均无同源性。基于限制性分析,由β-丙内酯和甲磺酸甲酯诱发的肿瘤中分离出的新型NIH 3T3转化癌基因彼此不同。从β-丙内酯诱发的肿瘤中分离出的基因大小在6至9 kb之间。在NIH 3T3焦点试验或裸鼠共转染试验中,由二甲基氨基甲酰氯诱发的肿瘤均未含有阳性DNA。大鼠鼻肿瘤模型显然非常适合分析致癌物和组织特异性在癌基因激活中的作用,尤其是与新型(非ras)转化癌基因相关的作用。