Pelling J C, Neades R, Strawhecker J
Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha 68105.
Carcinogenesis. 1988 Apr;9(4):665-7. doi: 10.1093/carcin/9.4.665.
Previous results in a number of laboratories have demonstrated that epidermal papillomas and carcinomas induced by the two-stage protocol of initiation and promotion contain a point mutation in the 61st codon of the c-Ha-ras oncogene when the initiating agent used is 7,12-dimethylbenz[a]anthracene (DMBA). In the present report, we have analyzed DNA purified from 'spontaneously initiated' papillomas and carcinomas induced in SENCAR mouse epidermis after repetitive treatments with a tumor-promoting agent. Southern blot hybridization studies of tumor DNA digested with diagnostic restriction endonucleases demonstrated that seven of nine papillomas and carcinomas contained a point mutation in the 61st codon of one allele of the c-Ha-ras oncogene. The implications of our findings with respect to the role which a point-mutated Ha-ras proto-oncogene plays in initiation of skin tumorigenesis are discussed.
多个实验室之前的研究结果表明,当起始剂为7,12-二甲基苯并[a]蒽(DMBA)时,通过启动和促进的两阶段方案诱导的表皮乳头状瘤和癌在c-Ha-ras癌基因的第61密码子处存在点突变。在本报告中,我们分析了用促癌剂重复处理后在SENCAR小鼠表皮中诱导产生的“自发启动”乳头状瘤和癌的纯化DNA。用诊断性限制性内切酶消化肿瘤DNA的Southern印迹杂交研究表明,9个乳头状瘤和癌中有7个在c-Ha-ras癌基因一个等位基因的第61密码子处存在点突变。本文讨论了我们的研究结果对于点突变的Ha-ras原癌基因在皮肤肿瘤发生起始过程中所起作用的意义。