Kunimi K, Uchibayashi T, Hisazumi H
Department of Urology, School of Medicine, Kanazawa University.
Nihon Hinyokika Gakkai Zasshi. 1991 Dec;82(12):1924-9. doi: 10.5980/jpnjurol1989.82.1924.
The accumulating data have shown that a single or certain combinations of proto-oncogenes are genetically altered and acquire oncogenic activities in certain tumor types, through a point mutation and/or overexpression. In the present study, Northern blotting analysis was applied to clinical samples of renal cell carcinomas (RCC) to elucidate expression levels of the c-myc, c-fos and Harvey ras genes in this tumor form. In 11 cases of 23 tumors examined (48%) was shown more than 3-fold expression level of the c-myc gene compared with the matching normal RNA, the c-fos gene in 6 cases (26%), and the Harvey ras gene in one case (4%) showing the concomitant overexpression of two other genes. Overexpression of both the c-myc and c-fos genes was detected in 5 cases (22%). Although the distinct correlation between overexpressions of any genes and the clinical background was not induced, it is considered that these aberrations of proto-oncogenes are involved in oncogenesis of a certain subgroup of RCC.
越来越多的数据表明,在某些肿瘤类型中,单个原癌基因或某些原癌基因组合会通过点突变和/或过表达发生基因改变并获得致癌活性。在本研究中,采用Northern印迹分析技术检测肾细胞癌(RCC)临床样本中c-myc、c-fos和Harvey ras基因的表达水平。在检测的23例肿瘤中的11例(48%)中,与匹配的正常RNA相比,c-myc基因表达水平超过3倍,6例(26%)中c-fos基因表达水平超过3倍,1例(4%)中Harvey ras基因表达水平超过3倍,且这例同时伴有另外两个基因的过表达。5例(22%)中检测到c-myc和c-fos基因均过表达。虽然未发现任何基因过表达与临床背景之间存在明显相关性,但认为这些原癌基因的异常与RCC某一亚组的肿瘤发生有关。