Visvanathan K V, Pocock R D, Summerhayes I C
Department of Cell and Molecular Biology, Institute of Cancer Research, Chester Beatty Laboratories, London, UK.
Oncogene Res. 1988;3(1):77-86.
In a survey of primary human bladder carcinomas from 24 patients, using the NIH/3T3 transfection nude mouse tumor assay, we have detected an activated c-H-ras-1 gene in four cases. Two of these scored negative in primary transfections using a NIH/3T3 focus assay. Oligonucleotide analysis of genomic and enzymatically amplified DNA revealed substitution of valine at codon 12 in DNA from three transfectants and their parental carcinomas, which was absent from the DNA of normal tissue of each of these patients. The fourth activation was identified as a cysteine substitution at codon 13, a novel activation of c-H-ras-1 in a solid tumor sample. Thus, all seven activated ras genes reported in human urothelial tumors (Fujita et al., Proc. Natl. Acad. Sci. USA 82, 3849-3853, 1985) have been c-H-ras-1 genes, strongly suggesting that this member of the ras gene family is preferentially activated in cells of transitional origin.
在一项对24例原发性人类膀胱癌的研究中,我们运用NIH/3T3转染裸鼠肿瘤检测法,在4例病例中检测到了激活的c-H-ras-1基因。其中2例在使用NIH/3T3集落形成检测法进行的初次转染中呈阴性。对基因组DNA和酶促扩增DNA进行的寡核苷酸分析显示,来自3个转染子及其亲本癌组织的DNA中,密码子12处的缬氨酸发生了取代,而这些患者的正常组织DNA中不存在这种情况。第4次激活被鉴定为密码子13处的半胱氨酸取代,这是在实体瘤样本中c-H-ras-1基因的一种新型激活。因此,人类尿路上皮肿瘤中报道的所有7个激活的ras基因(Fujita等人,《美国国家科学院院刊》82,3849 - 3853,1985年)均为c-H-ras-1基因,这强烈表明ras基因家族的这个成员在移行起源的细胞中优先被激活。