Sakai H, Ogawa K
Department of Pathology, Asahikawa Medical College, Japan.
Int J Cancer. 1991 Aug 19;49(1):140-4. doi: 10.1002/ijc.2910490125.
Although administration of a single dose of N-nitroso-N-methylurea (NMU) to young virgin rats induces a high rate of mammary carcinomas, precise histogenesis of the carcinomas has not been well characterized. In this study, we investigated the alterations of H-ras gene in early focal lesions as well as carcinomas in the mammary glands of F344 rats treated with NMU. At 2 weeks after treatment, intraductal proliferation (IDP) was occasionally observed, and mammary carcinomas emerged at 12 and 36 weeks. The individual lesions of IDP and carcinomas were scooped out from the tissue sections under a stereomicroscope, and the DNA-sequence-spanning codon 12 of H-ras gene was amplified from the tissue sections by polymerase chain reaction (PCR). The analysis of amplified DNA by oligonucleotide hybridization revealed that 65% (11/17) of IDP and 89% (16/18) of carcinomas had a point mutation (G-to-A transition) at the 2nd position of H-ras codon 12. However, the DNA amplified from the areas, which appear histologically normal, never showed such mutation. These results indicate that IDP is a very early change for NMU-induced mammary carcinogenesis.
虽然给年轻的未交配大鼠单次注射N-亚硝基-N-甲基脲(NMU)可诱导出高发生率的乳腺癌,但这些癌的确切组织发生过程尚未得到很好的描述。在本研究中,我们调查了用NMU处理的F344大鼠乳腺中早期局灶性病变以及癌组织中H-ras基因的改变。处理后2周,偶尔观察到导管内增生(IDP),在12周和36周时出现乳腺癌。在体视显微镜下从组织切片中挖出IDP和癌的各个病变,通过聚合酶链反应(PCR)从组织切片中扩增H-ras基因跨越密码子12的DNA序列。通过寡核苷酸杂交对扩增的DNA进行分析,结果显示65%(11/17)的IDP和89%(16/18)的癌在H-ras密码子12的第2位有一个点突变(G到A的转换)。然而,从组织学上看似正常的区域扩增的DNA从未显示出这种突变。这些结果表明,IDP是NMU诱导的乳腺癌发生过程中非常早期的变化。