Muller W J, Sinn E, Pattengale P K, Wallace R, Leder P
Harvard Medical School Department of Genetics, Boston, Massachusetts 02115.
Cell. 1988 Jul 1;54(1):105-15. doi: 10.1016/0092-8674(88)90184-5.
We have used transgenic mice that carry an activated c-neu oncogene driven by a mouse mammary tumor virus (MMTV) promoter to assess the stepwise progression of carcinogenesis in mammary epithelium. Unlike the stochastic occurrence of solitary mammary tumors in transgenic mice bearing the MMTV/c-myc or the MMTV/v-Ha-ras oncogenes, transgenic mice uniformly expressing the MMTV/c-neu gene develop mammary adenocarcinomas that involve the entire epithelium in each gland. Because these tumors arise synchronously and are polyclonal in origin, expression of the activated c-neu oncogene appears to be sufficient to induce malignant transformation in this tissue in a single step. In contrast, expression of the c-neu transgene in the parotid gland or epididymis leads to benign, bilateral epithelial hypertrophy and hyperplasia which does not progress to full malignant transformation during the observation period. These results indicate that the combination of activated oncogene and tissue context are major determinants of malignant progression and that expression of the activated form of c-neu in the mammary epithelium has particularly deleterious consequences.
我们利用携带由小鼠乳腺肿瘤病毒(MMTV)启动子驱动的激活型c-neu癌基因的转基因小鼠,来评估乳腺上皮细胞癌变的逐步进展过程。与携带MMTV/c-myc或MMTV/v-Ha-ras癌基因的转基因小鼠中孤立性乳腺肿瘤的随机发生不同,均匀表达MMTV/c-neu基因的转基因小鼠会发生乳腺腺癌,累及每个腺体的整个上皮组织。由于这些肿瘤同步出现且起源于多克隆,激活型c-neu癌基因的表达似乎足以在一步中诱导该组织发生恶性转化。相比之下,c-neu转基因在腮腺或附睾中的表达会导致良性的双侧上皮肥大和增生,在观察期内不会进展为完全的恶性转化。这些结果表明,激活的癌基因与组织环境的组合是恶性进展的主要决定因素,并且激活形式的c-neu在乳腺上皮中的表达具有特别有害的后果。