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小鼠乳腺肿瘤发生过程中的癌前表型。

The preneoplastic phenotype in murine mammary tumorigenesis.

作者信息

Medina D

机构信息

Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

J Mammary Gland Biol Neoplasia. 2000 Oct;5(4):393-407. doi: 10.1023/a:1009529928422.

DOI:10.1023/a:1009529928422
PMID:14973384
Abstract

Preneoplastic lesions in murine mammary tumorigenesis have been extensively investigated over the past 50 years. The two general types of lesion that have malignant potential are the alveolar hyperplasias represented by the classical hyperplastic alveolar nodule and the ductal hyperplasias. The former type of lesion is induced by viral, chemical and hormonal agents; the latter by chemical agents and specific genetic alterations. Individual animal models have been utilized to elucidate the basic biological properties of the lesions and some of the basic molecular alterations. The biological phenotype of the two types of lesions include immortalization and epithelial hyperplasia. The ductal hyperplasias are distinguished from the alveolar hyperplasias by their pattern of epithelial hyperplasia and their extent of aneuploidy. The molecular alterations underlying epithelial hyperplasia are numerous and dependent on the particular animal model. An important issue for future studies is how faithfully any of these models mimic human premalignant progression. A minimal set of criteria is proposed that includes morphological progression, hormone dependence and genetic instability. It is likely that hyperplasias from a specific mouse model will represent a subset of the lesions found in human disease. Analogous hyperplasias from several defined genetic models, adequately characterized at the biological and molecular levels, would provide appropriate models for testing chemopreventive agents.

摘要

在过去50年里,对小鼠乳腺肿瘤发生过程中的癌前病变进行了广泛研究。具有恶性潜能的两种一般类型的病变是由经典增生性肺泡结节代表的肺泡增生和导管增生。前一种类型的病变由病毒、化学和激素因子诱导;后一种由化学因子和特定的基因改变诱导。已利用个体动物模型来阐明病变的基本生物学特性以及一些基本分子改变。这两种类型病变的生物学表型包括永生化和上皮增生。导管增生与肺泡增生的区别在于其上皮增生模式和非整倍体程度。上皮增生背后的分子改变众多,且取决于特定的动物模型。未来研究的一个重要问题是这些模型在多大程度上能够准确模拟人类癌前病变进展。提出了一套最低标准,包括形态学进展、激素依赖性和基因不稳定性。来自特定小鼠模型的增生可能代表人类疾病中发现的病变的一个子集。来自几个已定义遗传模型的类似增生,在生物学和分子水平上得到充分表征,将为测试化学预防剂提供合适的模型。

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