Cardiff R D, Moghanaki D, Jensen R A
Department of Pathology and Center for Comparative Medicine, University of California, Davis 95616, USA.
J Mammary Gland Biol Neoplasia. 2000 Oct;5(4):421-37. doi: 10.1023/a:1009534129331.
Foci of atypical mammary epithelium have been associated with breast cancer in many species including mouse and man. The advent of targeted genomics has led to the creation of numerous genetically engineered mice (GEM) which display focal atypical lesions associated with mammary cancer. Some early lesions in GEM have a remarkable morphological similarity to pre-cancers in humans. While the malignant potential of atypical foci have been thoroughly documented in the non-GEM by tissue transplantation, a review of the literature reveals that precursor lesions in GEM remain incompletely described and only partially documented. Their validation as appropriate models of human breast preneoplasia awaits classical transplantation studies. Here, we review the literature characterizing early lesions of GEM models of mammary cancer, discuss the principles of the Focality, Atypia, and Association and present an introduction of mammary transplantation for model Validation.
非典型乳腺上皮灶已在包括小鼠和人类在内的许多物种中与乳腺癌相关联。靶向基因组学的出现导致了众多基因工程小鼠(GEM)的产生,这些小鼠表现出与乳腺癌相关的局灶性非典型病变。GEM中的一些早期病变在形态上与人类的癌前病变有显著相似性。虽然非基因工程小鼠中的非典型病灶的恶性潜能已通过组织移植得到充分记录,但文献综述表明,GEM中的前体病变仍描述不完整且仅有部分记录。它们作为人类乳腺肿瘤前病变的合适模型的验证有待经典移植研究。在此,我们综述了表征乳腺癌GEM模型早期病变的文献,讨论了局灶性、非典型性和关联性的原则,并介绍了用于模型验证的乳腺移植。