Smith Brittni A, Shelton Dawne N, Kieffer Collin, Milash Brett, Usary Jerry, Perou Charles M, Bernard Philip S, Welm Bryan E
Oncological Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Genes Cancer. 2012 Sep;3(9-10):550-63. doi: 10.1177/1947601913475359.
Human breast cancer is a heterogeneous disease composed of different histologies and molecular subtypes, many of which are not replicated in animal models. Here, we report a mouse model of breast cancer that generates unique tumor histologies including tubular, adenosquamous, and lipid-rich carcinomas. Utilizing a nononcogenic variant of polyoma middle T oncogene (PyMT) that requires a spontaneous base-pair deletion to transform cells, in conjunction with lentiviral transduction and orthotopic transplantation of primary mammary epithelial cells, this model sporadically induces oncogene expression in both the luminal and myoepithelial cell lineages of the normal mouse mammary epithelium. Microarray and hierarchical analyses using an intrinsic subtype gene set revealed that lentiviral PyMT generates both luminal and basal-like tumors. Cumulatively, these results show that low-level expression of PyMT in a broad range of cell types significantly increases tumor heterogeneity and establishes a mouse model of several rare human breast cancer subtypes.
人类乳腺癌是一种由不同组织学类型和分子亚型组成的异质性疾病,其中许多在动物模型中无法复制。在此,我们报告一种乳腺癌小鼠模型,该模型可产生独特的肿瘤组织学类型,包括管状癌、腺鳞癌和富含脂质的癌。利用多瘤病毒中间T癌基因(PyMT)的一种非致癌变体,该变体需要自发的碱基对缺失才能转化细胞,并结合慢病毒转导和原代乳腺上皮细胞的原位移植,此模型在正常小鼠乳腺上皮的管腔和肌上皮细胞谱系中偶尔诱导癌基因表达。使用内在亚型基因集进行的微阵列和层次分析表明,慢病毒PyMT可产生管腔型和基底样肿瘤。累积来看,这些结果表明,PyMT在广泛细胞类型中的低水平表达显著增加了肿瘤异质性,并建立了几种罕见人类乳腺癌亚型的小鼠模型。