Basal-like breast cancer (BLBC) is an aggressive and deadly subtype of human breast cancer that is highly metastatic, displays stem-cell like features, and has limited treatment options. Therefore, developing and characterizing preclinical mouse models with tumors that resemble BLBC is important for human therapeutic development. is a potent oncogene that is aberrantly expressed in most human breast cancers. In the BK5.ATF3 mouse model, overexpression of in the basal epithelial cells of the mammary gland produces tumors that are characterized by activation of the Wnt/β-catenin signaling pathway. Here, we used RNA-Seq and microRNA (miRNA) microarrays to better define the molecular features of BK5.ATF3-derived mammary tumors. These analyses showed that these tumors share many characteristics of human BLBC including reduced expression of , , and and increased expression of , , and the genes encoding keratins 5, 6, and 17. An analysis of miRNA expression revealed reduced levels of and , leading to the upregulation of their target genes including both the pluripotency factors and as well as the cancer stem-cell-related gene . Finally, we show through knock-down experiments that may directly modulate expression. Taken together, our results indicate that the mouse mammary tumor model could provide a powerful model to define the molecular mechanisms leading to BLBC, identify the factors that contribute to its aggressiveness, and, ultimately, discover specific genes and gene networks for therapeutic targeting.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7956570PMC
http://dx.doi.org/10.3390/ijms22052353DOI Listing

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