A Novel Mouse Model that Recapitulates the Heterogeneity of Human Triple Negative Breast Cancer
Doha, Z. O.; Wang, X.; Calistri, N.; Eng, J.; Daniel, C. J.; Ternes, L.; Kim, E. N.; Pelz, C.; Munks, M.; Betts, C.; Kirchberger, N.; Kwon, S.; Bucher, E.; Li, X.; Waugh, T.; Pietenpol, J. A.; Sanders, M. E.; Mills, G. B.; Chin, K.; Chang, Y. H.; Coussens, L. M.; Gray, J. W.; Heiser, L.; Sears, R. C.
Show abstract
Triple-negative breast cancer (TNBC) patients have a poor prognosis and few treatment options. Mouse models of TNBC are important for development of new targeted therapies, but few TNBC mouse models exist. Here, we developed a novel TNBC murine model by mimicking two common TNBC mutations with high co-occurrence: amplification of the oncogene MYC and deletion of the tumor suppressor PTEN. This Myc;Ptenfl murine model develops TN mammary tumors that display histological and molecular features commonly found in human TNBC. We performed deep omic analyses on Myc;Ptenfl tumors including machine learning for morphologic features, bulk and single-cell RNA-sequencing, multiplex immunohistochemistry and single-cell phenotyping. Through comparison with human TNBC, we demonstrated that this new genetic mouse model develops mammary tumors with differential survival that closely resemble the inter- and intra-tumoral and microenvironmental heterogeneity of human TNBC; providing a unique pre-clinical tool for assessing the spectrum of patient TNBC biology and drug response. Statement of significanceThe development of cancer models that mimic triple-negative breast cancer (TNBC) microenvironment complexities is critical to develop effective drugs and enhance disease understanding. This study addresses a critical need in the field by identifying a murine model that faithfully mimics human TNBC heterogeneity and establishing a foundation for translating preclinical findings into effective human clinical trials.
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