The heterogeneity of human breast cancer has been well described at the morphological, molecular, and genomic levels. This heterogeneity presents one of the greatest obstacles in the effective treatment of breast cancer since the distinct forms of breast cancer that reflect distinct mechanisms of disease will require distinct therapies. Although mouse models of cancer have traditionally been used to simplify the study of human disease, we suggest that there are opportunities to also model the complexity and heterogeneity of human cancer. Here, we illustrate the similarities of mouse models to the human condition in the heterogeneity of both pathologies and gene expression. We then provide an illustration of the potential of gene expression analysis methods when used in conjunction with current treatment options to model individualized therapeutic regimes.
机构:
Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10021 USA
Pratilas, Christine A.
Solit, David B.
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机构:
Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
Mem Sloan Kettering Canc Ctr, Human Oncol & Pathogenesis Program, 1275 York Ave, New York, NY 10021 USAMem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10021 USA
机构:
Beth Israel Deaconess Med Ctr, Dept Radiat Oncol, Boston, MA 02215 USA
Harvard Med Sch, Boston, MA 02115 USABeth Israel Deaconess Med Ctr, Dept Radiat Oncol, Boston, MA 02215 USA
Schmidt, D. R.
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS,
2021,
111
(03):
: E253
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E254