Human breast cancer cells generated by oncogenic transformation of primary mammary epithelial cells
- Brian Elenbaas1,
- Lisa Spirio1,
- Frederick Koerner2,
- Mark D. Fleming3,
- Drazen B. Zimonjic4,
- Joana Liu Donaher1,
- Nicholas C. Popescu4,
- William C. Hahn1,5, and
- Robert A. Weinberg1,6
- 1Whitehead Institute for Biomedical Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA; 2Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA; 3Department of Pathology, Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA; 4Laboratory of Experimental Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892, USA; 5Department of Adult Oncology, Dana-Farber Cancer Institute, and Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA
Abstract
A number of genetic mutations have been identified in human breast cancers, yet the specific combinations of mutations required in concert to form breast carcinoma cells remain unknown. One approach to identifying the genetic and biochemical alterations required for this process involves the transformation of primary human mammary epithelial cells (HMECs) to carcinoma cells through the introduction of specific genes. Here we show that introduction of three genes encoding the SV40 large-T antigen, the telomerase catalytic subunit, and an H-Ras oncoprotein into primary HMECs results in cells that form tumors when transplanted subcutaneously or into the mammary glands of immunocompromised mice. The tumorigenicity of these transformed cells was dependent on the level of ras oncogene expression. Interestingly, transformation of HMECs but not two other human cell types was associated with amplifications of the c-myc oncogene, which occurred during the in vitro growth of the cells. Tumors derived from the transformed HMECs were poorly differentiated carcinomas that infiltrated through adjacent tissue. When these cells were injected subcutaneously, tumors formed in only half of the injections and with an average latency of 7.5 weeks. Mixing the epithelial tumor cells with Matrigel or primary human mammary fibroblasts substantially increased the efficiency of tumor formation and decreased the latency of tumor formation, demonstrating a significant influence of the stromal microenvironment on tumorigenicity. Thus, these observations establish an experimental system for elucidating both the genetic and cell biological requirements for the development of breast cancer.
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Footnotes
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↵6 Corresponding author.
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E-MAIL weinberg{at}wi.mit.edu; FAX (617) 258-5213.
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Article and publication are at www.genesdev.org/cgi/doi/10.1101/gad.828901.
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- Received June 21, 2000.
- Accepted November 10, 2000.
- Cold Spring Harbor Laboratory Press
