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Department of Pathology, Harvard Medical School, and the Molecular Pathology Unit, Massachusetts General Hospital, Boston, Massachusetts 02129 [D. C. S., R. L.]; Ophthalmology Research, Children’s Hospital, Boston, Massachusetts 02115 [G. R.]; and Microarray Department, Research Genetics, Inc., Huntsville, Alabama 35801 [S. T., J. R. H., A. G. E.]
The development and use of molecular-based therapy for breast cancer and other human malignancies will require a detailed molecular genetic analysis of patient tissues. The recent development of laser capture microdissection and high density cDNA arrays now provides a unique opportunity to generate gene expression profiles of cells from various stages of tumor progression as it occurs in the actual neoplastic tissue milieu. We report the combined use of laser capture microdissection and high-throughput cDNA microarrays to monitor in vivo gene expression levels in purified normal, invasive, and metastatic breast cell populations from a single patient. These in vivo gene expression profiles were verified by real-time quantitative PCR and immunohistochemistry. The combined use of laser capture microdissection and cDNA microarray analysis provides a powerful new approach to elucidate the in vivo molecular events surrounding the development and progression of breast cancer and is generally applicable to the study of malignancy.
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