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Molecular Oncology, Markers, Clinical Correlates |
Departments of Internal Medicine, Division of Hematology and Oncology [K. L. v. G., S. D., Z. F. W., S. D. M.] and Radiation Oncology [S. P. E.], The University of Michigan Health System, Ann Arbor, Michigan 48109; Department of Cancer Biology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030 [Y. W., C. D. B.] National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892-4431 [H. R., S. C.]; University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan 48109 [K. L. v. G., S. D., Z. F. W., M. S., S. P. E., S. D. M.]
Inflammatory breast cancer is a rapidly growing, distinct form of locally advanced breast cancer that carries a guarded prognosis. To identify the genes that contribute to this aggressive phenotype, we compared under- and overexpressed sequences in an inflammatory breast tumor cell line with those of actively replicating normal human mammary epithelial cell lines using differential display. Of the 17 transcripts isolated and characterized from these experiments, overexpression of RhoC GTPase and loss of expression of a novel gene on 6q22, LIBC (lost in inflammatory breast cancer), were highly correlated (P < 0.0095 and P < 0.0013, respectively) with the inflammatory phenotype when a panel of archival inflammatory breast cancers was compared with noninflammatory stage III breast cancers by in situ hybridization. This study suggests two new molecular markers specific for inflammatory breast cancer.
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