Using probes generated by chromosome microdissection and CGH findings, we have identified a series of chromosomal regions involved in human breast, ovarian and prostate cancer. In addition, it has been possible to determine the complex structure of homogeneously staining regions in several cases establishing that these structures are frequently composed of DNA segments derived from multiple chromosomes and intermingled to form an abnormal region. In order to isolate candidate target genes from these regions, we have developed a technique based on microdissection-mediated hybrid-selection of cDNAs. This technology, which supplements standard positional cloning techniques, has been utilized to isolate candidate genes from amplified regions on chromosome 13, 17, and 20 in breast cancer, as well as chromosome 12 in sarcomas. In addition, a novel tissue array technique has been developed which enables the simultaneous analysis of hundreds of cancer specimens for gene copy number and gene expression. The methodology previously described illustrates the importance of developing rapid techniques for the identification of genes amplified in a series of key human tumors. In addition to recognizing known sites of gene amplification, we have identifed several previously unidentified genes amplfied in breast, prostate and ovarian cancers. These genes will be utilized to determine the clinical signficance of gene amplification in various malignancies and their mechanism of action. It appears highly likely that important new information will be discovered relative to genes playing a causal role in disease genesis or progression.
| Wang, Qi; Anzick, Sarah; Richter, William F et al. (2004) Modulation of transcriptional sensitivity of mineralocorticoid and estrogen receptors. J Steroid Biochem Mol Biol 91:197-210 |
| Pollock, Pamela M; Cohen-Solal, Karine; Sood, Raman et al. (2003) Melanoma mouse model implicates metabotropic glutamate signaling in melanocytic neoplasia. Nat Genet 34:108-12 |
| Gorlick, Richard; Anderson, Peter; Andrulis, Irene et al. (2003) Biology of childhood osteogenic sarcoma and potential targets for therapeutic development: meeting summary. Clin Cancer Res 9:5442-53 |
| Goo, Young-Hwa; Sohn, Young Chang; Kim, Dae-Hwan et al. (2003) Activating signal cointegrator 2 belongs to a novel steady-state complex that contains a subset of trithorax group proteins. Mol Cell Biol 23:140-9 |
| Helman, Lee J; Meltzer, Paul (2003) Mechanisms of sarcoma development. Nat Rev Cancer 3:685-94 |
| Borden, Ernest C; Baker, Laurence H; Bell, Robert S et al. (2003) Soft tissue sarcomas of adults: state of the translational science. Clin Cancer Res 9:1941-56 |
| Anzick, Sarah L; Azorsa, David O; Simons Jr, S Stoney et al. (2003) Phenotypic alterations in breast cancer cells overexpressing the nuclear receptor co-activator AIB1. BMC Cancer 3:22 |
| Hedenfalk, Ingrid; Ringner, Markus; Ben-Dor, Amir et al. (2003) Molecular classification of familial non-BRCA1/BRCA2 breast cancer. Proc Natl Acad Sci U S A 100:2532-7 |
| Forozan, F; Veldman, R; Ammerman, C A et al. (1999) Molecular cytogenetic analysis of 11 new breast cancer cell lines. Br J Cancer 81:1328-34 |
