The gene associated with trichorhinophalangeal syndrome in humans is overexpressed in breast cancer |
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Authors: | Radvanyi Laszlo Singh-Sandhu Devender Gallichan Scott Lovitt Corey Pedyczak Artur Mallo Gustavo Gish Kurt Kwok Kevin Hanna Wedad Zubovits Judith Armes Jane Venter Deon Hakimi Jalil Shortreed Jean Donovan Melinda Parrington Mark Dunn Pamela Oomen Ray Tartaglia James Berinstein Neil L |
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Affiliation: | Sanofi Pasteur, Toronto, Ontario, Canada M2R 3T4. lradvanyi@mdanderson.org |
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Abstract: | A comprehensive differential gene expression screen on a panel of 54 breast tumors and >200 normal tissue samples using DNA microarrays revealed 15 genes specifically overexpressed in breast cancer. One of the most prevalent genes found was trichorhinophalangeal syndrome type 1 (TRPS-1), a gene previously shown to be associated with three rare autosomal dominant genetic disorders known as the trichorhinophalangeal syndromes. A number of corroborating methodologies, including in situ hybridization, e-Northern analysis using ORF EST (ORESTES) and Unigene EST abundance analysis, immunoblot and immunofluorescence analysis of breast tumor cell lines, and immunohistochemistry, confirmed the microarray findings. Immunohistochemistry analysis found TRPS-1 protein expressed in >90% of early- and late-stage breast cancer, including ductal carcinoma in situ and invasive ductal, lobular, and papillary carcinomas. The TRPS-1 gene is also immunogenic with processed and presented peptides activating T cells found after vaccination of HLA-A2.1 transgenic mouse. Human T cell lines from HLA-A*0201+ female donors exhibiting TRPS-1-specific cytotoxic T lymphocyte activity could also be generated. |
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