| Literature DB >> 16043716 |
Laszlo Radvanyi1, Devender Singh-Sandhu, Scott Gallichan, Corey Lovitt, Artur Pedyczak, Gustavo Mallo, Kurt Gish, Kevin Kwok, Wedad Hanna, Judith Zubovits, Jane Armes, Deon Venter, Jalil Hakimi, Jean Shortreed, Melinda Donovan, Mark Parrington, Pamela Dunn, Ray Oomen, James Tartaglia, Neil L Berinstein.
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.Entities:
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Year: 2005 PMID: 16043716 PMCID: PMC1182410 DOI: 10.1073/pnas.0500904102
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205