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CT-X antigen expression in human breast cancer
- Source :
- Proceedings of the National Academy of Sciences. 106:13493-13498
- Publication Year :
- 2009
- Publisher :
- Proceedings of the National Academy of Sciences, 2009.
-
Abstract
- Cancer/testis (CT) genes are predominantly expressed in human germ line cells, but not somatic tissues, and frequently become activated in different cancer types. Several CT antigens have already proved to be useful biomarkers and are promising targets for therapeutic cancer vaccines. The aim of the present study was to investigate the expression of CT antigens in breast cancer. Using previously generated massively parallel signature sequencing (MPSS) data, together with 9 publicly available gene expression datasets, the expression pattern of CT antigens located on the X chromosome (CT-X) was interrogated. Whereas a minority of unselected breast cancers was found to contain CT-X transcripts, a significantly higher expression frequency was detected in estrogen and progesterone receptor (ER) negative breast cancer cell lines and primary breast carcinomas. A coordinated pattern of CT-X antigen expression was observed, with MAGEA and NY-ESO-1/CTAG1B being the most prevalent antigens. Immunohistochemical staining confirmed the correlation of CT-X antigen expression and ER negativity in breast tumors and demonstrated a trend for their coexpression with basal cell markers. Because of the limited therapeutic options for ER-negative breast cancers, vaccines based on CT-X antigens might prove to be useful.
- Subjects :
- CA15-3
Estrogen receptor
Breast Neoplasms
Biology
Massively parallel signature sequencing
Breast cancer
Antigen
Antigens, Neoplasm
medicine
Humans
Neoplasm Metastasis
Expressed Sequence Tags
Multidisciplinary
Membrane Proteins
Cancer
Biological Sciences
medicine.disease
Immunohistochemistry
Gene Expression Regulation, Neoplastic
Receptors, Estrogen
Tissue Array Analysis
Immunology
Cancer research
Cancer/testis antigens
Female
Receptors, Progesterone
Subjects
Details
- ISSN :
- 10916490 and 00278424
- Volume :
- 106
- Database :
- OpenAIRE
- Journal :
- Proceedings of the National Academy of Sciences
- Accession number :
- edsair.doi.dedup.....4c2b9f662cfc6d6f6a7261be4cb72ad9
- Full Text :
- https://doi.org/10.1073/pnas.0906840106