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Issue title: Immunology of Breast Cancer
Guest editors: Wei-Zen Weix and Diana Lopezy
Article type: Research Article
Authors: Vlad, Anda M. | Finn, Olivera J.; *
Affiliations: Department of Immunology, University of Pittsburgh School of Medicine, E1040 Biomedical Science Tower, Pittsburgh, PA 15261, USA | [x] Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA | [y] Department of Microbiology and Immunology, University of Miami School of Medicine, Miami, FL 33136, USA
Correspondence: [*] Corresponding author: Olivera J. Finn, Department of Immunology, University of Pittsburgh School of Medicine, E1040 Biomedical Science Tower, Pittsburgh, PA 15261, USA. Tel.: +1 412 648 9816; Fax: +1 412 648 7042; E-mail: [email protected]
Abstract: Continued progress in breast cancer immunotherapy, in particular breast cancer vaccines, depends on the identification of target molecules aberrantly expressed on breast cancer cells. Many different approaches to antigen discovery, including the recent developments in genomics and proteomics, have favored identification of protein tumor antigens. While some of these molecules provide important peptide epitopes recognized by T cells and antibodies, they represent only a small minority of potential targets. Considering that the majority of the cell proteins and therefore tumor cell proteins are glycosylated, tumor glycopeptides represent more important tumor-specific targets. Protein glycosylation is known to be dysregulated in cancer cells, leading to the accumulation of tumor-specific glycoproteins actively involved in tumor progression and metastasis. In addition to understanding the glycobiology of tumor cells and identifying tumor-specific glycoprotein antigens, better understanding is required of how the innate and the adaptive immune systems handle processing, presentation and recognition of glycoprotein antigens. We discuss here some of the new therapeutic strategies for exploiting abnormal glycosylation pathways in tumors and using defined carbohydrate and/or glycoprotein tumor antigens in active specific immunotherapy of breast cancer.
DOI: 10.3233/BD-2004-20109
Journal: Breast Disease, vol. 20, no. 1, pp. 73-79, 2004
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