We investigated in breast cancers the expression of the SART-1 gene encoding tumor rejection antigens. SART-1 mRNA was expressed in all of the samples tested. The SART-1 800 antigen was detectable in 20 of 50 (40%) breast cancer tissues and all breast cancer cell lines tested, but not in normal brea
Expression of the tumor-rejection antigen SART1 in brain tumors
โ Scribed by Toshihiro Imaizumi; Terukazu Kuramoto; Kazuko Matsunaga; Shigeki Shichijo; Shigeru Yutani; Minoru Shigemori; Koutaro Oizumi; Kyogo Itoh
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- French
- Weight
- 156 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
We have reported a tumor-rejection antigen, SART1 259 , possessing tumor epitopes capable of inducing cytotoxic T lymphocytes (CTLs) in epithelial-cancer patients. This study investigated the expression of SART1 259 antigen in brain tumors, to explore for a potential molecule for use in specific immunotherapy of patients with brain tumors. The SART1 259 antigen was detected in the cytosol fraction of 13 of 18 (72%) glioma cell lines and in 12 of 34 (35%) brain-tumor tissues, with a higher rate of expression among malignant gliomas (5/10, 50%) and schwannomas (3/4). HLA-A24-restricted and SART1-specific CTLs recognized the HLA-A24 ุ and SART1 259 ุ glioma cells, and the levels of recognition correlated both with HLA-A24-antigen expression level and with the concentration of the SART1 peptide antigen. Therefore, the SART1 259 antigen could be a target molecule for specific immunotherapy of patients with brain tumors expressing HLA-class-I antigens.
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