首页   按字顺浏览 期刊浏览 卷期浏览 Expression of the SART1 tumor‐rejection antigens in colorectal cancers
Expression of the SART1 tumor‐rejection antigens in colorectal cancers

 

作者: Teruo Sasatomi,   Hideaki Yamana,   Shigeki Shichijo,   Shoko Tanaka,   Torahiko Okamura,   Yutaka Ogata,   Kyogo Itoh,   Kazuo Shirouzu,  

 

期刊: Diseases of the Colon & Rectum  (OVID Available online 2000)
卷期: Volume 43, issue 12  

页码: 1754-1758

 

ISSN:0012-3706

 

年代: 2000

 

出版商: OVID

 

关键词: Colorectal cancer;SART1;Tumor‐rejection antigen;CTL;Specific immunotherapy

 

数据来源: OVID

 

摘要:

PURPOSE:Colorectal cancer is one of the major causes of cancer death in the world, including in the United States and Japan. We recently identified the tumor‐rejection antigen gene SART1, which encodes both the SART1259antigen expressed in the cytosol of epithelial cancers and the SART1800antigen expressed in the nucleus of the majority of proliferating cells. This study investigated the expression of these tumor antigens to explore a potential molecule for specific immunotherapy of colorectal cancer patients.METHODS:SART1 antigens were investigated by Western blotting in six colorectal cancer cell lines and in 33 colorectal cancer tissues. The cancer cell lines were tested for their ability to stimulate interferon‐&ggr; production by the human‐leukocyte‐antigen‐A24‐restricted and SART1‐specific cytotoxic T lymphocytes and were also tested for their susceptibility to the lysis by the cytotoxic T lymphocytes.RESULTS:The SART1259antigen was detected in the cytosol of four of six cancer cell lines, 13 of 33 (39 percent) cancer tissues, and 0 of 20 nontumorous colorectal tissues. The SART1800antigen was expressed in the nucleus of all the colorectal cancer cell lines, 18 of 33 (55 percent) cancer tissues, and 0 of 20 nontumorous tissues. The human‐lymphocyte‐antigen‐A24‐restricted and SART1‐specific cytotoxic T lymphocytes killed the human‐lymphocyte‐antigen‐A24+SART1259+cancer cells.CONCLUSIONS:The SART1259antigen could be an appropriate target molecule for specific immunotherapy of approximately 40 percent of the human‐lymphocyte‐antigen‐A24+patients with colorectal cancer.

 

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