Tumor-associated antigens as possible targets for immune therapy in head and neck cancer:: Comparative mRNA expression analysis of RAGE and GAGE genes

被引:27
作者
Götte, K
Usener, D
Riedel, F
Hörmann, K
Schadendorf, D
Eichmüller, S
机构
[1] Univ Hosp Mannheim, Dept Otolaryngol Head & Neck Surg, DE-68135 Mannheim, Germany
[2] German Canc Res Ctr, Skin Canc Unit D0900, D-6900 Heidelberg, Germany
关键词
GAGE; head and neck cancer; RAGE; specific immune therapy; tumor-associated antigens;
D O I
10.1080/00016480260092381
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Specific immune therapy targeting residual areas of cancer cells may emerge as a powerful treatment strategy for head and neck squamous cell carcinoma (HNSCC). In order to define possible targets for immune therapy, we evaluated the frequency of two groups of tumor antigens-the RAGE and GAGE families-by means of reverse transcriptase polymerase chain reaction using primary HNSCCs (n=28), mucosa specimens as normal controls (n=10) and HNSCC cell lines (n=6). By means of specific primer selection we could differentiate between RAGE-1, -2, -3 and -4, as well as between two groups of GAGE genes (GAGE-1, 2,7 vs GAGE-3,4,5, 6,8). While all mucosa tissues (from smokers and non-smokers) were negative for bot h antigen families, 24: 28 investigated tumors were positive for up to 5 tumor antigens. Among the RAGE genes, RAGE-1-positive tumors were the most abundant (8: 28), followed by RAGE-2 (7/28) and RAGE-4 (6/28). Differences in the locations of HNSCCs were reflected by different RAGE family members being expressed most frequently: larynx, RAGE-1; oropharynx, RAGE-2; and hypopharynx, RAGE-4. Primers against GAGE-1, 2,7 and GAGE-3,4, 5,6, 8 revealed 6: 27 and 16: 27 positive tumors, respectively. This report suggests that RAGE genes and GAGE-3,4,5, 6,8 may be promising candidates for specific immune therapy in HNSCC.
引用
收藏
页码:546 / 552
页数:7
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