Molecular cloning and immunogenicity of renal cell carcinoma-associated antigen G250

被引:34
作者
Grabmaier, K
Vissers, JLM
De Weijert, MCA
Oosterwijk-Wakka, JC
Van Bokhoven, A
Brakenhoff, RH
Noessner, E
Mulders, PA
Merkx, G
Figdor, CG
Adema, GJ
Oosterwijk, E
机构
[1] Univ Nijmegen Hosp, Dept Urol, Urol Res Lab, NL-6500 HB Nijmegen, Netherlands
[2] Univ Nijmegen Hosp, Dept Tumor Immunol, NL-6500 HB Nijmegen, Netherlands
[3] Univ Nijmegen Hosp, Dept Cytogenet, NL-6500 HB Nijmegen, Netherlands
[4] Univ Hosp Amsterdam, Dept Otolaryngol, Amsterdam, Netherlands
[5] Univ Munich, Inst Immunol, D-8000 Munich, Germany
关键词
D O I
10.1002/(SICI)1097-0215(20000315)85:6<865::AID-IJC21>3.0.CO;2-Q
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The molecular cloning of the cDNA and gene encoding the venal cell carcinoma (RCC)-associated protein G250 is described. This protein is one of the best markers for clear cell RCC: all clear-cell RCC express this protein, whereas no expression can be detected in normal kidney and most other normal tissue. Antibody studies have indicated that this molecule might serve as a therapeutic target. In view of the induction/up-regulation of G250 antigen in RCC, its restricted tissue expression and its possible role in therapy, we set out to molecularly define the G250 antigen, which we identified as a transmembrane protein identical to the tumor-associated antigen MN/CAIX. We determined, by FISH analysis, that the G250/MN/CAIX gene is located on chromosome 9p12-13. In view of the relative immunogenicity of RCC, we investigated whether the G250 antigen can be recognized by TIL derived from RCC patients. The initial characterization of 18 different TIL cultures suggests that anti-G250 reactivity is rare. (C) 2000 Wiley-Liss, Inc.
引用
收藏
页码:865 / 870
页数:6
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