Selective cancer-germline gene expression in pediatric brain tumors

被引:23
作者
Jacobs, Joannes F. M. [2 ]
Grauer, Oliver M. [1 ,3 ]
Brasseur, Francis [4 ]
Hoogerbrugge, Peter M. [2 ]
Wesseling, Pieter [5 ,6 ]
Gidding, Corrie E. [2 ]
van de Rakt, Mandy W. M. M. [1 ]
Figdor, Carl G. [1 ]
Coulie, Pierre G. [7 ]
de Vries, I. Jolanda M. [1 ,2 ]
Adema, Gosse J. [1 ]
机构
[1] Nijmegen Ctr Mol Life Sci, Dept Tumor Immunol, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Dept Pediat Oncol, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[3] Univ Regensburg, Dept Neurol, Regensburg, Germany
[4] Ludwig Inst Canc Res, Brussels Branch, Brussels, Belgium
[5] Radboud Univ Nijmegen, Med Ctr, Dept Pathol, NL-6525 ED Nijmegen, Netherlands
[6] Canisius Wilhelmina Hosp, Dept Pathol, Nijmegen, Netherlands
[7] Catholic Univ Louvain, Christian Duve Inst Cellular Pathol, B-1200 Brussels, Belgium
关键词
brain tumor; pediatrics; qPCR; MAGE; NY-ESO-1; immune target;
D O I
10.1007/s11060-008-9577-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer-germline genes (CGGs) code for immunogenic antigens that are present in various human tumors and can be targeted by immunotherapy. Their expression has been studied in a wide range of human tumors in adults. We measured the expression of 12 CGGs in pediatric brain tumors, to identify targets for therapeutic cancer vaccines. Real Time PCR was used to quantify the expression of genes MAGE-A1, MAGE-A2, MAGE-A3, MAGE-A4, MAGE-A6, MAGE-A10, MAGE-A12, MAGE-C2, NY-ESO-1 and GAGE-1,2,8 in 50 pediatric brain tumors of different histological subtypes. Protein expression was examined with immunohistochemistry. Fifty-five percent of the medulloblastomas (n = 11), 86% of the ependymomas (n = 7), 40% of the choroid plexus tumors (n = 5) and 67% of astrocytic tumors (n = 27) expressed one or more CGGs. Immunohistochemical analysis confirmed qPCR results. With exception of a minority of tumors, the overall level of CGG expression in pediatric brain tumors was low. We observed a high expression of at least one CGG in 32% of the samples. CGG-encoded antigens are therefore suitable targets in a very selected group of pediatric patients with a brain tumor. Interestingly, glioblastomas from adult patients expressed CGGs more often and at significantly higher levels compared to pediatric glioblastomas. This observation is in line with the notion that pediatric and adult glioblastomas develop along different genetic pathways.
引用
收藏
页码:273 / 280
页数:8
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