Novel products of the HUD, HUC, NNP-1 and α-internexin genes identified by autologous antibody screening of a pediatric neuroblastoma library

被引:13
作者
Behrends, U
Jandl, T
Golbeck, A
Lechner, B
Müller-Weihrich, S
Schmid, I
Till, H
Berthold, F
Voltz, R
Mautner, JM
机构
[1] Tech Univ Munich, Kinderklin, D-80804 Munich, Germany
[2] GSF Forschungszentrum Umwelt & Gesundheit, Inst Klin Mol & Tumorgenet, Klin Kooperat Grp Padiatr Tumorimmunol, Munich, Germany
[3] Univ Munich, Dr Von Haunerschen Kinderspital, D-80337 Munich, Germany
[4] Univ Cologne, Zentrum Padiatr Hamatol & Onkol, Cologne, Germany
[5] Univ Munich, Inst Klin Neuroimmunol, Munich, Germany
关键词
SEREX; neuroblastoma; tumor antigen; tumor marker; Hu syndrome;
D O I
10.1002/ijc.10550
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Autologous serological screening of a cDNA expression library (SEREX) derived from childhood neuroblastoma led to the identification of 10 different antigens, including 6 novel gene products. The novel antigen 0181NX was derived from a small open reading frame in a region of alpha-internexin mRNA that was previously described as 3' untranslated region. 0181NX thus represents a novel type of tumor antigen. Five novel gene products were derived from NNP-1 (NNP3) and Hu genes (HuC-L, HuD3, HuDY, HuD1pro(c)). As indicated by sequence analysis, these antigens were generated by alternative splicing and/or alternative promoter usage or allelic polymorphism. mRNA expression analyses revealed different tissue restrictions of novel compared to known HuD and NNP-1 transcripts in normal and malignant tissues. The expressions patterns of distinct transcripts indicated potential clinical meanings as diagnostic and/or prognostic tissue markers. When kinetics of serum antibody titres against SEREX-defined antigens were compared to tumor load over time in our patient with neuroblastoma, we found 100-fold increases of anti-Hu and anti-0181NX antibody titres preceding the clinical diagnosis of recurrent tumor growth after 2 years. When sera of pediatric patients with cancer (30) and healthy controls (30) were tested for humoral responses to SEREX-defined neuroblastoma antigens, we detected antibodies against all known antigens and NNP3 with low frequencies and titres in control sera, while anti-0181NX and anti-Hu antibodies were found in cancer patients only. Our findings indicate that SEREX-defined tumor antigens might provide novel tools for understanding and treatment of this aggressive childhood malignancy. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:669 / 677
页数:9
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