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

  • Uta Behrends
  • , Thomas Jandl
  • , Anja Golbeck
  • , Brigitte Lechner
  • , Stephan Müller-Weihrich
  • , Irene Schmid
  • , Holger Till
  • , Frank Berthold
  • , Raymond Voltz
  • , Josef M. Mautner
  • Technical University of Munich
  • Ludwig Maximilian University of Munich
  • University of Cologne
  • Helmholtz Zentrum München - German Research Center for Environmental Health

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

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 α-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, HuD1proc). 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.

Original languageEnglish
Pages (from-to)669-677
Number of pages9
JournalInternational Journal of Cancer
Volume100
Issue number6
DOIs
StatePublished - Aug 20 2002

Keywords

  • Hu syndrome
  • Neuroblastoma
  • SEREX
  • Tumor antigen
  • Tumor marker

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