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Soluble MICA in malignant diseases

  • Stefan Holdenrieder
  • , Petra Stieber
  • , Andrea Peterfi
  • , Dorothea Nagel
  • , Alexander Steinle
  • , Helmut Rainer Salih
  • Ludwig-Maximilians-Universität München
  • Universitätsklinikum Tübingen
  • University of Tübingen

Research output: Contribution to journalArticlepeer-review

217 Scopus citations

Abstract

The immunoreceptor NKG2D activates natural killer cells and costimulates CD8 T cells. The MHC class I-related MICA molecules are ligands of NKG2D and are expressed on malignant, but not on normal, cells. As NKG2D plays an important role in the immunosurveillance of tumors, studies suggest that release of MICA from cancer cells constitutes an immune escape mechanism that systemically impairs antitumor immunity. Here, we investigated the potential of soluble MICA (sMICA) as a marker in cancer. Analysis of sMICA in sera of 512 individuals revealed significantly (p < 0.0001) higher levels in patients with various malignancies (n = 296, median 161 pg/ml) than in healthy individuals (n = 62, median <30 pg/ml). Patients with benign diseases (n = 154, median 84 pg/ml) exhibited intermediate sMICA levels. In cancer patients, elevated sMICA levels correlated significantly with cancer stage and metastasis (p = 0.015 and p = 0.007, respectively). While release of MICA is thought to impair tumor immunity, determination of sMICA levels may provide useful additional information in the diagnosis and staging of cancer.

Original languageEnglish
Pages (from-to)684-687
Number of pages4
JournalInternational Journal of Cancer
Volume118
Issue number3
DOIs
StatePublished - 1 Mar 2006
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Cancer
  • Diagnosis
  • MICA
  • NKG2D
  • Serum
  • Staging

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