May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
S100B, S100 Dimers and Melanoma–Inhibitory Activity in Uveal Melanoma Screening Comparison With Liver Function Tests
Author Affiliations & Notes
  • G. Missotten
    Ophthalmology, Leiden Univ Med Ctr, Leiden, The Netherlands
  • N. Schalij–Delfos
    Ophthalmology, Leiden Univ Med Ctr, Leiden, The Netherlands
  • J.E. E. Keunen
    Ophthalmology, Leiden Univ Med Ctr, Leiden, The Netherlands
  • J.M. Bonfrer
    Clinical Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands
  • M.J. Jager
    Ophthalmology, Leiden Univ Med Ctr, Leiden, The Netherlands
  • Footnotes
    Commercial Relationships  G. Missotten, None; N. Schalij–Delfos, None; J.E.E. Keunen, None; J.M. Bonfrer, None; M.J. Jager, None.
  • Footnotes
    Support  Dutch Cancer Society
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 3388. doi:
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      G. Missotten, N. Schalij–Delfos, J.E. E. Keunen, J.M. Bonfrer, M.J. Jager; S100B, S100 Dimers and Melanoma–Inhibitory Activity in Uveal Melanoma Screening Comparison With Liver Function Tests . Invest. Ophthalmol. Vis. Sci. 2005;46(13):3388.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Abstract: : Purpose: To determine whether S100 protein, its dimers or MIA were present in the serum of patients with large uveal melanoma, an whether their concentrations were related to any clinical and histopathological parameters or to survival in these patients. We furthermore studied whether S100 protein or MIA may be better a indicator of micrometastases than liver function tests. Methods: S100B, S100A1B, S100BB and MIA concentration were measured in sera from 107 patients with uveal melanoma obtained prior to enucleation, from 30 uveal melanoma patients with metastases, and in sera from 50 healthy controls. The S100B Liaison, an immunoluminometric assay and S100B, S100A1B, S100BB and MIA ELISAs were used to quantify S100 and MIA concentrations in serum. Results were compared with liver function tests (AP, LDH, ASAT, ALAT and γGT). Results: S100B, S100 dimers and MIA were not significantly increased in sera from uveal melanoma patients at the moment of enucleation and were not related to clinical or histopathological parameters. There was, however, a significant difference between S100 and MIA in uveal melanoma patients with metastases compared to controls and patients without metastases. Both S100 and MIA showed a better correlation with the presence of metastatic disease better than liver function tests. Conclusions: In our study on uveal melanoma patients, S100B and MIA serum concentrations were not correlated with any tested tumour parameter and were not of prognostic value themselves, in contrast with findings in cutaneous melanoma. S100B and MIA were more sensitive than LDH and AP in identifying the presence of melanoma metastases. A prospective study is needed to evaluate S100B and MIA in identifying early micro–metastases in uveal melanoma.

Keywords: uvea • melanoma • clinical (human) or epidemiologic studies: systems/equipment/techniques 
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