May 2007
Volume 48, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2007
TGF-Beta Induces Osteopontin in Uveal Melanoma Cells
Author Affiliations & Notes
  • A. H. Wolf
    Dept of Ophthalmology, University of Munich LMU, Munich, Germany
  • I. W. Reiniger
    Dept of Ophthalmology, University of Munich LMU, Munich, Germany
  • U. C. Schaller
    Dept of Ophthalmology, University of Munich LMU, Munich, Germany
  • D. Kook
    Dept of Ophthalmology, University of Munich LMU, Munich, Germany
  • A. J. Mueller
    Dept of Ophthalmology, Klinikum Augsburg, Augsburg, Germany
  • A. Kampik
    Dept of Ophthalmology, University of Munich LMU, Munich, Germany
  • U. C. Welge-Luessen
    Dept of Ophthalmology, University of Munich LMU, Munich, Germany
  • Footnotes
    Commercial Relationships A.H. Wolf, None; I.W. Reiniger, None; U.C. Schaller, None; D. Kook, None; A.J. Mueller, None; A. Kampik, None; U.C. Welge-Luessen, None.
  • Footnotes
    Support None.
Investigative Ophthalmology & Visual Science May 2007, Vol.48, 4760. doi:
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    • Get Citation

      A. H. Wolf, I. W. Reiniger, U. C. Schaller, D. Kook, A. J. Mueller, A. Kampik, U. C. Welge-Luessen; TGF-Beta Induces Osteopontin in Uveal Melanoma Cells. Invest. Ophthalmol. Vis. Sci. 2007;48(13):4760.

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

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Abstract

Purpose:: TGF-beta has been shown to have a tumor promoting effect in uveal melanoma. In carcinomas TGF-beta is thought to promote the ability to metastasize. Osteopontin (OPN) is a promising tumor marker for uveal melanoma and other malignancies. Aim of our study was to investigate the coherence of the TGF-beta and the OPN in uveal melanoma cells.

Methods:: Cells of 5 untreated uveal melanoma were grown until confluency. For specification of cells, immunohistological staining against S100, HMB-45 and OPN was performed. Confluent cells were then treated with TGF-beta at 1,0 mg/ml for 6 to 48 hrs. Concentrations of OPN were measured thereafter by quantititive RT-PCR.

Results:: All grown cells showed positive staining for S 100, HMB-45 and OPN. Concentrations of OPN increased markedly in 4 out of 5 uveal melanomas when treated with TGF-beta. Highest increase of OPN was found in cells treated for 24 hrs at 1mg/ml TGF-beta. At this concentration we found an up to 3-fold increase of OPN.

Conclusions:: TGF-beta induces OPN in uveal melanoma cells. Thus, elevated levels of OPN as found in patients with metastastatic uveal melanoma might be induced by increased TGF-beta. Our results point out the need to further investigate the role of TGF-beta in the genesis of uveal melanoma.

Keywords: melanoma • tumors • pathology: human 
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