May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
Osteopontin as a Serum Biomarker in Uveal Melanoma: A Pilot Study
Author Affiliations & Notes
  • J. Pe'er
    Department of Ophthalmology, Department of Mathematics, Statistics, and Computer Science,
    Hadassah University Hospital, Jerusalem, Israel
  • V. Barak
    Department of Oncology, Department of Pathology,
    Hadassah University Hospital, Jerusalem, Israel
  • I. Kalickman
    Department of Oncology, Department of Pathology,
    Hadassah University Hospital, Jerusalem, Israel
  • D. Majumdar
    Department of Ophthalmology, Department of Mathematics, Statistics, and Computer Science,
    University of Illinois at Chicago, Chicago, IL
  • A. Lin
    Department of Oncology, Department of Pathology,
    University of Illinois at Chicago, Chicago, IL
  • A.J. Maniotis
    Department of Oncology, Department of Pathology,
    University of Illinois at Chicago, Chicago, IL
  • S.S. Kadkol
    Department of Oncology, Department of Pathology,
    University of Illinois at Chicago, Chicago, IL
  • R. Folberg
    Department of Oncology, Department of Pathology,
    University of Illinois at Chicago, Chicago, IL
  • Footnotes
    Commercial Relationships  J. Pe'er, None; V. Barak, None; I. Kalickman, None; D. Majumdar, None; A. Lin, None; A.J. Maniotis, None; S.S. Kadkol, None; R. Folberg, None.
  • Footnotes
    Support  NIH Grant EY10457
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 4258. doi:
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      J. Pe'er, V. Barak, I. Kalickman, D. Majumdar, A. Lin, A.J. Maniotis, S.S. Kadkol, R. Folberg; Osteopontin as a Serum Biomarker in Uveal Melanoma: A Pilot Study . Invest. Ophthalmol. Vis. Sci. 2005;46(13):4258.

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

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Abstract

Abstract: : Purpose: Serum osteopontin levels correlate with aggressive behavior and metastasis in breast, ovarian and pancreatic cancers. This study was designed to explore the putative diagnostic role of serum osteopontin as a biomarker in the identification of patients with metastatic uveal melanoma. Methods: Serum osteopontin levels of patients who had been treated for primary uveal melanoma and who were disease–free for at least 10 years (n=16) and patients who had metastatic melanoma to the liver (n=12) were measured by an ELISA assay (Assay Designs, Ann Arbor, MI). In five of these patients, paired serum samples six months before and immediately after the appearance of metastasis were available for analysis. Results: The mean serum osteopontin level was 9.44 ng/ml (range: 3.7 – 30) in patients who were disease–free for at least 10 years versus the mean level of 27.97 ng/ml (range: 5.1 to 139) in patients with metastatic melanoma (p = 0.0074 by Kruskall–Wallis test). In the five patients who were disease–free after treatment of the primary and who subsequently developed liver metastases, the serum osteopontin level rose two– to nine–fold. Conclusions: In this pilot study, we detected significant differences in serum osteopontin levels between uveal melanoma patients who were disease–free for at least 10 years and patients with metastatic uveal melanoma to the liver. Serum osteopontin may be a useful non–invasive marker in patients with uveal melanoma, pending validation of sensitivity and specificity.

Keywords: melanoma • oncology • tumors 
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