Biologic determinants of uveal melanoma metastatic phenotype: Role of intermediate filaments as predictive markers

Mary J.C. Hendrix*, Elisabeth A. Seftor, Richard E.B. Seftor, Lynn M. Gardner, H. Culver Boldt, Margaret Meyer, Jacob Pe'er, Robert Folberg

*Corresponding author for this work

Research output: Contribution to journalArticle

55 Scopus citations

Abstract

The long-range goal of our research is to develop intervention strategies based on newly discovered biologic mechanisms responsible for the invasive dissemination of metastatic uveal melanoma. To accomplish this goal, we have focused on the biologic relevance of novel marker proteins contributing to the uveal melanoma metastatic phenotype. The expression of vimentin intermediate filaments (IFs), a masenchymal marker, is typical of melanomas, whereas carcinomas typically express keratin IFs, which are markers for epithetia. Thus, cells that coaxpress both IFs are regarded as 'interconverted' in that they display both mesenchymal and epithelial phenotypes. Although the biologic functions of IFs have remained enigmatic, there is substantial support to suggest that the significance of vimentin/keratin coexpression is linked with poor patient outcome in cutaneous melanoma. Our data demonstrate that human uveal melanoma cell lines (isolated from primary choroidal or ciliary body melanomas and from foci of metastatic uveal melanoma to the liver), which contain predominant populations of cells that coaxpress vimentin/keratins 8 and 18 (keratins 8,18) IFs, were 6-fold more invasive through collagenous extracellular matrices in vitro, compared with uveal melanoma cells expressing vimentin only, and were 8- to 13-fold more invasive than normal uveal melanocytes. Colocalization of vimentin/keratins 8,18 in cell cultures was corroborated by immunohistochemistry in histologic sections of tumors from which the cell lines were derived. Minor populations of these cells also coexpressed keratins 13 and 17. Experimental down-regulation of the predominant keratins 8,18 in the interconverted cells, using 16-mer antisense oligonucleotides, resulted in a significant decrease in the migratory ability of the cells - similar to levels achieved by cells positive only for vimentin. These findings provide justification for additional studies of the association between coexpression of IFs vimentin/keratins 8,18 and uveal melanoma metastasis.

Original languageEnglish (US)
Pages (from-to)153-163
Number of pages11
JournalLaboratory Investigation
Volume78
Issue number2
StatePublished - Feb 1998

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Molecular Biology
  • Cell Biology

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    Hendrix, M. J. C., Seftor, E. A., Seftor, R. E. B., Gardner, L. M., Boldt, H. C., Meyer, M., Pe'er, J., & Folberg, R. (1998). Biologic determinants of uveal melanoma metastatic phenotype: Role of intermediate filaments as predictive markers. Laboratory Investigation, 78(2), 153-163.