Expression of multiple molecular phenotypes by aggressive melanoma tumor cells: Role in vasculogenic mimicry

Elisabeth A. Seftor, Paul S. Meltzer, Gina C. Schatteman, Lynn M. Gruman, Angela R. Hess, Dawn A. Kirschmann, Richard E.B. Seftor, Mary J.C. Hendrix*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

134 Scopus citations

Abstract

Cutaneous melanoma has been increasing at an alarming rate over the past two decades, however, there are no acceptable histopathological markers that classify various stages of melanoma progression. Recently, the molecular analysis of cancer has contributed significantly to our understanding of the cellular and molecular underpinnings of tumor progression. The data summarized in this review describe the molecular signature of aggressive cutaneous melanoma cells as that of multiple phenotypes which may be similar to a pluripotent, embryonic-like phenotype. An example of the plasticity of this phenotype is demonstrated by the ability of aggressive melanoma cells to engage in vasculogenic mimicry and neovascularization. A review of the current data demonstrating important cellular and molecular determinants of human melanoma vasculogenic mimicry is presented. These findings should stimulate additional studies to address the biological relevance of the multiple molecular phenotypes expressed by aggressive melanoma cells which may lead to the development of new diagnostic markers and therapeutic targets for clinical intervention.

Original languageEnglish (US)
Pages (from-to)17-27
Number of pages11
JournalCritical Reviews in Oncology/Hematology
Volume44
Issue number1
DOIs
StatePublished - Oct 1 2002

Funding

We gratefully acknowledge the gift of cutaneous melanoma cell lines from Julie Buckmeyer and Dr Frank Meyskens, Jr Research was supported by National Institutes of Health Grants CA59702 (Mary J.C. Hendrix), DK55965 (Gina C. Schatteman), and CA83137 (Richard E.B. Seftor).

Keywords

  • Epithelial cell kinase (ECK, EphA2)
  • Melanoma
  • Microarray
  • VE-cadherin
  • Vasculogenic mimicry

ASJC Scopus subject areas

  • Geriatrics and Gerontology
  • Hematology
  • Oncology

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