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PMID: 6401381 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Ulex europaeus I lectin as a marker for tumors derived from endothelial cells.

American journal of clinical pathology ·Vol. 79 ·No. 1 ·1983-01-00 ·Pages 32-6

Miettinen M, Holthofer H, Lehto VP, Miettinen A, Virtanen I

Abstract

Some skin and soft tumors, which generally are assumed to be derived from endothelial cells or blood vessels, were characterized with fluorochrome-labeled Ulex europaeus I agglutinin (UEA I), recently shown to bind specifically to endothelial cells in various normal human tissues. The staining pattern was compared with that obtained with immunostaining using antibodies against factor-VIII-related antigen (FVIII-RAG), a known marker for endothelial cells. The results showed that UEA-I is a specific and a more sensitive marker for the endothelial cells in benign vascular lesions as compared with anti-FVIII-RAG. UEA-I also stained many neoplastic cells of endothelial sarcomas, which generally were negative for FVIII-RAG. Melanomas, anaplastic carcinomas, and other types of sarcomas were negative for both UEA-I and FVIII-RAG. The results suggest that UEA-I lectin is a specific and sensitive adjunct tool in demonstrating endothelial cells and endothelial derivation of human tumors.

MeSH Terms
Antigens/analysis Endothelium/pathology Factor VIII/analysis,immunology Hemangioma/pathology Hemangiopericytoma/pathology Hemangiosarcoma/pathology Humans Lectins Neoplasms, Vascular Tissue/pathology Plant Lectins Sarcoma, Kaposi/pathology Skin Neoplasms/pathology Soft Tissue Neoplasms/pathology von Willebrand Factor
Chemicals
Antigens Lectins Plant Lectins Ulex europaeus lectins von Willebrand Factor Factor VIII
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Miettinen M
Holthofer H
Lehto V P
Miettinen A
Virtanen I
Article Info
Journal
American journal of clinical pathology
Abbr.
Am J Clin Pathol
ISSN
0002-9173
Published
1983-01-00
Pages
32-6
Language
English
Region
England
NLM ID
0370470
Subset
IM
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