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Controlling tumor-derived and vascular endothelial cell growth: role of the 4Ff2 cell surface antigen.

Abstract
We have isolated a monoclonal antibody, clone betaE11, which recognizes an antigen that is highly abundant on the surface of mitotic vascular endothelial cells and tumor cells. By sodium dodecyl sulfate-polyacrylamide gel electrophoresis and Western blotting, expression of this 190-kd antigen is approximately threefold higher in mitotic versus interphase endothelial cells. Treatment of tumor cells with an antibody to the betaE11 antigen inhibits their growth in a dose-dependent manner in vitro with maximal inhibition at an antibody concentration of 1 microg/ml. Different tumor cell lines demonstrate varying sensitivities to anti-betaE11 with the following order of growth inhibition: colon > prostate = glioma > melanoma = fibroblast > breast > liver. Furthermore, the betaE11 antigen localizes to regions of prostatic intraductal neoplasia in paraffin-embedded sections. Mass spectrometry of the cell-derived betaE11 protein and V8-protease fingerprint analysis indicate that the betaE11 antigen is nearly identical to the 4F2 heavy chain antigen, a cell surface protein that has been implicated in cell activation and proliferation. Expression of the betaE11 antigen during mitosis functionally links it to a fundamental aspect of cell proliferation, and its spatial localization on the surface of both proliferating endothelium and tumor cells demonstrates its potential for tumor immunotherapy.
AuthorsM Papetti, I M Herman
JournalThe American journal of pathology (Am J Pathol) Vol. 159 Issue 1 Pg. 165-78 (Jul 2001) ISSN: 0002-9440 [Print] United States
PMID11438464 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antibodies
  • Antigens, CD
  • Antigens, Surface
  • Carrier Proteins
  • Fusion Regulatory Protein-1
  • betaE11 antigen, bovine
Topics
  • Animals
  • Antibodies (pharmacology)
  • Antigens, CD (chemistry, physiology)
  • Antigens, Surface (chemistry, immunology, metabolism)
  • Blotting, Western
  • Carrier Proteins (chemistry, physiology)
  • Cattle
  • Cell Division (drug effects, physiology)
  • Cells, Cultured
  • Endothelium, Vascular (cytology, metabolism)
  • Fusion Regulatory Protein-1
  • Glycosylation
  • Mitosis (physiology)
  • Neoplasms (metabolism, pathology)
  • Protein Processing, Post-Translational
  • Tissue Distribution

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