Affiliation:
1. From the Center for Biologics Evaluation and Research, Rockville, Maryland 20852; and the Laboratory of Cell Biology, the Laboratory of Pathology, and the Laboratory of Experimental Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892
Abstract
An endothelial cell inhibitor was purified from supernatant of an Epstein-Barr virus–immortalized cell line and identified as fragments of calreticulin. The purified recombinant NH2-terminal domain of calreticulin (amino acids 1–180) inhibited the proliferation of endothelial cells, but not cells of other lineages, and suppressed angiogenesis in vivo. We have named this NH2-terminal domain of calreticulin vasostatin. When inoculated into athymic mice, vasostatin significantly reduced growth of human Burkitt lymphoma and human colon carcinoma. Compared with other inhibitors of angiogenesis, vasostatin is a small, soluble, and stable molecule that is easy to produce and deliver. As an angiogenesis inhibitor that specifically targets proliferating endothelial cells, vasostatin has a unique potential for cancer treatment.
Publisher
Rockefeller University Press
Subject
Immunology,Immunology and Allergy
Cited by
268 articles.
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