Abstract

A single intravascular injection of a cyclic peptide or monoclonal antibody antagonist of integrin alpha v beta 3 disrupts ongoing angiogenesis on the chick chorioallantoic membrane (CAM). This leads to the rapid regression of histologically distinct human tumors transplanted onto the CAM. Induction of angiogenesis by a tumor or cytokine promotes vascular cell entry into the cell cycle and expression of integrin alpha v beta 3. After angiogenesis is initiated, antagonists of this integrin induce apoptosis of the proliferative angiogenic vascular cells, leaving preexisting quiescent blood vessels unaffected. We demonstrate therefore that ligation of integrin alpha v beta 3 is required for the survival and maturation of newly forming blood vessels, an event essential for the proliferation of tumors.

Keywords

BiologyAngiogenesisIntegrinChorioallantoic membraneNeovascularizationCancer researchApoptosisCell biologyBlood vesselMonoclonal antibodyImmunologyReceptorEndocrinologyAntibody

MeSH Terms

AllantoisAnimalsApoptosisBlood VesselsChick EmbryoChorionHumansIntegrinsNeoplasm TransplantationNeoplasmsNeovascularizationPathologicReceptorsCytoadhesinReceptorsVitronectinTumor CellsCultured

Affiliated Institutions

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Publication Info

Year
1994
Type
article
Volume
79
Issue
7
Pages
1157-1164
Citations
2268
Access
Closed

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2268
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20
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1850
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Cite This

Peter C. Brooks, Anthony M.P. Montgomery, Mauricio Rosenfeld et al. (1994). Integrin αvβ3 antagonists promote tumor regression by inducing apoptosis of angiogenic blood vessels. Cell , 79 (7) , 1157-1164. https://doi.org/10.1016/0092-8674(94)90007-8

Identifiers

DOI
10.1016/0092-8674(94)90007-8
PMID
7528107

Data Quality

Data completeness: 81%