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Updated: Jul 23, 2026

Monitoring Functionality and Morphology of Vasculature Recruited by Factors Secreted by Fast-growing Tumor-generating Cells
Published on: November 23, 2014
Role of Id proteins in embryonic and tumor angiogenesis
1Cell Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA. r-benezra@ski.mskcc.org
Abstract:
It has been shown recently in mouse model systems that the Id proteins play a critical role in angiogenesis both during embryogenesis and tumor formation. The Id proteins are intracellular proteins that inhibit the activity of differentiation-promoting transcription factors and thereby block differentiation and promote cell cycle progression. Loss of Id function in mice leads to premature neural differentiation and withdrawal from the cell cycle in neurons and also the execution of an aberrant differentiation cascade in endothelial cells. This latter event is associated with a mid-gestational brain hemorrhage when Id dosage is sufficiently low. Partial reduction in Id levels spares the endothelium in the brain but adults born fail to support the vascularization of tumors. Through the analysis of these phenotypes and characterization of altered gene expression in the Id knockout endothelium, subdivisions in the angiogenic process are being defined which may lead to selective anti-angiogenic treatments in the management of human disease.
Insights
Id proteins are crucial for blood vessel formation (angiogenesis) in mice, impacting development and tumor growth. Their loss causes developmental defects and impairs tumor vascularization, suggesting new anti-angiogenic treatment targets.
Area of Science:
- Developmental Biology
- Molecular Biology
- Oncology
Background:
- Id proteins are intracellular regulators that inhibit differentiation-promoting transcription factors.
- Id proteins play a critical role in angiogenesis during embryogenesis and tumor formation.
- Loss of Id function in mouse models leads to aberrant differentiation in neurons and endothelial cells.
Purpose of the Study:
- To investigate the role of Id proteins in angiogenesis during embryogenesis and tumor formation.
- To define subdivisions in the angiogenic process through analysis of Id knockout phenotypes.
- To identify potential targets for selective anti-angiogenic therapies.
Main Methods:
- Analysis of Id knockout mouse models.
- Characterization of gene expression in Id knockout endothelium.
- Phenotypic analysis of developmental and tumor vascularization defects.
Main Results:
- Loss of Id function causes premature neural differentiation and mid-gestational brain hemorrhage in mice.
- Reduced Id levels impair the ability of adult mice to support tumor vascularization.
- Specific defects in the angiogenic process were identified in Id-deficient endothelium.
Conclusions:
- Id proteins are essential for normal angiogenesis and vascular development.
- Understanding Id protein function provides insights into selective anti-angiogenic strategies.
- Targeting Id proteins may offer novel therapeutic approaches for cancer and other diseases.
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