Vascular normalization as a therapeutic strategy for malignant and nonmalignant disease
Shom Goel1, Andus Hon-Kit Wong, Rakesh K Jain
1Edwin Steele Laboratory for Tumor Biology, Department of Radiation Oncology, Massachusetts General Hospital, Boston, Massachusetts 02114, USA. jain@steele.mgh.harvard.edu
Pathological angiogenesis causes abnormal new blood vessels in diseases. Antiangiogenic therapy can normalize this vasculature, improving treatments for tumors and benign conditions.
Area of Science:
- Vascular Biology and Medicine
- Oncology
- Pathology
Background:
- Pathological angiogenesis, driven by disrupted signaling, leads to immature and abnormal vasculature in diseases.
- This aberrant microvasculature promotes disease progression and hinders treatment efficacy.
- Understanding this imbalance is crucial for developing effective therapies.
Purpose of the Study:
- To introduce and support the "vascular normalization" hypothesis.
- To demonstrate how restoring angiogenic balance can normalize pathological vasculature.
- To review evidence for antiangiogenic therapy in treating diseases.
Main Methods:
- Review of preclinical studies on antiangiogenic therapy.
- Analysis of clinical trial data for solid tumors and benign conditions.
- Examination of molecular and structural changes in diseased vasculature.
Main Results:
- Preclinical and clinical evidence supports the vascular normalization hypothesis.
- Antiangiogenic therapy can restore a more normal vascular structure and function.
- This normalization contributes to successful treatment outcomes.
Conclusions:
- The vascular normalization hypothesis provides a framework for understanding antiangiogenic therapy.
- Targeting angiogenic signaling can normalize pathological vasculature in various diseases.
- This approach has shown promise in treating both malignant and benign conditions.
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