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Published on: December 9, 2016
Angiogenesis and vascular targeting in Ewing sarcoma: a review of preclinical and clinical data
Steven G DuBois1, Neyssa Marina, Julia Glade-Bender
1Department of Pediatrics, University of California at San Francisco School of Medicine, San Francisco, California 94143-0106, USA. duboiss@peds.ucsf.edu
Abstract:
Ewing sarcoma is the second most common type of bone cancer in children and young adults. In recent years, the mechanisms by which these tumors develop and maintain their vascular supply have been elucidated. Additional work has demonstrated that inhibition of angiogenic pathways or disruption of established vasculature can attenuate the growth of Ewing sarcoma mouse xenografts. Early clinical data suggest that these results also may extend to patients with Ewing sarcoma who are treated with antiangiogenic or antivascular therapies. For the current review, the authors summarized the available data supporting this approach.
Insights
Researchers reviewed data on targeting blood vessel growth in Ewing sarcoma. Inhibiting tumor vascularization shows promise in slowing cancer growth in preclinical models and potentially in patients.
Area of Science:
- Pediatric Oncology
- Cancer Biology
- Tumor Angiogenesis
Background:
- Ewing sarcoma is a prevalent bone cancer in pediatric and young adult populations.
- Understanding tumor vascularization mechanisms is crucial for developing effective treatments.
- Previous research highlighted the role of angiogenesis in Ewing sarcoma progression.
Purpose of the Study:
- To review current data supporting anti-angiogenic and anti-vascular therapies for Ewing sarcoma.
- To summarize the efficacy of targeting tumor vasculature in preclinical and clinical settings.
Main Methods:
- Literature review of studies investigating Ewing sarcoma and its vascular supply.
- Analysis of preclinical data from mouse xenograft models.
- Evaluation of early clinical trial results for anti-angiogenic/anti-vascular therapies.
Main Results:
- Inhibition of angiogenic pathways can reduce Ewing sarcoma xenograft growth.
- Disruption of established tumor vasculature also attenuates tumor progression.
- Preliminary clinical data suggest potential benefits of these therapies in patients.
Conclusions:
- Targeting tumor angiogenesis and vasculature is a viable therapeutic strategy for Ewing sarcoma.
- Further clinical investigation is warranted to confirm the efficacy of anti-angiogenic and anti-vascular treatments.
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