Angiogenesis and Vascular Targeting in Ewing Sarcoma A Review of Preclinical and Clinical Data

被引:51
作者
DuBois, Steven G. [1 ]
Marina, Neyssa [2 ,3 ]
Glade-Bender, Julia [4 ]
机构
[1] Univ Calif San Francisco, Sch Med, Dept Pediat, San Francisco, CA 94143 USA
[2] Stanford Univ, Sch Med, Dept Pediat, Palo Alto, CA 94304 USA
[3] Lucile Packard Childrens Hosp, Palo Alto, CA USA
[4] Columbia Univ, Sch Med, Morgan Stanley Childrens Hosp, Dept Pediat, New York, NY USA
基金
美国国家卫生研究院;
关键词
angiogenesis; Ewing sarcoma; vascular endothelial growth factor; bevacizumab; thrombospondin; ENDOTHELIAL GROWTH-FACTOR; INITIAL TESTING STAGE-1; PRIMITIVE NEUROECTODERMAL TUMOR; STIMULATES VASCULOGENESIS; PEDIATRIC-PATIENTS; VESSEL FORMATION; PDGF-B; BONE; INHIBITOR; RECEPTOR;
D O I
10.1002/cncr.24844
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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. Cancer 2010;116:749-57. (C) 2009 American Cancer Society.
引用
收藏
页码:749 / 757
页数:9
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