Monitoring response to anticancer therapy by targeting microbubbles to tumor vasculature

被引:209
|
作者
Korpanty, Grzegorz
Carbon, Juliet G.
Grayburn, Paul A.
Fleming, Jason B.
Brekken, Rolf A.
机构
[1] Univ Texas, SW Med Ctr, Hamon Ctr Therapeut Oncol Res, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Surg, Dallas, TX 75390 USA
[3] Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA
[4] Baylor Univ, Med Ctr, Baylor Heart & Vasc Inst, Dallas, TX USA
关键词
D O I
10.1158/1078-0432.CCR-06-1313
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: New strategies to detect tumor angiogenesis and monitor response of tumor vasculature to therapy are needed. Contrast ultrasound imaging using microbubbles targeted to tumor endothelium offers a noninvasive method for monitoring and quantifying vascular effects of antitumor therapy. We investigated the use of targeted microbubbles to follow vascular response of therapy in a mouse model of pancreatic adenocarcinoma. Experimental Design: Microbubbles conjugated to monoclonal antibodies were used to image and quantify vascular effects of two different antitumor therapies in s.c. and orthotopic pancreatic tumors in mice. Tumor-bearing mice were treated with anti-vascular endothelial growth factor (VEGF) monoclonal antibodies and/or gemcitabine, and the localization of microbubbles to endoglin (CD105), VEGF receptor 2 (VEGFR2), or VEGF-activated blood vessels (the VEGF-VEGFR complex) was monitored by contrast ultrasound. Results: Targeted microbubbles showed significant enhancement of tumor vasculature when compared with untargeted or control IgG-targeted microbubbles. Video intensity from targeted microbubbles correlated with the level of expression of the target (CD105,VEGFR2, or the VEGF-VEGFR complex) and with microvessel density in tumors under antiangiogenic or cytotoxic therapy. Conclusions: We conclude that targeted microbubbles represent a novel and attractive tool for noninvasive, vascular-targeted molecular imaging of tumor angiogenesis and for monitoring vascular effects specific to antitumor therapy in vivo.
引用
收藏
页码:323 / 330
页数:8
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