Niu Gang, Chen Xiaoyuan
PET Clin. 2009 Jan 1;4(1):17-38. doi: 10.1016/j.cpet.2009.04.011.
Angiogenesis is a highly-controlled process that is dependent on the intricate balance of both promoting and inhibiting factors, involved in various physiological and pathological processes. A comprehensive understanding of the molecular mechanisms that regulate angiogenesis has resulted in the design of new and more effective therapeutic strategies. Due to insufficient sensitivity to detect therapeutic effects by using standard clinical endpoints or by looking for physiological improvement, a multitude of imaging techniques have been developed to assess tissue vasculature on the structural, functional and molecular level. Imaging is expected to provide a novel approach to noninvasively monitor angiogenesis, to optimize the dose of new antiangiogenic agents and to assess the efficacy of therapies directed at modulation of the angiogenic process. All these methods have been successfully used preclinically and will hopefully aid in antiangiogenic drug development in animal studies. In this review article, the application of PET in angiogenesis imaging at both functional and molecular level will be discussed. For PET imaging of angiogenesis related molecular markers, we emphasize integrin alpha(v)beta(3), VEGF/VEGFR, and MMPs.
血管生成是一个高度受控的过程,它依赖于促进和抑制因子的复杂平衡,涉及各种生理和病理过程。对调节血管生成的分子机制的全面理解导致了新的、更有效的治疗策略的设计。由于使用标准临床终点或寻找生理改善来检测治疗效果的敏感性不足,已经开发了多种成像技术来在结构、功能和分子水平上评估组织脉管系统。成像有望提供一种非侵入性监测血管生成的新方法,以优化新型抗血管生成药物的剂量,并评估针对调节血管生成过程的疗法的疗效。所有这些方法已在临床前成功应用,有望在动物研究中辅助抗血管生成药物的开发。在这篇综述文章中,将讨论PET在功能和分子水平的血管生成成像中的应用。对于血管生成相关分子标志物的PET成像,我们重点介绍整合素α(v)β(3)、VEGF/VEGFR和基质金属蛋白酶。