血管生成
纤维连接蛋白
个性化医疗
癌症研究
细胞外基质
整合素
医学
生物信息学
计算生物学
受体
药理学
生物
细胞生物学
内科学
作者
Samantha Y.A. Terry,Mark Rijpkema,K. Abiraj,Winette T.A. van der Graaf,Wim J.G. Oyen,Otto C. Boerman
标识
DOI:10.2174/13816128113196660665
摘要
Angiogenesis is essential for tumor growth and inhibiting angiogenesis has become an important therapeutic strategy in clinical oncology. Nonetheless, the mechanisms behind anti-angiogenic therapeutics as well as resistance to these drugs remain unclear. With a lack of validated genetic or molecular biomarkers for anti-angiogenic responsiveness, novel methods to identify responsive patients are required. Non-invasive nuclear imaging would allow the elucidation of the basic drug mechanisms as well as resistance routes and aid the personalization of anti-angiogenic therapy by enabling target expression quantification prior to and during treatment. This review focuses on the development of radiolabeled probes to image four key proteins expressed during angiogenesis, namely vascular endothelial growth factor and its receptor, integrin αv β3, the extracellular domain of fibronectin and matrix metalloproteases, and how these probes can be utilized for personalized anti-angiogenic therapy.
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