Karimi Hanieh, Lee Sarah, Xu Wenqi, Langhans Sigrid A, Johnson David K, Stauff Erik, Kecskemethy Heidi H, Averill Lauren W, Yue Xuyi
Department of Radiology, Diagnostic and Research PET/MR Center, Nemours Children's Health, Wilmington, DE 19803, USA.
Diagnostic & Research PET/MR Center, Nemours Children's Health, Delaware, Wilmington, DE 19803, USA.
Int J Mol Sci. 2025 Jun 4;26(11):5373. doi: 10.3390/ijms26115373.
Vascular endothelial growth factor receptors (VEGFRs) are key regulators of angiogenesis, lymphangiogenesis, and vascular permeability, playing essential roles in both physiological and pathological processes. The VEGFR family, including VEGFR-1, VEGFR-2, and VEGFR-3, interacts with structurally related VEGF ligands (VEGFA, VEGFB, VEGFC, VEGFD, and placental growth factor [PlGF]), activating downstream signaling pathways that mediate critical cellular processes, including proliferation, migration, and survival. Dysregulation of VEGFR signaling has been implicated in numerous diseases, such as cancer, cardiovascular conditions, and inflammatory disorders. Targeting VEGFRs with radiopharmaceuticals, such as radiolabeled peptides, antibodies, and specific tracers like Cu-bevacizumab and Zr-ramucirumab, has emerged as a powerful strategy for non-invasive imaging of VEGFR expression and distribution in vivo. Through positron emission tomography (PET) and single-photon emission computed tomography (SPECT), these targeted tracers enable real-time visualization of angiogenic and lymphangiogenic activity, providing insights into disease progression and therapeutic responses. This review explores the current advances in VEGFR-targeted imaging, focusing on the development of novel tracers, radiolabeling techniques, and their in vivo imaging characteristics. We discuss the preclinical and clinical applications of VEGFR imaging, highlight existing challenges, and provide perspectives on future innovations that could further enhance precision diagnostics and therapeutic monitoring in angiogenesis and lymphangiogenesis-driven diseases.
血管内皮生长因子受体(VEGFRs)是血管生成、淋巴管生成和血管通透性的关键调节因子,在生理和病理过程中均发挥着重要作用。VEGFR家族包括VEGFR-1、VEGFR-2和VEGFR-3,与结构相关的VEGF配体(VEGFA、VEGFB、VEGFC、VEGFD和胎盘生长因子[PlGF])相互作用,激活介导关键细胞过程(包括增殖、迁移和存活)的下游信号通路。VEGFR信号失调与多种疾病有关,如癌症、心血管疾病和炎症性疾病。用放射性药物靶向VEGFRs,如放射性标记的肽、抗体以及特定示踪剂(如铜标记的贝伐单抗和锆标记的雷莫西尤单抗),已成为一种用于体内VEGFR表达和分布无创成像的有力策略。通过正电子发射断层扫描(PET)和单光子发射计算机断层扫描(SPECT),这些靶向示踪剂能够实时可视化血管生成和淋巴管生成活动,为疾病进展和治疗反应提供见解。本综述探讨了VEGFR靶向成像的当前进展,重点关注新型示踪剂的开发、放射性标记技术及其体内成像特征。我们讨论了VEGFR成像的临床前和临床应用,强调了现有挑战,并对未来的创新提供了展望,这些创新可能会进一步提高血管生成和淋巴管生成驱动疾病的精确诊断和治疗监测水平。