首页> 外文期刊>Antioxidants and redox signalling >In vivo imaging of tumor physiological, metabolic, and redox changes in response to the anti-angiogenic agent sunitinib: Longitudinal assessment to identify transient vascular renormalization
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In vivo imaging of tumor physiological, metabolic, and redox changes in response to the anti-angiogenic agent sunitinib: Longitudinal assessment to identify transient vascular renormalization

机译:体内成像对响应抗血管生成剂舒尼替尼的肿瘤生理,代谢和氧化还原变化的影响:纵向评估以鉴定短暂性血管再正常化

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Aims: The tumor microenvironment is characterized by a highly reducing redox status, a low pH, and hypoxia. Anti-angiogenic therapies for solid tumors frequently function in two steps: the transient normalization of structurally and functionally aberrant tumor blood vessels with increased blood perfusion, followed by the pruning of tumor blood vessels and the resultant cessation of nutrients and oxygen delivery required for tumor growth. Conventional anatomic or vascular imaging is impractical or insufficient to distinguish between the two steps of tumor response to anti-angiogenic therapies. Here, we investigated whether the noninvasive imaging of the tumor redox state and energy metabolism could be used to characterize anti-angiogenic drug-induced transient vascular normalization. Results: Daily treatment of squamous cell carcinoma (SCCVII) tumor-bearing mice with the multi-tyrosine kinase inhibitor sunitinib resulted in a rapid decrease in tumor microvessel density and the suppression of tumor growth. Tumor pO2 imaging by electron paramagnetic resonance imaging showed a transient increase in tumor oxygenation after 2-4 days of sunitinib treatment, implying improved tumor perfusion. During this window of vascular normalization, magnetic resonance imaging of the redox status using an exogenously administered nitroxide probe and hyperpolarized 13C MRI of the metabolic flux of pyruvate/lactate couple revealed an oxidative shift in tumor redox status. Innovation: Redox-sensitive metabolic couples can serve as noninvasive surrogate markers to identify the vascular normalization window in tumors with imaging techniques. Conclusion: A multimodal imaging approach to characterize physiological, metabolic, and redox changes in tumors is useful to distinguish between the different stages of anti-angiogenic treatment. Antioxid. Redox Signal. 21, 1145-1155.
机译:目的:肿瘤微环境的特征是氧化还原状态高度降低,pH值低和缺氧。实体瘤的抗血管生成疗法通常分两个步骤发挥作用:结构和功能异常的肿瘤血管的短暂正常化,血液灌注增加,随后肿瘤血管的修剪以及随之而来的肿瘤生长所需的营养和氧气输送的停止。传统的解剖或血管成像是不切实际的或不足以区分肿瘤对抗血管生成疗法的反应的两个步骤。在这里,我们调查了肿瘤氧化还原状态和能量代谢的无创成像是否可用于表征抗血管生成药物诱导的瞬时血管正常化。结果:每天用多酪氨酸激酶抑制剂舒尼替尼治疗鳞状细胞癌(SCCVII)荷瘤小鼠会导致肿瘤微血管密度迅速降低并抑制肿瘤生长。通过电子顺磁共振成像进行的肿瘤pO2成像显示,舒尼替尼治疗2-4天后,肿瘤氧合的瞬时增加,表明肿瘤灌注得到改善。在该血管正常化窗口期间,使用外源性给予的一氧化氮探针对丙酮酸/乳酸盐对的代谢通量进行超极化的13C MRI磁共振成像对氧化还原状态的成像显示出肿瘤氧化还原状态的氧化位移。创新:氧化还原敏感的代谢对可以作为非侵入性替代标志物,通过成像技术识别肿瘤中的血管正常化窗口。结论:表征肿瘤生理,代谢和氧化还原变化的多峰成像方法可用于区分抗血管生成治疗的不同阶段。抗氧化。氧化还原信号。 21,1145-1155。

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