Zhang Bo, Jiang Ting, Tuo Yanyan, Jin Kai, Luo Zimiao, Shi Wei, Mei Heng, Hu Yu, Pang Zhiqing, Jiang Xinguo
Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
School of Pharmacy, Fudan University, Key Laboratory of Smart Drug Delivery, Ministry of Education, 826 Zhangheng Road, Shanghai, 201203, PR China.
Cancer Lett. 2017 Dec 1;410:12-19. doi: 10.1016/j.canlet.2017.09.007. Epub 2017 Sep 20.
Poor tumor perfusion and unfavorable vessel permeability compromise nanomedicine drug delivery to tumors. Captopril dilates blood vessels, reducing blood pressure clinically and bradykinin, as the downstream signaling moiety of captopril, is capable of dilating blood vessels and effectively increasing vessel permeability. The hypothesis behind this study was that captopril can dilate tumor blood vessels, improving tumor perfusion and simultaneously enlarge the endothelial gaps of tumor vessels, therefore enhancing nanomedicine drug delivery for tumor therapy. Using the U87 tumor xenograft with abundant blood vessels as the tumor model, tumor perfusion experiments were carried out using laser Doppler imaging and lectin-labeling experiments. A single treatment of captopril at a dose of 100 mg/kg significantly increased the percentage of functional vessels in tumor tissues and improved tumor blood perfusion. Scanning electron microscopy of tumor vessels also indicated that the endothelial gaps of tumor vessels were enlarged after captopril treatment. Immunofluorescence-staining of tumor slices demonstrated that captopril significantly increased bradykinin expression, possibly explaining tumor perfusion improvements and endothelial gap enlargement. Additionally, imaging in vivo, imaging ex vivo and nanoparticle distribution in tumor slices indicated that after a single treatment with captopril, the accumulation of 115-nm nanoparticles in tumors had increased 2.81-fold with a more homogeneous distribution pattern in comparison to non-captopril treated controls. Finally, pharmacodynamics experiments demonstrated that captopril combined with paclitaxel-loaded nanoparticles resulted in the greatest tumor shrinkage and the most extensive necrosis in tumor tissues among all treatment groups. Taken together, the data from the present study suggest a novel strategy for improving tumor perfusion and enlarging blood vessel permeability simultaneously in order to improve nanomedicine delivery for tumor therapy. As captopril has already been extensively used clinically, such a strategy has great therapeutic potential.
肿瘤灌注不良和血管通透性不佳会影响纳米药物向肿瘤的递送。卡托普利可扩张血管,临床上能降低血压,而作为卡托普利下游信号部分的缓激肽能够扩张血管并有效增加血管通透性。本研究背后的假设是,卡托普利可扩张肿瘤血管,改善肿瘤灌注,同时扩大肿瘤血管的内皮间隙,从而增强纳米药物用于肿瘤治疗的递送效果。以血管丰富的U87肿瘤异种移植模型为研究对象,采用激光多普勒成像进行肿瘤灌注实验,并进行凝集素标记实验。单次给予100mg/kg剂量的卡托普利可显著增加肿瘤组织中功能性血管的比例,改善肿瘤血液灌注。肿瘤血管的扫描电子显微镜检查也表明,卡托普利治疗后肿瘤血管的内皮间隙增大。肿瘤切片的免疫荧光染色显示,卡托普利显著增加了缓激肽的表达,这可能解释了肿瘤灌注的改善和内皮间隙的扩大。此外,体内成像、体外成像以及肿瘤切片中的纳米颗粒分布表明,单次给予卡托普利后,与未用卡托普利治疗的对照组相比,115nm纳米颗粒在肿瘤中的蓄积增加了2.81倍,且分布模式更均匀。最后,药效学实验表明,在所有治疗组中,卡托普利与载有紫杉醇的纳米颗粒联合使用导致肿瘤缩小最大,肿瘤组织坏死范围最广。综上所述,本研究数据提示了一种同时改善肿瘤灌注和扩大血管通透性以提高纳米药物用于肿瘤治疗递送效果的新策略。由于卡托普利已在临床上广泛应用,这种策略具有巨大的治疗潜力。