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抗血管生成纳米递药系统促进实体瘤中肿瘤血管正常化和微环境重编程。

Anti-angiogenic nano-delivery system promotes tumor vascular normalizing and micro-environment reprogramming in solid tumor.

机构信息

College of Pharmaceutical Science, Zhejiang University, 866 Yuhangtang Road, Hangzhou, 310058, Zhejiang Province, People's Republic of China.

Department of Polymer Science and Engineering, Zhejiang University, 38 Zhe Da Road, Hangzhou 310027, Zhejiang Province, People's Republic of China.

出版信息

J Control Release. 2022 Sep;349:550-564. doi: 10.1016/j.jconrel.2022.07.015. Epub 2022 Jul 21.

Abstract

Aberrant tumor vasculature leads to the malignant tumor microenvironment (TME) for tumor progression. Research has found temporary tumor vascular normalization after treated with low-dose anti-angiogenic agents, however, has paid little attention to prolonging the normalization window and its further influence on tumor tissue. Based on the dose- and time-dependent effect of anti-angiogenic agents, we developed V@LDL NPs, a nano-delivery system sustainedly releasing Vandetanib, an anti-VEGFR2 inhibitor, to control the dose of drug to the normalizing level, and prove its stable tumor vascular normalizing effect in 4 T1 breast cancer model. Furthermore, long-term normalized vasculature could improve tumor perfusion, then provide a circulation to reverse abnormalities in TME, such as hypoxia and heterogeneity, and also inhibit tumor progression. Our findings demonstrate that stable tumor vascular normalization could be a considerable strategy for long-term change to remodel TME and probably result in a therapeutic benefit to anti-cancer treatment, which could be achieved by anti-angiogenic nano-delivery system.

摘要

异常的肿瘤血管导致肿瘤进展的恶性肿瘤微环境(TME)。研究发现,低剂量抗血管生成药物治疗后肿瘤血管短暂正常化,但对延长正常化窗口及其对肿瘤组织的进一步影响关注甚少。基于抗血管生成药物的剂量和时间依赖性效应,我们开发了 V@LDL NPs,一种纳米递药系统,持续释放抗 VEGFR2 抑制剂凡德他尼,将药物剂量控制在正常化水平,并在 4T1 乳腺癌模型中证明其稳定的肿瘤血管正常化作用。此外,长期正常化的血管可以改善肿瘤灌注,从而提供一种循环来逆转 TME 中的异常,如缺氧和异质性,并抑制肿瘤进展。我们的研究结果表明,稳定的肿瘤血管正常化可能是长期改变重塑 TME 的一种可行策略,并且可能对癌症治疗带来治疗益处,这可以通过抗血管生成的纳米递药系统来实现。

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