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克服骨肉瘤治疗失败:载有阿帕替尼的疏水性聚(酯酰胺)纳米颗粒

Overcoming therapeutic failure in osteosarcoma Apatinib-encapsulated hydrophobic poly(ester amide) nanoparticles.

作者信息

Li Xiangyu, Wang Liying, Wang Li, Yu Jiaming, Lu Guohao, Zhao Wei, Miao Congxiu, Zou Changye, Wu Jun

机构信息

The Stem Cell and Tissue Engineering Research Center, Changzhi Medical College, Changzhi, Shanxi 046000, P. R. China.

School of Biomedical Engineering, Sun Yat-Sen University, Guangzhou 510006, China.

出版信息

Biomater Sci. 2020 Oct 27;8(21):5888-5899. doi: 10.1039/d0bm01296c.

Abstract

Anti-angiogenic tyrosine kinase inhibitors (TKIs) have been proved to be effective in prolonging progression-free survival in advanced osteosarcoma. However, osteosarcoma stem-like cells persist for a long time and ultimately cause disease recurrence and therapy resistance. Here, we reveal that inefficient accumulation of Apatinib, an anti-angiogenic TKI, induces the expression of ribosome-associated genes in osteosarcoma, and confers apoptosis resistance. An engineered nanoscale delivery system based on hydrophobic poly(ester amide) has been established to effectively deliver Apatinib to improve the treatment. Notably, the considerable uptake by osteosarcoma cells enables this nanodrug to distribute increasingly inside the tumor. Furthermore, the delivered nano-Apatinib can suppress osteosarcoma stemness and enhance osteosarcoma stem-like cell apoptosis, and overcomes the crucial bottleneck of the unfavorable stem-like cell residue for TKI therapy. Importantly, nano-Apatinib significantly inhibits the osteosarcoma stem-like cell-derived tumor growth in contrast with free Apatinib, with minimal side effects. These results suggest that this Apatinib-loaded nano delivery system may serve as a promising strategy to solve the issue of TKI therapeutic resistance existing in advanced osteosarcoma.

摘要

抗血管生成酪氨酸激酶抑制剂(TKIs)已被证明在延长晚期骨肉瘤患者的无进展生存期方面有效。然而,骨肉瘤干细胞样细胞长期存在并最终导致疾病复发和治疗耐药。在此,我们发现抗血管生成TKI阿帕替尼的低效积累会诱导骨肉瘤中核糖体相关基因的表达,并赋予细胞抗凋亡能力。我们建立了一种基于疏水性聚(酯酰胺)的工程化纳米递送系统,以有效递送阿帕替尼来改善治疗效果。值得注意的是,骨肉瘤细胞对该纳米药物的大量摄取使其能够在肿瘤内部实现越来越多的分布。此外,递送的纳米阿帕替尼可以抑制骨肉瘤干性并增强骨肉瘤干细胞样细胞的凋亡,克服了TKI治疗中不利的干细胞样细胞残留这一关键瓶颈。重要的是,与游离阿帕替尼相比,纳米阿帕替尼显著抑制了骨肉瘤干细胞样细胞衍生的肿瘤生长,且副作用极小。这些结果表明,这种负载阿帕替尼的纳米递送系统可能是解决晚期骨肉瘤中存在的TKI治疗耐药问题的一种有前景的策略。

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