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羟基磷灰石纳米球的抗肿瘤作用:激活线粒体依赖性细胞凋亡和负调控磷脂酰肌醇-3-激酶/蛋白激酶 B 通路。

Antitumor Effect by Hydroxyapatite Nanospheres: Activation of Mitochondria-Dependent Apoptosis and Negative Regulation of Phosphatidylinositol-3-Kinase/Protein Kinase B Pathway.

机构信息

National Engineering Research Center for Biomaterials , Sichuan University , Chengdu 610064 , China.

Institute of Atomic and Molecular Physics , Sichuan University , Chengdu 610065 , China.

出版信息

ACS Nano. 2018 Aug 28;12(8):7838-7854. doi: 10.1021/acsnano.8b01996. Epub 2018 Aug 9.

Abstract

Hydroxyapatite nanoparticles (HA NPs) have been acknowledged for their benign biocompatibility and proliferation inhibition effect on tumor cells, attracting considerable attention for tumor therapeutics without late effects. However, unnoticeable tumor cytotoxicity of HA NPs limited the final clinical therapeutic efficacy. Herein, a two-phase synthetic approach was developed to synthesize sphere-like HA NPs by varying the conventional growth habit of HA precipitate. We present our in vitro and in vivo experimental evidence that spherical HA NPs have surprisingly high inhibitory activities against tumor cells. We demonstrate further, based on our experimental data, that the underlying cause for the death of the tumor cells is related to two concurrent pathways, the mitochondria-dependent apoptosis pathway and negative regulation of the phosphatidylinositol-3-kinase/protein kinase B (PIK3/AKT) pathway. The present study indicated that HA nanospheres can be engineered as nontoxic specific inhibitors for efficient tumor therapeutics with nanobiomaterials.

摘要

羟基磷灰石纳米颗粒(HA NPs)因其对肿瘤细胞的良性生物相容性和增殖抑制作用而备受关注,在肿瘤治疗中没有晚期效应,引起了相当大的关注。然而,HA NPs 对肿瘤的不易察觉的细胞毒性限制了最终的临床治疗效果。在此,我们开发了一种两阶段合成方法,通过改变 HA 沉淀物的常规生长习性来合成类球形 HA NPs。我们提供了体外和体内实验证据,表明球形 HA NPs 对肿瘤细胞具有惊人的高抑制活性。我们进一步根据实验数据表明,肿瘤细胞死亡的根本原因与两条同时发生的途径有关,即线粒体依赖性细胞凋亡途径和磷脂酰肌醇-3-激酶/蛋白激酶 B(PIK3/AKT)途径的负调控。本研究表明,HA 纳米球可用作纳米生物材料高效肿瘤治疗的无毒特异性抑制剂。

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