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在细胞膜上原位生成生物相容性的无定形碳酸钙以阻断膜转运蛋白 - 通过模拟异常矿化的癌症治疗新策略。

In situ generation of biocompatible amorphous calcium carbonate onto cell membrane to block membrane transport protein - A new strategy for cancer therapy via mimicking abnormal mineralization.

机构信息

Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Henan Normal University, Xinxiang, Henan 453007, China.

Henan Key Laboratory of Green Chemical Media and Reactions, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007, China.

出版信息

J Colloid Interface Sci. 2019 Apr 1;541:339-347. doi: 10.1016/j.jcis.2019.01.090. Epub 2019 Jan 23.

Abstract

Herein, our aim is to develop a drug-free method without obvious side effects to treat cancer through biomineralization of biocompatible inorganic nanomaterials targeting onto cells' membrane to block transport proteins. We selected chondroitin sulfate as optimal target agent and linker to induce the in situ biomineralization of exogenous Ca and CO at safe concentration to generate biocompatible calcium carbonate (CaCO) nanostructures targeting onto cancer cells' membrane. The in vitro and in vivo assays indicated that the generated CaCO nanostructures could significantly inhibit the proliferation of cancer cells. Mechanism studies demonstrated that the mineralized CaCO nanostructures could bind with 66 membrane proteins. Deeply research revealed that the CaCO nanostructures could mainly block transport proteins, e.g. sodium/potassium-transporting ATPase, leading to the collapse of the mitochondrial membrane potential and the increase of the lactate dehydrogenase release into medium, and finally modulated cell cycle and induced the apoptosis of cancer cells. Our results may introduce promising possibilities for efficient and specific cancer treatment by producing biocompatible nanomaterials to block transport proteins.

摘要

在此,我们的目的是通过靶向细胞膜的生物相容性无机纳米材料的生物矿化来开发一种无明显副作用的、无药物的方法来治疗癌症,以阻断转运蛋白。我们选择硫酸软骨素作为最佳靶向剂和连接子,以在安全浓度下诱导外源性 Ca 和 CO 的原位生物矿化,生成靶向癌细胞膜的生物相容性碳酸钙(CaCO)纳米结构。体外和体内实验表明,所生成的 CaCO 纳米结构可显著抑制癌细胞的增殖。机制研究表明,矿化的 CaCO 纳米结构可以与 66 种膜蛋白结合。深入研究表明,CaCO 纳米结构主要可以阻断转运蛋白,例如钠/钾转运 ATP 酶,导致线粒体膜电位崩溃和乳酸脱氢酶释放到培养基中增加,最终调节细胞周期并诱导癌细胞凋亡。我们的结果可能通过生成生物相容性纳米材料来阻断转运蛋白,为高效和特异性癌症治疗提供了有希望的可能性。

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