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多西他赛和萝卜硫素负载的自组装聚(D,L-丙交酯-共-乙交酯)/透明质酸嵌段共聚物纳米颗粒联合靶向分化型乳腺癌细胞和乳腺癌干细胞

Simultaneous Targeting of Differentiated Breast Cancer Cells and Breast Cancer Stem Cells by Combination of Docetaxel- and Sulforaphane-Loaded Self-Assembled Poly(D, L-lactide-co-glycolide)/Hyaluronic Acid Block Copolymer-Based Nanoparticles.

作者信息

Huang Jingbin, Tao Chun, Yu Yuan, Yu Feifei, Zhang He, Gao Jie, Wang Dong, Chen Yan, Gao Jing, Zhang Guoqing, Zhou Guichen, Liu Junjie, Sun Zhiguo, Sun Duxin, Zou Hao, Xu Hao, Lu Ying, Zhong Yanqiang

出版信息

J Biomed Nanotechnol. 2016 Jul;12(7):1463-77. doi: 10.1166/jbn.2016.2234.

Abstract

Breast cancer stem cells (BCSCs) are implicated in the initiation and progression of breast cancer and are responsible for metastasis and recurrence. In this study, we attempted to simultaneously target differentiated breast cancer cells (DBCCs) and BCSCs by using a combination of docetaxel (DTX)- and sulforaphane (SFN)-loaded poly(D, L-lactide-coglycolide)/hyaluronic acid (PLGA-b-HA)-based nanoparticles. BCSCs were identified as having an ESA+CD44+CD24– phenotype, which exhibited docetaxel resistance. Drug-loaded nanoparticles exhibited enhanced cytotoxicity towards both DBCCs and BCSCs compared with free drugs. SFN-loaded nanoparticles were more effective in inhibiting BCSCs than free SFN in vitro by down-regulating β-catenin expression. In vivo analysis of anti-tumor activity showed that the combination therapy with DTX- and SFN-loaded nanoparticles had the strongest antitumor efficacy. In vivo analysis of anti-BCSCs activity showed that the self-renewal ability of BCSCs was strongly inhibited in DTX- and SFN-loaded nanoparticle-treated groups. In conclusion, the combination of SFN- and DTX-loaded PLGA-b-HA nanoparticles shows therapeutic potential in the treatment of breast cancer by simultaneously targeting DBCCs and BCSCs.

摘要

乳腺癌干细胞(BCSCs)与乳腺癌的发生和发展有关,并且是转移和复发的原因。在本研究中,我们试图通过使用载有多西他赛(DTX)和萝卜硫素(SFN)的聚(D,L-丙交酯-共乙交酯)/透明质酸(PLGA-b-HA)纳米颗粒同时靶向分化型乳腺癌细胞(DBCCs)和BCSCs。BCSCs被鉴定为具有ESA+CD44+CD24–表型,其表现出对多西他赛的抗性。与游离药物相比,载药纳米颗粒对DBCCs和BCSCs均表现出增强的细胞毒性。载有SFN的纳米颗粒在体外通过下调β-连环蛋白表达比游离SFN更有效地抑制BCSCs。抗肿瘤活性的体内分析表明,载有DTX和SFN的纳米颗粒联合治疗具有最强的抗肿瘤功效。抗BCSCs活性的体内分析表明,在载有DTX和SFN的纳米颗粒处理组中,BCSCs的自我更新能力受到强烈抑制。总之,载有SFN和DTX的PLGA-b-HA纳米颗粒的组合通过同时靶向DBCCs和BCSCs在乳腺癌治疗中显示出治疗潜力。

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