pH-Sensitive Nano-Complexes Overcome Drug Resistance and Inhibit Metastasis of Breast Cancer by Silencing Akt Expression
Yin, Jieying1,2,3; Lang, Tianqun1,2,4; Cun, Dongmei3; Zheng, Zhong1,2; Huang, Yan1,2,3; Yin, Qi1,2; Yu, Haijun1,2; Li, Yaping1,2
刊名THERANOSTICS
2017
卷号7期号:17页码:4204-4216
ISSN号1838-7640
DOI10.7150/thno.21516
文献子类Article
英文摘要The therapy of breast cancer is encumbered by drug resistance and metastasis, which can be due to a defective PI3K/AKT/mTOR signaling pathway. This study was aimed at improving the anti-cancer effect of the chemotherapeutic agent paclitaxel (PTX) on the drug resistant and metastatic breast cancer by co-delivering PTX and a siRNA, siAkt, directed at silencing the Akt expression. Methods: The pH-sensitive amphiphilic polymer, poly [(1,4-butanediol)-diacrylate-beta-N, N-diisopropylethylenediamine]-polyethyleneimine (BDP) was synthesized. The PTX-loaded BDP micelle/siAkt nano-complex (PMA) was prepared and characterized. The cellular uptake, cytotoxicity, RNA interference efficiency, biodistribution, pharmacokinetics, pharmacodynamics, and biocompatibility of PMA in the murine metastatic breast cancer 4T1 cells and the 4T1 tumor-bearing mice were evaluated. Results: PMA was stable at the neutral as well as tumor extracellular pH and released the drugs in the intra-endo/lysosome acidic environment. In 4T1 cells, the RNA interference against the Akt gene down-regulated the expression of Akt and P-glycoprotein and up-regulated the expression of Caspase-3. The down-regulated P-gp inhibits the efflux of PTX thereby increasing its intracellular concentration, improving the cytotoxicity, and inhibiting the migration and invasion of 4T1 cells. In the 4T1 tumor-bearing mice, co-delivery of PTX and siAkt by PMA achieved a tumor inhibiting rate of 94.1% and suppressed 96.8% lung metastases. PMA did not cause pathological lesions in normal organs. Conclusion: PMA, by virtue of overcoming drug resistance and simultaneously restraining lung metastasis, might be an efficient drug delivery system for the therapy of breast cancer.
资助项目National Basic Research Program of China[2014CB931900] ; National Natural Science Foundation of China[81690265] ; National Natural Science Foundation of China[81521005] ; Youth Innovation Promotion Association of CAS[2015226]
WOS关键词SIRNA DELIVERY ; TUMOR-METASTASIS ; THERAPY ; HETEROGENEITY ; THERAPEUTICS ; DESIGN
WOS研究方向Research & Experimental Medicine
语种英语
出版者IVYSPRING INT PUBL
WOS记录号WOS:000412296800010
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/275697]  
专题药物制剂研究中心
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Yin, Qi; Li, Yaping
作者单位1.Chinese Acad Sci, State Key Lab Drug Res, Shanghai 201203, Peoples R China;
2.Chinese Acad Sci, Ctr Pharmaceut, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China;
3.Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Liaoning, Peoples R China;
4.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
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GB/T 7714
Yin, Jieying,Lang, Tianqun,Cun, Dongmei,et al. pH-Sensitive Nano-Complexes Overcome Drug Resistance and Inhibit Metastasis of Breast Cancer by Silencing Akt Expression[J]. THERANOSTICS,2017,7(17):4204-4216.
APA Yin, Jieying.,Lang, Tianqun.,Cun, Dongmei.,Zheng, Zhong.,Huang, Yan.,...&Li, Yaping.(2017).pH-Sensitive Nano-Complexes Overcome Drug Resistance and Inhibit Metastasis of Breast Cancer by Silencing Akt Expression.THERANOSTICS,7(17),4204-4216.
MLA Yin, Jieying,et al."pH-Sensitive Nano-Complexes Overcome Drug Resistance and Inhibit Metastasis of Breast Cancer by Silencing Akt Expression".THERANOSTICS 7.17(2017):4204-4216.
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