Simultaneous inhibition of metastasis and growth of breast cancer by co-delivery of twist shRNA and paclitaxel using pluronic P85-PEI/TPGS complex nanoparticles
Shen, Jianan2; Sun, Huiping1,2; Xu, Pengfei2; Yin, Qi2; Zhang, Zhiwen2; Wang, Siling1; Yu, Haijun2; Li, Yaping2
刊名BIOMATERIALS
2013-02
卷号34期号:5页码:1581-1590
关键词Metastasis RNA Paclitaxel Twist Pluronic P85
ISSN号0142-9612
DOI10.1016/j.biomaterials.2012.10.057
文献子类Article
英文摘要The metastasis of breast cancer is the leading cause of cancer death in women, and the lung is a common location of a secondary tumor that has metastasized from the primary source tumor. In this work, an attempt to simultaneously inhibit the metastasis and growth of tumor by co-delivering Twist shRNA (shTwi) and paclitaxel (PTX) using the conjugate of pluronic P85 (P85) and low molecular weight polyethyleneimine (PEI) (P85-PEI)/D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS) complex nanoparticles (PTPNs) was performed on metastatic 4T1 breast cancer cell line and its pulmonary metastasis mice model. The experimental results demonstrated that PTPNs could effectively achieve cellular uptake and RNA interference. The down-regulation of Twist protein resulted in significant inhibitory effect of cell migration and invasion with the inhibition rate of 88.7% and 91.06%, respectively. The IC50 of PTPNs against 4T1 cells was 63-fold lower than that of free PTX. The prolonged circulation and increased accumulation of PTX and shTwi in lung and tumor were observed in in vivo biodistribution. The in vivo antitumor efficacy showed that PTPNs could not only inhibit the in situ tumor growth effectively, but also completely restrict the pulmonary metastasis in 4T1 pulmonary metastatic mice model. Therefore, co-delivering chemotherapy drugs with metastasis regulator by PTPNs to simultaneously inhibit metastasis and growth of tumor could achieve synergistic effect for the effective therapy of metastatic breast cancer. (C) 2012 Elsevier Ltd. All rights reserved.
资助项目National Basic Research Program of China[2010CB934000] ; National Basic Research Program of China[2012CB932502] ; National Basic Research Program of China[2009CB930304] ; National Natural Science Foundation of China[30925041] ; National Natural Science Foundation of China[81270047] ; Shanghai Elitist Program[11XD1406200]
WOS关键词MULTIDRUG-RESISTANT CANCER ; OVERCOME DRUG-RESISTANCE ; POLYMERIC MICELLES ; BLOCK-COPOLYMERS ; ANTICANCER DRUG ; SURVIVIN SHRNA ; GENE DELIVERY ; IN-VIVO ; TUMOR ; NANOCARRIERS
WOS研究方向Engineering ; Materials Science
语种英语
出版者ELSEVIER SCI LTD
WOS记录号WOS:000313929400014
内容类型期刊论文
源URL[http://119.78.100.183/handle/2S10ELR8/277753]  
专题药物制剂研究中心
通讯作者Li, Yaping
作者单位1.Shenyang Pharmaceut Univ, Sch Pharm, Shenyang 110016, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China;
推荐引用方式
GB/T 7714
Shen, Jianan,Sun, Huiping,Xu, Pengfei,et al. Simultaneous inhibition of metastasis and growth of breast cancer by co-delivery of twist shRNA and paclitaxel using pluronic P85-PEI/TPGS complex nanoparticles[J]. BIOMATERIALS,2013,34(5):1581-1590.
APA Shen, Jianan.,Sun, Huiping.,Xu, Pengfei.,Yin, Qi.,Zhang, Zhiwen.,...&Li, Yaping.(2013).Simultaneous inhibition of metastasis and growth of breast cancer by co-delivery of twist shRNA and paclitaxel using pluronic P85-PEI/TPGS complex nanoparticles.BIOMATERIALS,34(5),1581-1590.
MLA Shen, Jianan,et al."Simultaneous inhibition of metastasis and growth of breast cancer by co-delivery of twist shRNA and paclitaxel using pluronic P85-PEI/TPGS complex nanoparticles".BIOMATERIALS 34.5(2013):1581-1590.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace