中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
miRNA oligonucleotide and sponge for miRNA-21 inhibition mediated by PEI-PLL in breast cancer therapy

文献类型:期刊论文

作者Li,Mingqiang; Tang,Zhaohui; Zhang,Yu; Lv,Shixian; Li,Quanshun; Chen,Xuesi
刊名acta biomaterialia
出版日期2015
卷号25页码:184-193
关键词CELL LUNG-CANCER DRUG-DELIVERY IN-VIVO CO-DELIVERY ANTITUMOR EFFICACY TUMOR-GROWTH DOXORUBICIN THERAPY PACLITAXEL INHIBITION
通讯作者chen,xs
英文摘要the metastasis of breast cancer is the leading cause of cancer death in women. in this work, an attempt to simultaneously inhibit the primary tumor growth and organ-specific metastasis by the cisplatin-loaded lhrh-modified dextran nanoparticles (dex-sa-cddp-lhrh) was performed in the 4t1 orthotopic mammary tumor metastasis model. with the rationally designed conjugation site of the lhrh ligand, the dex-sa-cddp-lhrh nanoparticles maintained the targeting function of lhrh and specifically bound to the lhrh-receptors overexpressed on the surface of 4t1 breast cancer cells. therefore, the dex-sa-cddp-lhrh nanoparticles exhibited improved cellular uptake and promoted cytotoxicity, when compared with the non-targeted dex-sa-cddp nanoparticles. moreover, both the non-targeted and targeted nanoparticles significantly decreased the systemic toxicity of cddp and increased the maximum tolerated dose of cddp from 4 to 30 mg kg(-1). importantly, dex-sa-cddp-lhrh markedly enhanced the accumulation of cddp in the injected primary tumor and metastasis-containing organs, and meanwhile significantly reduced the nephrotoxicity of cddp. dose-dependent therapeutic effects further demonstrated that the cddp-loaded lhrh-decorated polysaccharide nanoparticles significantly enhanced the antitumor and antimetastasis efficacy, as compared to the non-targeted nanoparticles. these results suggest that dex-sa-cddp-lhrh nanoparticles show great potential for targeted chemotherapy of metastatic breast cancer. (c) 2015 acta materialia inc. published by elsevier ltd. all rights reserved.
收录类别SCI
语种英语
WOS记录号WOS:000361933800018
源URL[http://ir.ciac.jl.cn/handle/322003/64802]  
专题长春应用化学研究所_长春应用化学研究所知识产出_期刊论文
推荐引用方式
GB/T 7714
Li,Mingqiang,Tang,Zhaohui,Zhang,Yu,et al. miRNA oligonucleotide and sponge for miRNA-21 inhibition mediated by PEI-PLL in breast cancer therapy[J]. acta biomaterialia,2015,25:184-193.
APA Li,Mingqiang,Tang,Zhaohui,Zhang,Yu,Lv,Shixian,Li,Quanshun,&Chen,Xuesi.(2015).miRNA oligonucleotide and sponge for miRNA-21 inhibition mediated by PEI-PLL in breast cancer therapy.acta biomaterialia,25,184-193.
MLA Li,Mingqiang,et al."miRNA oligonucleotide and sponge for miRNA-21 inhibition mediated by PEI-PLL in breast cancer therapy".acta biomaterialia 25(2015):184-193.

入库方式: OAI收割

来源:长春应用化学研究所

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