中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A distinct endocytic mechanism of functionalized-silica nanoparticles in breast cancer stem cells

文献类型:期刊论文

作者Sun, Jiadong1,2,3; Liu, Yajing1,2; Ge, Min1,2; Zhou, Guoqiang1,2; Sun, Wentong1,2; Liu, Dandan1,2; Liang, Xing-Jie3; Zhang, Jinchao1,2
刊名Scientific reports
出版日期2017-11-24
卷号7页码:13
ISSN号2045-2322
DOI10.1038/s41598-017-16591-z
通讯作者Liu, dandan(leo-liudan@163.com) ; Liang, xing-jie(liangxj@nanoctr.cn) ; Zhang, jinchao(jczhang6970@163.com)
英文摘要Nanoparticles provide new fields for life medical science application, including targeted-drug delivery and cancer treatment. to maximize the delivery efficiency of nanoparticle, one must understand the uptake mechanism of nanoparticle in cells, which may determine their ultimate fate and localization in cells. recently, the proposed-cancer stem cell (csc) theory has been attracted great attention and regarded as new targets for the new nanodrug developmet and cancer therapies. the interaction between nanoparticles and cancer cells has been extensively studied, but the uptake mechanism of nanoparticles in cscs has received little attention. here, we use the pharmacological inhibitors of major endocytic pathways to study the silica nanoparticle (sinp) uptake mechanisms in the human breast adenocarcinoma cell line (mcf-7) and mcf-7-derived breast cancer stem cells (bcscs). the results demonstrate that the uptake of sinps, particularly amino-functionalized sinps, in mcf-7 cells is strongly affected by the actin depolymerization, whereas bcscs more strongly inhibit the amino-functionalized sinp uptake after the scavenger receptor disruption. these findings indicate a distinct endocytic mechanism of functionalized sinps in bcscs, which is significant for designing ideal nanosized drug delivery systems and improving the selectivity for csc-targeted therapy.
WOS关键词CLATHRIN-INDEPENDENT ENDOCYTOSIS ; SURFACE-CHARGE ; ACTIN POLYMERIZATION ; EPITHELIAL-CELLS ; MAMMALIAN-CELLS ; DELIVERY-SYSTEM ; CELLULAR UPTAKE ; DRUG-DELIVERY ; GENE DELIVERY ; INTERNALIZATION
WOS研究方向Science & Technology - Other Topics
WOS类目Multidisciplinary Sciences
语种英语
WOS记录号WOS:000416135000035
出版者NATURE PUBLISHING GROUP
URI标识http://www.irgrid.ac.cn/handle/1471x/2177796
专题高能物理研究所
通讯作者Liu, Dandan; Liang, Xing-Jie; Zhang, Jinchao
作者单位1.Hebei Univ, Key Lab Med Chem & Mol Diag, Minist Educ, Baoding 071002, Peoples R China
2.Hebei Univ, Coll Chem & Environm Sci, Chem Biol Key Lab Hebei Prov, Baoding 071002, Peoples R China
3.Natl Ctr Nanosci & Technol, CAS Key Lab Biol Effects Nanomat & Nanosafety, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Sun, Jiadong,Liu, Yajing,Ge, Min,et al. A distinct endocytic mechanism of functionalized-silica nanoparticles in breast cancer stem cells[J]. Scientific reports,2017,7:13.
APA Sun, Jiadong.,Liu, Yajing.,Ge, Min.,Zhou, Guoqiang.,Sun, Wentong.,...&Zhang, Jinchao.(2017).A distinct endocytic mechanism of functionalized-silica nanoparticles in breast cancer stem cells.Scientific reports,7,13.
MLA Sun, Jiadong,et al."A distinct endocytic mechanism of functionalized-silica nanoparticles in breast cancer stem cells".Scientific reports 7(2017):13.

入库方式: iSwitch采集

来源:高能物理研究所

浏览0
下载0
收藏0
其他版本

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。