中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Overcoming resistance to cisplatin by inhibition of glutathione s-transferases (gsts) with ethacraplatin micelles in vitro and in vivo

文献类型:期刊论文

作者Li, Shuyi1,2; Li, Chan1,2; Jin, Shubin3; Liu, Juan4; Xue, Xiangdong1; Eltahan, Ahmed Shaker1,2; Sun, Jiadong1; Tan, Jingjie1; Dong, Jinchen1; Liang, Xing-Jie1,2
刊名Biomaterials
出版日期2017-11-01
卷号144页码:119-129
关键词Cisplatin resistance Glutathione s-transferases (gsts) Ethacraplatin Drug delivery
ISSN号0142-9612
DOI10.1016/j.biomaterials.2017.08.021
通讯作者Li, chan(lic@nanoctr.cn) ; Liang, xing-jie(liangxj@nanoctr.cn)
英文摘要Platinum-based dna-adducting agents are used extensively in the clinic for cancer chemotherapy. however, the anti-tumor efficacy of these drugs is severely limited by cisplatin resistance, and this can lead to the failure of chemotherapy. one of cisplatin resistance mechanisms is associated with over expression of glutathione s-transferases (gsts), which would accelerate the deactivation of cisplatin and decrease its antitumor efficiency. nanoscale micelles encapsulating ethacraplatin, a conjugate of cisplatin and ethacrynic acid (an effective gsts inhibitor), can enhance the accumulation of active cisplatin in cancer cells by inhibiting the activity of gsts and circumventing deactivation of cisplatin. in vitro and in vivo results provide strong evidence that gsts inhibitor-modified cisplatin prodrug combined with nanoparticle encapsulation favor high effective platinum accumulation, significantly enhanced antitumor efficacy against cisplatin-resistant cancer and decreased system toxicity. it is believed that these ethacraplatin-loaded micelles have the ability of overcoming resistance of cancers toward cisplatin and will improve the prospects for chemotherapy of cisplatin-resistant cancers in the near future. (c) 2017 elsevier ltd. all rights reserved.
WOS关键词BIODEGRADABLE POLYMER ; DRUG-DELIVERY ; CANCER ; THERAPY ; PRODRUG ; NANOPARTICLES ; MITAPLATIN ; CONJUGATE ; COMPLEXES ; EFFICACY
WOS研究方向Engineering ; Materials Science
WOS类目Engineering, Biomedical ; Materials Science, Biomaterials
语种英语
WOS记录号WOS:000411420000011
出版者ELSEVIER SCI LTD
URI标识http://www.irgrid.ac.cn/handle/1471x/2177112
专题高能物理研究所
通讯作者Li, Chan; Liang, Xing-Jie
作者单位1.Chinese Acad Sci, Natl Ctr Nanosci & Technol China, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Lab Controllable Nanopharmaceut,Ctr Excellence Na, 11,First North Rd, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Beijing Municipal Inst Labour Protect, 55 Taoranting Rd, Beijing 100054, Peoples R China
4.Beijing Inst Transfus Med, Tissue Engn Lab, Beijing 1000850, Peoples R China
推荐引用方式
GB/T 7714
Li, Shuyi,Li, Chan,Jin, Shubin,et al. Overcoming resistance to cisplatin by inhibition of glutathione s-transferases (gsts) with ethacraplatin micelles in vitro and in vivo[J]. Biomaterials,2017,144:119-129.
APA Li, Shuyi.,Li, Chan.,Jin, Shubin.,Liu, Juan.,Xue, Xiangdong.,...&Liang, Xing-Jie.(2017).Overcoming resistance to cisplatin by inhibition of glutathione s-transferases (gsts) with ethacraplatin micelles in vitro and in vivo.Biomaterials,144,119-129.
MLA Li, Shuyi,et al."Overcoming resistance to cisplatin by inhibition of glutathione s-transferases (gsts) with ethacraplatin micelles in vitro and in vivo".Biomaterials 144(2017):119-129.

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来源:高能物理研究所

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