Targeted Therapy against Metastatic Melanoma Based on Self-Assembled Metal-Phenolic Nanocomplexes Comprised of Green Tea Catechin

被引:151
作者
Li, Ke [1 ,2 ]
Xiao, Gao [3 ,4 ]
Richardson, Joseph J. [5 ,6 ]
Tardy, Blaise L. [7 ]
Ejima, Hirotaka [8 ]
Huang, Wen [2 ]
Guo, Junling [1 ,3 ,9 ]
Liao, Xuepin [1 ]
Shi, Bi [1 ,9 ]
机构
[1] Sichuan Univ, Dept Biomass Chem & Engn, Chengdu 610065, Sichuan, Peoples R China
[2] Sichuan Univ, Regenerat Med Res Ctr, West China Hosp, Lab Ethnopharmacol, Chengdu 610041, Sichuan, Peoples R China
[3] Harvard Univ, Wyss Inst Biol Inspired Engn, John A Paulson Sch Engn & Appl Sci, Boston, MA 02115 USA
[4] Fuzhou Univ, Coll Environm & Resources, Dept Environm Sci & Engn, Fuzhou 350108, Fujian, Peoples R China
[5] Univ Melbourne, ARC Ctr Excellence Convergent Bionano Sci & Techn, Parkville, Vic 3010, Australia
[6] Univ Melbourne, Dept Chem & Biomol Engn, Parkville, Vic 3010, Australia
[7] Aalto Univ, Dept Bioprod & Biosyst, Sch Chem Engn, POB 16300, Aalto 00076, Finland
[8] Univ Tokyo, Dept Mat Engn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
[9] Sichuan Univ, Natl Engn Lab Clean Technol Leather Manufacture, Chengdu 610065, Sichuan, Peoples R China
基金
中国国家自然科学基金; 日本学术振兴会;
关键词
metal-phenolic network; metastatic melanoma; polyphenols; self-assembly; targeted therapy; TUMOR-METASTASIS; DELIVERY; NANOPARTICLES; LYMPHANGIOGENESIS; MICROENVIRONMENT; PLATFORM; PHASE; CELLS;
D O I
10.1002/advs.201801688
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The targeted therapy of metastatic melanoma is an important yet challenging goal that has received only limited attention to date. Herein, green tea polyphenols, (-)-epigallocatechin-3-gallate (EGCG), and lanthanide metal ions (Sm3+) are used as building blocks to engineer self-assembled Sm-III-EGCG nanocomplexes with synergistically enhanced tumor inhibitory properties. These nanocomplexes have negligible systemic toxic effects on healthy cells but cause a significant reduction in the viability of melanoma cells by efficiently regulating their metabolic pathways. Moreover, the wound-induced migration of melanoma cells can be efficiently inhibited by Sm-III -EGCG, which is a key criterion for metastatic melanoma therapy. In a mouse melanoma tumor model, Sm-III-EGCG is directly compared with a clinical anticancer drug, 5-fluorouracil and shows remarkable tumor inhibition. Moreover, the targeted therapy of Sm-III-EGCG is shown to prevent metastatic lung melanoma from spreading to main organs with no adverse side effects on the body weight or organs. These in vivo results demonstrate significant advantages of Sm-III-EGCG over its clinical counterpart. The results suggest that these green tea-based, self-assembled nanocomplexes possess all of the key traits of a clinically promising candidate to address the challenges associated with the treatment of advanced stage metastatic melanoma.
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页数:7
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