Improving anticancer efficacy of (-)-epigallocatechin-3-gallate gold nanoparticles in murine B16F10 melanoma cells

被引:61
作者
Chen, Cheng-Cheung [1 ,2 ]
Hsieh, Dar-Shih [1 ,3 ]
Huang, Kao-Jean [4 ,5 ]
Chan, Yi-Lin [6 ]
Hong, Po-Da [7 ]
Yeh-, Ming-Kung [7 ,8 ,9 ]
Wu, Chang-Jer [1 ]
机构
[1] Natl Taiwan Ocean Univ, Dept Food Sci, Keelung, Taiwan
[2] Natl Def Med Ctr, Inst Prevent Med, Taipei, Taiwan
[3] Ren Ai Hosp, Dept Surg, Div Urol, New Taipei City, Taiwan
[4] Natl Dong Hwa Univ, Dept Life Sci, Hualien, Taiwan
[5] Natl Dong Hwa Univ, Inst Biotechnol, Hualien, Taiwan
[6] Natl Def Med Ctr, Grad Inst Med Sci, Taipei, Taiwan
[7] Natl Taiwan Univ Sci & Technol, Grad Inst Appl Sci & Technol, Mat Technol Program, Taipei, Taiwan
[8] Natl Def Med Ctr, Sch Pharm, Taipei, Taiwan
[9] Minist Hlth & Welf, Food & Drug Adm, Taipei, Taiwan
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2014年 / 8卷
关键词
gold nanoparticles; EGCG; anticancer; melanoma; GREEN TEA POLYPHENOLS; MALIGNANT-MELANOMA; METASTATIC MELANOMA; CANCER; SIZE; DELIVERY; EGCG; MECHANISMS; PREVENTION; APOPTOSIS;
D O I
10.2147/DDDT.S58414
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
(-)-Epigallocatechin-3-gallate (EGCG), the major bioactive constituent in green tea, has been reported to effectively inhibit the formation and development of tumors. To maximize the effectiveness of EGCG, we attached it to nanogold particles (EGCG-pNG) in various ratios to examine in vitro cytotoxicity and in vivo anti-cancer activity. EGCG-pNG showed improved anti-cancer efficacy in B16F10 murine melanoma cells; the cytotoxic effect in the melanoma cells treated with EGCG-pNG was 4.91 times higher than those treated with EGCG. The enhancement is achieved through mitochondrial pathway-mediated apoptosis as determined by annexin V assay, JC-10 staining, and caspase-3, -8, -9 activity assay. Moreover, EGCG-pNG was 1.66 times more potent than EGCG for inhibition of tumor growth in a murine melanoma model. In the hemolysis assay, the pNG surface conjugated with EGCG is most likely the key factor that contributes to the decreased release of hemoglobin from human red blood cells.
引用
收藏
页码:459 / 473
页数:15
相关论文
共 55 条
  • [1] Alisi A, 2007, NUTR REV, V65, P550, DOI 10.1111/j.1753-4887.2007.tb00280.x
  • [2] Bhatia S, 2009, ONCOLOGY-NY, V23, P488
  • [3] Chitosan reduced gold nanoparticles as novel carriers for transmucosal delivery of insulin
    Bhumkar, Devika R.
    Joshi, Hrushikesh M.
    Sastry, Murali
    Pokharkar, Varsha B.
    [J]. PHARMACEUTICAL RESEARCH, 2007, 24 (08) : 1415 - 1426
  • [4] The scope of nanoparticle therapies for future metastatic melanoma treatment
    Bombelli, Francesca Baldelli
    Webster, Carl A.
    Moncrieff, Marc
    Sherwood, Victoria
    [J]. LANCET ONCOLOGY, 2014, 15 (01) : E22 - E32
  • [5] Hepatotoxicity associated with supplements containing Chinese green tea (Camellia sinensis)
    Bonkovsky, HL
    [J]. ANNALS OF INTERNAL MEDICINE, 2006, 144 (01) : 68 - 71
  • [6] Anthracyclines induce the accumulation of mutant p53 through E2F1-dependent and -independent mechanisms
    Bug, M.
    Dobbelstein, M.
    [J]. ONCOGENE, 2011, 30 (33) : 3612 - 3624
  • [7] Gold nanoparticle-based platforms as cancer-targeted molecules delivery systems
    Chen, Cheng-Cheung
    Wu, Chang-Jer
    Yeh, Ming-Kung
    [J]. INTERNATIONAL JOURNAL OF NANOTECHNOLOGY, 2013, 10 (10-11) : 840 - 849
  • [8] The Effects of Size, Shape, and Surface Functional Group of Gold Nanostructures on Their Adsorption and Internalization by Cells
    Cho, Eun Chul
    Au, Leslie
    Zhang, Qiang
    Xia, Younan
    [J]. SMALL, 2010, 6 (04) : 517 - 522
  • [9] The golden age: gold nanoparticles for biomedicine
    Dreaden, Erik C.
    Alkilany, Alaaldin M.
    Huang, Xiaohua
    Murphy, Catherine J.
    El-Sayed, Mostafa A.
    [J]. CHEMICAL SOCIETY REVIEWS, 2012, 41 (07) : 2740 - 2779
  • [10] Toxic Effect of Silica Nanoparticles on Endothelial Cells through DNA Damage Response via Chk1-Dependent G2/M Checkpoint
    Duan, Junchao
    Yu, Yongbo
    Li, Yang
    Yu, Yang
    Li, Yanbo
    Zhou, Xianqing
    Huang, Peili
    Sun, Zhiwei
    [J]. PLOS ONE, 2013, 8 (04):