Glucocorticoid receptor-mediated delivery of nano gold-withaferin conjugates for reversal of epithelial-to-mesenchymal transition and tumor regression

被引:39
作者
Agarwalla, Pritha [1 ,2 ]
Mukherjee, Sudip [1 ,2 ]
Sreedhar, Bojja [3 ]
Banerjee, Rajkumar [1 ,2 ]
机构
[1] IICT, CSIR, Biomat Grp, Hyderabad 500007, Telangana, India
[2] Acad Sci & Innovat Res AcSIR, 2 Rafi Marg, New Delhi 110001, India
[3] IICT, CSIR, Inorgan & Phys Chem Div, Hyderabad 500007, Telangana, India
关键词
dexamethasone; EMT reversal; glucocorticoid receptor; gold nanoparticle; tumor regression; CANCER-RELATED FATIGUE; PROSTATE-CANCER; STEM-CELLS; IN-VIVO; DEXAMETHASONE; METASTASIS; EMT; NANOPARTICLES; EXPRESSION; MELANOMA;
D O I
10.2217/nnm-2016-0224
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: To explore the potential of glucocorticoid receptor-targeted nano-gold formulation as antitumor drug sensitizing agent. Materials & methods: Simultaneous conjugation of gold nanoparticle with thiol-modified dexamethasone, a synthetic glucocorticoid and anticancer drug withaferin A afforded stable gold nanoparticle-modifed dexamethasone-withaferin A nanoconjugate. Results: This metallic nanoparticle formulation showed glucocorticoid receptor-dependent cancer cell selective cytotoxicity, inhibited growth of aggressive mouse melanoma tumor, reduced mice mortality, while reversing epithelial-to-mesenchymal transition in tumor cells. Same treatment also leads to near-complete downregulation of ABCG2 drug transporter in tumor-associated cells thus attributing it to its drug sensitizing ability. Conclusion: The presently synthesized nanoconjugate holds a great promise to sensitize cancer cells to chemotherapeutics and induce epithelial-to-mesenchymal transition reversal in tumor cells preventing metastasis.
引用
收藏
页码:2529 / 2546
页数:18
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