Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.
Proc Natl Acad Sci U S A. 2013 Apr 23;110(17):6700-5. doi: 10.1073/pnas.1214547110. Epub 2013 Apr 8.
Although biomedical applications of nanotechnology, which typically involve functionalized nanoparticles, have taken significant strides, biological characterization of unmodified nanoparticles remains underinvestigated. Herein we demonstrate that unmodified gold nanoparticles (AuNPs) inhibit the proliferation of cancer cells in a size- and concentration-dependent manner by abrogating MAPK-signaling. In addition, these AuNPs reverse epithelial-mesenchymal transition (EMT) in cancer cells by reducing secretion of a number of proteins involved in EMT, up-regulating E-Cadherin, and down-regulating Snail, N-Cadherin, and Vimentin. Inhibition of MAPK signaling and reversal of EMT upon AuNP treatment inhibits tumor growth and metastasis in two separate orthotopic models of ovarian cancer. Western blot analyses of tumor tissues reveal up-regulation of E-Cadherin and down-regulation of Snail and phospho-MAPK, confirming the reversal of EMT and inhibition of MAPK signaling upon AuNP treatment. The ability of a single self-therapeutic nanoparticle to abrogate signaling cascades of multiple growth factors is distinctive and purports possible medical applications as potential antitumor and antimetastatic agent.
尽管生物医学领域的纳米技术应用(通常涉及功能化纳米颗粒)已经取得了显著进展,但对未经修饰的纳米颗粒的生物学特性研究仍不够充分。本文中,我们证明了未经修饰的金纳米颗粒(AuNPs)通过抑制 MAPK 信号通路,以尺寸和浓度依赖的方式抑制癌细胞的增殖。此外,这些 AuNPs 通过减少参与 EMT 的多种蛋白的分泌、上调 E-Cadherin 以及下调 Snail、N-Cadherin 和 Vimentin,逆转癌细胞的上皮间质转化(EMT)。AuNP 处理抑制 MAPK 信号通路和 EMT 的逆转,可抑制两种卵巢癌原位模型中的肿瘤生长和转移。肿瘤组织的 Western blot 分析显示 E-Cadherin 上调和 Snail 及磷酸化 MAPK 下调,证实了 EMT 的逆转和 AuNP 处理抑制 MAPK 信号通路。单个自治疗纳米颗粒能够阻断多种生长因子的信号级联反应,这一特性独特,有望作为潜在的抗肿瘤和抗转移药物应用于医学领域。