首页> 美国卫生研究院文献>other >Synthesis and Cell-Selective Antitumor Properties of Amino Acid Conjugated Tumor-Associated Carbohydrate Antigen-Coated Gold Nanoparticles
【2h】

Synthesis and Cell-Selective Antitumor Properties of Amino Acid Conjugated Tumor-Associated Carbohydrate Antigen-Coated Gold Nanoparticles

机译:氨基酸缀合的肿瘤相关碳水化合物抗原包被的金纳米粒子的合成和细胞选择性抗肿瘤特性。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The Thomsen Friedenreich antigen (TFag) disaccharide is a tumor-associated carbohydrate antigen (TACA) found primarily on carcinoma cells and rarely expressed in normal tissue. The TFag has been shown to interact with Galectin-3 (Gal-3), one in a family of β-galactoside binding proteins. Galectins have a variety of cellular functions, and Gal-3 has been shown to be the solegalectin with anti-apoptotic activity. We have previously prepared gold nanoparticles (AuNP) coated with the TFag in various presentations as potential anti-adhesive therapeutic tools or antitumor vaccine platforms. Here we describe the synthesis of TFag-glycoamino acid conjugates attached to gold nanoparticles through a combined alkane/PEG linker, where the TFag was attached to either a serine or threonine amino acid. Particles were fully characterized by a host of biophysical techniques, and along with a control particle carrying hydroxyl-terminated linker units, were evaluated in both Gal-3 positive and negative cell lines. We show that the particles bearing the saccharides selectively inhibited tumor cell growth of the Gal-3 positive cells significantly more than the Gal-3 negative cells. In addition, the threonine-attached TF particles were more potent than the serine-attached constructs. These results support the use of AuNP as antitumor therapeutic platforms, targeted against cell lines that express specific lectins that interact with TFag.
机译:Thomsen Friedenreich抗原(TFag)二糖是一种与肿瘤相关的碳水化合物抗原(TACA),主要在癌细胞上发现,很少在正常组织中表达。 TFag已显示与Galectin-3(Gal-3)相互作用,后者是一种β-半乳糖苷结合蛋白家族。半乳凝素具有多种细胞功能,并且Gal-3已被证明是具有抗凋亡活性的单半乳凝素。我们之前已经准备了各种形式的涂有TFag的金纳米颗粒(AuNP),作为潜在的抗粘连治疗工具或抗肿瘤疫苗平台。在这里,我们描述了通过组合的烷烃/ PEG接头连接到金纳米颗粒的TFag-糖基氨基酸共轭物的合成,其中TFag连接到丝氨酸或苏氨酸氨基酸。通过多种生物物理技术对颗粒进行了充分表征,并在Gal-3阳性和阴性细胞系中评估了带有羟基末端接头单元的对照颗粒。我们表明,带有糖的颗粒选择性地比Gal-3阴性细胞明显抑制Gal-3阳性细胞的肿瘤细胞生长。另外,苏氨酸连接的TF颗粒比丝氨酸连接的构建体更有效。这些结果支持使用AuNP作为抗肿瘤治疗平台,针对表达与TFag相互作用的特定凝集素的细胞系。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号