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XAV939: From a small inhibitor to a potent drug bioconjugate when delivered by gold nanoparticles

机译:XAV939:当由金纳米颗粒递送时从小型抑制剂到有效的药物生物结合物

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摘要

Nanoparticles as potential drug delivery vectors are drawing more attention every day. Here, we used gold nanopspheres (AuNSs) to selectively target the Wnt signaling pathway in human oral squamous cell carcinoma (HSC-3) cells. In a previously conducted study, XAV939, a small inhibiter, was found to strongly regulate the Wnt pathway by inhibiting the tankyrase enzyme and subsequent stabilization of cytoplasmic axin levels. In the present study, conjugating XAV939 molecules to AuNSs is found to enhance its potency by a factor of 20 over its free form in killing the HSC-3 cancer cells. Additionally, XAV 939 uptake studies have demonstrated an enhanced XAV939 bioconjugate delivery to the targeted cells compared to the passive cellular diffusion of the free drug at the same concentration. Furthermore, our study revealed that drug delivery and cytotoxicity are directly related to the size of the functionalized nanoparticles.
机译:纳米粒子作为潜在的药物传递载体每天都受到越来越多的关注。在这里,我们使用金纳米球(AuNSs)选择性靶向人口腔鳞状细胞癌(HSC-3)细胞中的Wnt信号通路。在先前进行的研究中,发现一种小抑制剂XAV939通过抑制坦古拉酶和随后稳定细胞质毒素水平来强烈调节Wnt途径。在本研究中,发现将XAV939分子与AuNSs结合后,在杀死HSC-3癌细胞时,其效能比其游离形式提高了20倍。另外,与相同浓度的游离药物的被动细胞扩散相比,XAV 939的摄取研究已证明XAV939生物缀合物向靶细胞的递送增强。此外,我们的研究表明,药物的递送和细胞毒性与功能化纳米颗粒的大小直接相关。

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