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Silicate fiber scaffold-based 3D perfusion cultures of the human colorectal cancer cell line HT-29 by usinga microfluidic chip

机译:基于硅酸盐纤维支架的人大肠癌细胞系HT-29的3D灌注培养

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Three-dimensional (3D) tumor models have been established for more precise drug discovery in vitro. We previously demonstrated an in vitro 3D tumor model using silicate fiber scaffold (SFs) to assess the efficacy of potential anticancer drugs. However, mechanical forces, such as shear stress, which are known to regulate cell behavior in tissues, were absent in the model. In the present study, we developed a novel microfluidic chip that is based on a computational flow simulation. The microfluidic chip was prepared with a 3D computer aided design (CAD)/printer. The human colon adenocarcinoma cell line (HT-29) on SFs formed a mature 3D structure in this perfusion culture system and showed time-dependent drug uptake. In addition, this culture system allowed for control of the intensity of shear stress to the 3D cells by changing the fluid flow. The expression of tumor development-related genes, such as ATP synthase and CXCS4, was induced by fluid flow shear forces. This technology provides a valuable tool for future drug screening and metastasis studies.
机译:已经建立了三维(3D)肿瘤模型,用于更精确的体外药物发现。我们先前证明了使用硅酸盐纤维支架(SFs)来评估潜在抗癌药物疗效的体外3D肿瘤模型。但是,模型中缺少调节组织中细胞行为的机械力(例如剪切应力)。在本研究中,我们开发了一种基于计算流模拟的新型微流控芯片。用3D计算机辅助设计(CAD)/打印机制备微流体芯片。 SFs上的人结肠腺癌细胞系(HT-29)在此灌注培养系统中形成了成熟的3D结构,并显示出时间依赖性药物吸收。另外,该培养系统允许通过改变流体流量来控制对3D细胞的剪切应力强度。流体流动剪切力诱导了与肿瘤发展相关的基因的表达,例如ATP合酶和CXCS4。该技术为将来的药物筛查和转移研究提供了宝贵的工具。

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