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Microfluidic system for modelling 3D tumour invasion into surrounding stroma and drug screening

机译:用于造型3D肿瘤侵袭到周围基质和药物筛选的微流体系统

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摘要

Tumour invasion into the surrounding stroma is a critical step in metastasis, and it is necessary to clarify the role of microenvironmental factors in tumour invasion. We present a microfluidic system that simulated and controlled multi-factors of the tumour microenvironment for three-dimensional (3D) assessment of tumour invasion into the stroma. The simultaneous, precise and continuous arrangement of two 3D matrices was visualised to observe the migration of cancer cell populations or single cells by transfecting cells with a fluorescent protein. A vascular endothelial layer was formed to simulate transendothelial transport of nutrients, and its endothelial barrier function was verified by the diffusion of 70 kDa fluorescein isothiocyanate (FITC)-Dextran in 3D matrices. Through high-throughput cell migration tracking observation and statistic evaluation, we clarified that cell density of the tumour directly determined its invasiveness. The results suggested that increased secretion of IL-6 among both cancer cells (MDA-MB-231) and noncancerous cells (MCF-10A or HDF-n) after co-culture contributes to cancer cell invasiveness, and this was verified by an IL-6 inhibitor assay. Finally, the drug efficacy of paclitaxel was reflected as changes in cancer cell migration ability, viability, and morphology. Together, our microfluidic devices could be a useful tool to study the mechanism of tumour invasion into the stroma and to screen anti-metastatic drugs.
机译:肿瘤侵袭到周围基质是转移的关键步骤,有必要阐明微环境因素在肿瘤侵袭中的作用。我们介绍了一种微流体系统,其模拟和控制肿瘤微环境的多因素,用于三维(3D)评估肿瘤侵袭中的基质。可视化两个3D基质的同时性,精确和连续布置,以通过用荧光蛋白转染细胞来观察癌细胞群或单细胞的迁移。形成血管内皮层以模拟营养素的经过胸腔传输,其内皮阻隔功能通过70kDa荧光素异硫氰酸酯(FITC) - 在3D基质中的扩散验证。通过高吞吐细胞迁移跟踪观察和统计评价,阐明了肿瘤的细胞密度直接确定其侵袭性。结果表明,在共同培养后,癌细胞(MDA-MB-231)和非癌细胞(MCF-10A或HDF-N)增加IL-6的分泌增加,这有助于癌细胞侵袭性,并且通过IL验证了这一点-6抑制剂测定。最后,紫杉醇的药物有效性被反映为癌细胞迁移能力,生存能力和形态的变化。我们的微流体装置可以是研究肿瘤侵入到基质和筛选抗转移药物的机制的有用工具。

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