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Study on Invadopodia Formation for Lung Carcinoma Invasion with a Microfluidic 3D Culture Device

机译:微流控3D培养装置对肺癌侵袭伪足形成的研究

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摘要

Invadopodia or invasive feet, which are actin-rich membrane protrusions with matrix degradation activity formed by invasive cancer cells, are a key determinant in the malignant invasive progression of tumors and represent an important target for cancer therapies. In this work, we presented a microfluidic 3D culture device with continuous supplement of fresh media via a syringe pump. The device mimicked tumor microenvironment in vivo and could be used to assay invadopodia formation and to study the mechanism of human lung cancer invasion. With this device, we investigated the effects of epidermal growth factor (EGF) and matrix metalloproteinase (MMP) inhibitor, GM6001 on invadopodia formation by human non-small cell lung cancer cell line A549 in 3D matrix model. This device was composed of three units that were capable of achieving the assays on one control group and two experimental groups' cells, which were simultaneously pretreated with EGF or GM6001 in parallel. Immunofluorescence analysis of invadopodia formation and extracellular matrix degradation was conducted using confocal imaging system. We observed that EGF promoted invadopodia formation by A549 cells in 3D matrix and that GM6001 inhibited the process. These results demonstrated that epidermal growth factor receptor (EGFR) signaling played a significant role in invadopodia formation and related ECM degradation activity. Meanwhile, it was suggested that MMP inhibitor (GM6001) might be a powerful therapeutic agent targeting invadopodia formation in tumor invasion. This work clearly demonstrated that the microfluidic-based 3D culture device provided an applicable platform for elucidating the mechanism of cancer invasion and could be used in testing other anti-invasion agents.
机译:侵袭足或侵袭性足是侵袭性癌细胞形成的具有基质降解活性的富含肌动蛋白的膜突出物,是肿瘤恶性侵袭性进展的关键决定因素,并且代表癌症治疗的重要靶标。在这项工作中,我们提出了一种通过注射器泵连续补充新鲜培养基的微流体3D培养装置。该装置可在体内模拟肿瘤微环境,可用于检测侵袭伪足的形成并研究人肺癌的侵袭机制。使用此设备,我们在3D矩阵模型中研究了表皮生长因子(EGF)和基质金属蛋白酶(MMP)抑制剂GM6001对人非小细胞肺癌细胞A549侵袭性伪足形成的影响。该设备由三个单元组成,它们能够在一个对照组和两个实验组的细胞上进行测定,并同时用EGF或GM6001并行预处理。使用共聚焦成像系统进行侵袭伪足形成和细胞外基质降解的免疫荧光分析。我们观察到EGF促进了3D基质中A549细胞的侵袭伪足形成,而GM6001抑制了这一过程。这些结果表明,表皮生长因子受体(EGFR)信号传导在小脚伪足形成和相关的ECM降解活性中起着重要作用。同时,提示MMP抑制剂(GM6001)可能是针对肿瘤侵袭中伪足形成的有效治疗剂。这项工作清楚地证明了基于微流体的3D培养设备提供了一个可用于阐明癌症侵袭机制的平台,并可用于测试其他抗入侵剂。

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