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Microfluidics Enabled Bottom-Up Engineering of 3D Vascularized Tumor for Drug Discovery

机译:Microfluidics使3D血管化肿瘤的自下而上工程用于药物发现

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Development of high-fidelity three-dimensional (3D) models to recapitulate the tumor microenvironment is essential for studying tumor biology and discovering anticancer drugs. Here we report a method to engineer the 3D microenvironment of human tumors, by encapsulating cancer cells in the core of microcapsules with a hydrogel shell for miniaturized 3D culture to obtain avascular microtumors first. The microtumors are then used as the building blocks for assembling with endothelial cells and other stromal cells to create macroscale 3D vascularized tumor. Cells in the engineered 3D microenvironment can yield significantly larger tumors in vivo than 2D-cultured cancer cells. Furthermore, the 3D vascularized tumors are 4.7 and 139.5 times more resistant to doxorubicin hydrochloride (a commonly used chemotherapy drug) than avascular microtumors and 2D-cultured cancer cells, respectively. Moreover, this high drug resistance of the 3D vascularized tumors can be overcome by using nanoparticle-mediated drug delivery. The high-fidelity 3D tumor model may be valuable for studying the effect of microenvironment on tumor progression, invasion, and metastasis and for developing effective therapeutic strategy to fight against cancer.
机译:高保真三维(3D)模型重新承载肿瘤微环境对于研究肿瘤生物学和发现抗癌药物至关重要。在这里,我们通过将微胶囊的核心包封在微胶囊中与用于小型化3D培养的水凝胶壳中的癌细胞包封癌细胞来报告一种方法来提高人类肿瘤的3D微环境。然后用作与内皮细胞和其他基质细胞组装的结构块,以产生宏观血管3D血管化肿瘤。工程化3D微环境中的细胞可以在体内比2D培养的癌细胞产生显着更大的肿瘤。此外,3D血管化肿瘤分别抵抗盐酸多柔明素(常用化疗药物)的4.7%和139.5倍,分别比贫血性微观和2D培养的癌细胞。此外,通过使用纳米颗粒介导的药物递送,可以克服这种3D血管化肿瘤的这种高耐药性。高保真3D肿瘤模型对于研究微环境对肿瘤进展,侵袭和转移的影响以及发展有效的治疗策略来对抗癌症的影响。

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