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The Analysis of Chemotherapy Resistance in Human Non-small Cell Lung Cancer Cell Line with an Integrated Microfluidic Device

机译:一种综合微流体装置的人非小细胞肺癌细胞化疗耐药性分析

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Microchip-based systems have many desirable characteristics and can be used in much cellular biological analysis. This work studied the correlation between the expression of Glucose-regulated protein-78 (GRP78) and anticancer drug VP-16 in human non-small cell lung cancer cell line SK-MES-1 using an integrated microfluidic device. A concentration gradient of stimulator (A23187) was generated in the upstream network of the device to induce the cells cultured in the downstream. Then the cells were treated by VP-16. The expression of GRP78 was detected by immunofluorescence. Apoptosis was assessed morphologically by 4'-6-Diamidino-2-phenylindol nuclear staining for the cells treated by VP-16. The expressions of GRP78 for the A23187-induced cells increased. After the treatment by VP-16, the percentage of apoptotic cells decreased with the increasing of A23187 concentration. GRP78 plays an important role in the resistance to VP-16 in SK-MES-1. This system offers a unique platform to characterize cellular responses in a high-throughput fashion.
机译:基于微芯片的系统具有许多所需的特性,可用于多种细胞生物学分析。该工作研究了使用集成微流体装置的人非小细胞肺癌细胞系SK-MES-1中葡萄糖调节蛋白-78(GRP78)和抗癌药物VP-16之间的相关性。在装置的上游网络中产生刺激器(A23187)的浓度梯度,以诱导在下游培养的细胞。然后通过VP-16处理细胞。通过免疫荧光检测GRP78的表达。通过VP-16处理的细胞的4'-6-二脒基-2-苯基吲哚核染色来评估细胞凋亡。 A23187诱导细胞GRP78的表达增加。在VP-16处理后,随着A23187浓度的增加,凋亡细胞的百分比降低。 GRP78在SK-MES-1中的抵抗力中起着重要作用。该系统提供独特的平台,以以高吞吐量方式表征蜂窝响应。

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