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首页> 外文期刊>Neoplasma: Journal of Experimental and Clinical Oncology >Sevoflurane inhibits migration and invasion of colorectal cancer cells by regulating microRNA-34a/ADAM10 axis
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Sevoflurane inhibits migration and invasion of colorectal cancer cells by regulating microRNA-34a/ADAM10 axis

机译:七氟醚通过调节MicroRNA-34A / ADAM10轴来抑制结直肠癌细胞的迁移和侵袭

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摘要

Sevoflurane is frequently used volatile anesthetic in cancer surgery. It has been suggested that treatment with sevoflurane could suppress migration and invasion of several human cancer cells in vitro. However, the effects of sevoflurane on colorectal cancer (CRC) remain largely unclear. In this study, CRC HCT116 and SW480 cells were treated by various concentrations of sevoflurane. MTT assay and Transwell assay were applied to evaluate the cell viability, migration and invasion abilities of CRC cell lines, respectively. Real-time quantitative PCR (RT-qPCR) was used to examine the expression level of miR-34a, and western blot assay was employed to detect the protein level of ADAM10. The target interaction between miR-34a and ADAM10 was verified through bioinformatics analysis and luciferase reporter gene assay system. Aberrant inhibitory effects induced by sevoflurane on the cell viability, migration and invasion abilities of HCT116 and SW480 cells in a dose-dependent manner were observed. Upregulation of miR-34a strikingly suppressed the cell proliferation, migration and invasion abilities of the two cell lines. Sevoflurane could facilitate the miR-34a expression and its suppressive effects on CRC cells were reversed by pre-treatment with miR-34a inhibitors. ADAM10 was identified as a downstream gene of miR-34a, downregulated by miR-34a. Overexpression of ADAM10 reverted both miR-34a and sevoflurane-induced repression in the cell proliferation, migration and invasion abilities of CRC cells. Our data showed sevoflurane inhibits the migration and invasion of colorectal cancer cells by regulating microRNA-34a/ADAM10 axis.
机译:七氟醚经常使用癌症手术中的挥发性麻醉剂。已经提出,用七氟醚处理可以在体外抑制几种人癌细胞的迁移和侵袭。然而,七氟醚对结肠直肠癌(CRC)的影响仍然很大程度上不清楚。在该研究中,通过各种浓度的七氟醚处理CRC HCT116和SW480细胞。 MTT测定和Transwell测定分别用于分别评估CRC细胞系的细胞活力,迁移和侵袭能力。使用实时定量PCR(RT-QPCR)检查miR-34a的表达水平,使用Western印迹测定检测Adam10的蛋白质水平。通过生物信息学分析和荧光素酶报告基因测定系统验证miR-34a和Adam10之间的靶相互作用。观察到七氟醚诱导的异常抑制作用对HCT116和SW480细胞的细胞活力,迁移和侵袭能力以剂量依赖性方式。 MiR-34A的上调突出地抑制了两种细胞系的细胞增殖,迁移和侵袭能力。七氟烷可以促进miR-34a表达,并通过用miR-34a抑制剂预处理反转对CRc细胞的抑制作用。 ADAM10被鉴定为MIR-34A的下游基因,由MIR-34A下调。 ADAM10的过度表达在CRC细胞的细胞增殖,迁移和侵袭能力中恢复了MIR-34A和七氟醚诱导的抑制。我们的数据显示七氟醚通过调节MicroRNA-34A / ADAM10轴来抑制结肠直肠癌细胞的迁移和侵袭。

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