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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Down-regulation of MicroRNA-381 promotes cell proliferation and invasion in colon cancer through up-regulation of LRH-1
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Down-regulation of MicroRNA-381 promotes cell proliferation and invasion in colon cancer through up-regulation of LRH-1

机译:通过LRH-1的上调促进细胞增殖和侵袭结肠癌的细胞增殖和侵袭

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The expression and roles of MicroRNA-381 (miR-381) has been explored in several types of human cancers. However, its biological functions in colon cancer remain largely unknown. Quantitative real-time PCR assays were used to detect the expression of miR-381 in human colon cancer tissues and adjacent normal tissues. miR-381 antisense oligos and mimics were introduced into SW480 and HCT116 cells. Bioinformatic prediction analysis was performed to identify the potential targets of miR-381. Protein expression analysis, luciferase assays and rescue assays were used to confirm the substrate of miR-381. We found that miR-381 was significantly down-regulated in human colon cancer tissues, compared with adjacent normal tissues. Introduction of miR-381 antisense oligos into SW480 and HCT116 cells promoted cell proliferation and invasion. Besides, inhibition of miR-381 could also support tumor growth in the nude mice. Additionally, bioinformatic prediction suggested that the nuclear receptor liver receptor homologue 1 (LRH-1) is a target gene of miR-381. Thus, our data suggested that down-regulation of miR-381 plays an important role in the colon cancer progression. (C) 2015 Published by Elsevier Masson SAS.
机译:MicroRNA-381(MIR-381)的表达和作用已在几种类型的人类癌症中探讨。然而,它在结肠癌中的生物学功能仍然很大程度上是未知的。定量实时PCR测定用于检测人结肠癌组织和相邻的正常组织中miR-381的表达。将miR-381反义寡核苷酸和模拟物引入SW480和HCT116细胞中。进行生物信息化预测分析以识别miR-381的潜在目标。使用蛋白质表达分析,荧光素酶测定和救援测定来证实miR-381的基材。与相邻的正常组织相比,我们发现miR-381在人结肠癌组织中显着下调。将miR-381反义寡核苷酸引入SW480和HCT116细胞促进细胞增殖和侵袭。此外,MiR-381的抑制还可以支持裸鼠中的肿瘤生长。另外,生物信息预测表明核受体肝受体同源物1(LRH-1)是miR-381的靶基因。因此,我们的数据表明miR-381的下调在结肠癌进展中起着重要作用。 (c)2015年由Elsevier Masson SA发布。

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