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微小RNA-557通过负向调控淋巴样增强因子1(LEF1)的表达,在人类肺癌中发挥肿瘤抑制作用。

MiR-557 works as a tumor suppressor in human lung cancers by negatively regulating LEF1 expression.

作者信息

Qiu Jiayong, Hao Yingying, Huang Shenshen, Ma Yaqing, Li Xiaofang, Li Danyang, Mao Yimin

机构信息

1 Department of Respiratory Medicine, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, China.

2 Department of Infectious Diseases, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, China.

出版信息

Tumour Biol. 2017 Jun;39(6):1010428317709467. doi: 10.1177/1010428317709467.

Abstract

MicroRNAs play an important role in regulating post-transcriptional gene expression in the progression of various human cancers. In this study, we investigated the role of microRNA-557 in human lung cancer cells. The molecular mechanism of microRNA-557 was also clarified in the proliferation and invasion of human lung cancer cells. Our results showed microRNA-557 levels were obviously decreased in clinical lung cancer specimens and lung cancer cell lines. Cell viability of A549 and NCI-H460 cells transfected with microRNA-557 mimics was significantly decreased than those transfected with negative control mimics. MicroRNA-557 promoted cell death of A549 and NCI-H460 but did not affect the cell apoptosis of lung cancer cells. Overexpression of microRNA-557 inhibited cell invasion of A549 and NCI-H460 cells. TargetScan analysis showed that microRNA-557 might target 3' untranslated region of lymphocyte enhancement factor 1, and the western blotting results showed that transfection of microRNA-557 mimics significantly decreased the levels of lymphocyte enhancement factor 1 in A549 and H460 cells. MicroRNA-557 might work as a tumor suppressor by negatively regulating the expression of lymphocyte enhancement factor 1 in lung cancer cells.

摘要

微小RNA在多种人类癌症进展过程中的转录后基因表达调控中发挥着重要作用。在本研究中,我们调查了微小RNA - 557在人肺癌细胞中的作用。微小RNA - 557在人肺癌细胞增殖和侵袭中的分子机制也得到了阐明。我们的结果显示,临床肺癌标本和肺癌细胞系中微小RNA - 557水平明显降低。用微小RNA - 557模拟物转染的A549和NCI - H460细胞的细胞活力显著低于用阴性对照模拟物转染的细胞。微小RNA - 557促进了A549和NCI - H460细胞的死亡,但不影响肺癌细胞的凋亡。微小RNA - 557的过表达抑制了A549和NCI - H460细胞的侵袭。TargetScan分析表明,微小RNA - 557可能靶向淋巴细胞增强因子1的3'非翻译区,蛋白质印迹结果显示,转染微小RNA - 557模拟物显著降低了A549和H460细胞中淋巴细胞增强因子1的水平。微小RNA - 557可能通过负调控肺癌细胞中淋巴细胞增强因子1的表达而发挥肿瘤抑制作用。

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