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微小RNA-32抑制SGC-7901胃癌细胞系的增殖和侵袭。

microRNA-32 inhibits the proliferation and invasion of the SGC-7901 gastric cancer cell line .

作者信息

Zhang Jianfeng, Kuai Xiaoling, Song Mengjiao, Chen Xiaoqi, Yu Zhihua, Zhang Hong, Mao Zhenbiao

机构信息

Department of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, P.R. China.

出版信息

Oncol Lett. 2014 Jan;7(1):270-274. doi: 10.3892/ol.2013.1667. Epub 2013 Nov 7.

Abstract

microRNAs (miRNAs) are a class of endogenously expressed, small non-coding RNAs, which suppress their target mRNAs at the post-transcriptional level. miRNAs play key roles in tumor metastasis. The aim of the present study was to investigate the expression of miRNA-32 (miR-32) on the biological behavior of the human gastric cancer cell line, SGC-7901. SGC-7901 cells were transfected with miR-32-mimic, miR-32-inhibitor and empty plasmid vectors using Lipofectamine™ 2000. The expression of GFP was observed by fluorescent microscopy and miR-32 gene expression was detected by quantitative polymerase chain reaction. The cell counting kit-8 assay was performed to evaluate the effect of miR-32 expression on cell proliferation . Alterations in the migration and metastatic potential of SGC-7901 cells, prior to and following miR-32 gene transfection, were assayed by cell chemotactic migration and invasion tests. The results of the current study showed that the proliferation rate of the transfected SGC-7901 cells overexpressing miR-32 is reduced and cell chemotactic migration and invasion potentials is markedly reduced following miR-32-mimic transfection (P<0.05). In addition, the results demonstrated that overexpression of miR-32 greatly inhibits the proliferation and decreases the migration and invasion capabilities of SGC-7901 cells .

摘要

微小RNA(miRNA)是一类内源性表达的小非编码RNA,其在转录后水平抑制靶mRNA。miRNA在肿瘤转移中起关键作用。本研究的目的是探讨miRNA-32(miR-32)对人胃癌细胞系SGC-7901生物学行为的影响。使用Lipofectamine™ 2000将miR-32模拟物、miR-32抑制剂和空质粒载体转染到SGC-7901细胞中。通过荧光显微镜观察绿色荧光蛋白(GFP)的表达,并通过定量聚合酶链反应检测miR-32基因表达。进行细胞计数试剂盒-8(CCK-8)检测以评估miR-32表达对细胞增殖的影响。通过细胞趋化迁移和侵袭试验检测miR-32基因转染前后SGC-7901细胞迁移和转移潜能的变化。本研究结果表明,过表达miR-32的转染SGC-7901细胞的增殖率降低,miR-32模拟物转染后细胞趋化迁移和侵袭潜能明显降低(P<0.05)。此外,结果表明miR-32的过表达极大地抑制了SGC-7901细胞的增殖,并降低了其迁移和侵袭能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/825b/3861597/73690f0d0ec4/OL-07-01-0270-g00.jpg

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