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MiR-196a的上调通过下调喉癌中的p27来促进细胞增殖。

Upregulation of MiR-196a promotes cell proliferation by downregulating p27 in laryngeal cancer.

作者信息

Jin Cheng, Zhang Yi, Li Jiping

机构信息

Department of Otorhinolaryngology, School of Medicine, Ren Ji Hospital, Shanghai Jiao Tong University, No.145 Pujian Road, Shanghai, 200127, China.

出版信息

Biol Res. 2016 Sep 27;49(1):40. doi: 10.1186/s40659-016-0100-9.

Abstract

BACKGROUND

Accumulating evidence has confirmed that miR-196a plays a critical role in tumorigenesis and tumor progression in a variety of cancers. It has been demonstrated that miR-196a is highly up-regulated in laryngeal cancer by miRNA profiling analysis. However, the functional mechanism of miR-196a in laryngeal cancer remains unclear. This study aims to explore the mechanism of miR-196a in laryngeal cancer.

METHODS

In the present study, we conducted qPCR analysis of miR-196a expression in human laryngeal cancer and showed that miR-196a was overexpressed in tumor-derived samples and laryngeal cancer cell lines compared with matched normal controls. Further functional analysis of miR-196a demonstrated that the inhibition of miR-196a could inhibit laryngeal cell-cycle progression and proliferation in vitro. Luciferase reporter assay and western blot confirmed that miR-196a directly targeted p27kip1. Moreover, in order to investigate whether miR-196a regulated cell growth in laryngeal cancer cells by targeting p27kip1, rescue studies were performed in laryngeal cancer cells.

RESULTS

Results showed that overexpression of p27kip1 rescue decreased cell proliferation caused by miR-196a inhibitors. A negative relation between miR-196a and p27kip1 expression in laryngeal cancer tissues were also noted by further analyses.

CONCLUSIONS

The present study showed that miR-196a was upregulated in laryngeal cancer and promoted cell proliferation by downregulating p27kip1 in laryngeal cancer. However, further studies are needed to verify this finding.

摘要

背景

越来越多的证据证实,miR-196a在多种癌症的肿瘤发生和肿瘤进展中起关键作用。通过miRNA谱分析已证明miR-196a在喉癌中高度上调。然而,miR-196a在喉癌中的功能机制仍不清楚。本研究旨在探讨miR-196a在喉癌中的作用机制。

方法

在本研究中,我们对人喉癌中miR-196a的表达进行了qPCR分析,结果显示与匹配的正常对照相比,miR-196a在肿瘤来源的样本和喉癌细胞系中过表达。对miR-196a的进一步功能分析表明,抑制miR-196a可在体外抑制喉细胞周期进程和增殖。荧光素酶报告基因检测和蛋白质印迹证实miR-196a直接靶向p27kip1。此外,为了研究miR-196a是否通过靶向p27kip1调节喉癌细胞的生长,我们在喉癌细胞中进行了挽救实验。

结果

结果显示,p27kip1的过表达挽救了由miR-196a抑制剂引起的细胞增殖减少。进一步分析还发现喉癌组织中miR-196a与p27kip1表达呈负相关。

结论

本研究表明,miR-196a在喉癌中上调,并通过下调喉癌中的p27kip1促进细胞增殖。然而,需要进一步研究来验证这一发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/778e/5039793/4c2a27eb3f13/40659_2016_100_Fig1_HTML.jpg

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