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微小RNA-3191通过调控PAK6促进肝细胞癌的增殖和转移。

miR-3191 promotes the proliferation and metastasis of hepatocellular carcinoma via regulating PAK6.

作者信息

Xie Anqi, Wang Hengjie, Huang Jingchen, Sun Minmin, Chen Lin

机构信息

Community Health Service Center, Zhongshan Street, Songjiang District, Shanghai, China.

Department of Hepatic Surgery, Kunshan Hospital of Traditional Chinese Medicine, Kunshan, Jiangsu Province, 215300, China.

出版信息

Infect Agent Cancer. 2024 Dec 18;19(1):64. doi: 10.1186/s13027-024-00628-w.

Abstract

BACKGROUND/AIMS: microRNAs (miRNAs) contribute to tumorigenesis, progression and drug resistance of hepatocellular carcinoma (HCC). miR-3191 is a newly discovered miRNA, and its function and mechanism of action in biological processes and diseases are not completely understood.

METHODS

miR-3191 expression is determined via quantitative real-time polymerase chain reaction. Knockdown and overexpression of miR-3191 influence the proliferation and metastasis of HCC cells, which is measured by Cell Counting Kit-8 assay, Colony Formation assay and Cell metastasis assay. Protein expression is estimated by Western blot. The interplay between miR-3191 and target is validated by dual-luciferase reporter assay.

RESULTS

Here, we show that miR-3191 is upregulated in HCC tissues and associated with poor prognosis of HCC patients. Mechanistically, p21-activated protein kinase 6 (PAK6) was identified as a direct target of miR‑3191 in HCC. PAK6 knockdown partially recovered interference of miR‑3191‑induced decrease in cell proliferation and invasion. The accuracy of HCC patient prognosis could be improved by employing a combination of miR-3191 and PAK6 values.

CONCLUSIONS

miR-3191 promotes the proliferation and metastasis of HCC cells via targeting PAK6 and may serve as a prognostic biomarker and potential therapeutic target.

摘要

背景/目的:微小RNA(miRNA)有助于肝细胞癌(HCC)的肿瘤发生、进展和耐药性。miR-3191是一种新发现的miRNA,其在生物过程和疾病中的功能及作用机制尚未完全明确。

方法

通过定量实时聚合酶链反应测定miR-3191的表达。采用细胞计数试剂盒-8法、集落形成试验和细胞转移试验检测miR-3191的敲低和过表达对肝癌细胞增殖和转移的影响。通过蛋白质印迹法评估蛋白质表达。采用双荧光素酶报告基因试验验证miR-3191与靶标的相互作用。

结果

在此,我们发现miR-3191在肝癌组织中上调,且与肝癌患者的不良预后相关。机制上,p21活化蛋白激酶6(PAK6)被确定为肝癌中miR-3191的直接靶标。PAK6敲低部分恢复了miR-3191诱导的细胞增殖和侵袭减少的干扰。联合使用miR-3191和PAK6值可提高肝癌患者预后的准确性。

结论

miR-3191通过靶向PAK6促进肝癌细胞的增殖和转移,可能作为一种预后生物标志物和潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0656/11654304/43fe463c13fd/13027_2024_628_Fig1_HTML.jpg

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