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miR-34a和miR-217水平降低是肝细胞癌侵袭性进展和不良预后的预测生物标志物。

Decreased levels of miR-34a and miR-217 act as predictor biomarkers of aggressive progression and poor prognosis in hepatocellular carcinoma.

作者信息

Tian Yu-Wei, Shen Quan, Jiang Qing-Feng, Wang Yao-Xuan, Li Ke, Xue Huan-Zhou

机构信息

Department of Hepatobiliary Surgery, Zhengzhou University People's Hospital, Zhengzhou, China.

Department of Hepatobiliary Surgery, Zhengzhou University People's Hospital, Zhengzhou, China -

出版信息

Minerva Med. 2017 Apr;108(2):108-113. doi: 10.23736/S0026-4806.16.04616-4. Epub 2016 Nov 23.

Abstract

BACKGROUND

MicroRNAs (miRNAs) play key roles in tumor development and progression. The aim of this study was to explore the expression levels of miR-34a and miR-217 in hepatocellular carcinoma (HCC) and to further investigate the clinicopathological and prognostic value of miR-34a and miR-217.

METHODS

The expression levels of miR-34a and miR-217 were evaluated using quantitative real-time PCR (qRT-PCR). Associations between these miRNAs expression and clinicopathological features were analyzed. Survival rate was determined with Kaplan-Meier and statistically analyzed with the log-rank method between groups.

RESULTS

We found that miR-34a expression was significantly downregulated in HCC tissues (P<0.05). Reduced expression of miR-34a was associated with vascular invasion, and advanced TNM stage (P<0.05). Kaplan-Meier revealed that reduced expression of miR-34a was associated with poor overall survival (log-rank test, P<0.05). We found that miR-217 was downregulated in HCC tissues. Decreased expression of miR-217 was remarkably correlated vascular invasion, and advanced TNM stage (P<0.05). Kaplan-Meier analysis and log-rank test showed that HCC patients with low expression of miR-217 was associated with shorter overall survival than patients with high expression (log-rank test, P<0.05).

CONCLUSIONS

Our data showed that downregulation of miR-34a and miR-217 was associated with HCC progression and both of them may act as tumor suppressor in HCC.

摘要

背景

微小RNA(miRNA)在肿瘤发生和发展中起关键作用。本研究旨在探讨miR-34a和miR-217在肝细胞癌(HCC)中的表达水平,并进一步研究miR-34a和miR-217的临床病理及预后价值。

方法

采用定量实时PCR(qRT-PCR)评估miR-34a和miR-217的表达水平。分析这些miRNA表达与临床病理特征之间的关联。采用Kaplan-Meier法确定生存率,并通过对数秩检验进行组间统计学分析。

结果

我们发现miR-34a在HCC组织中的表达显著下调(P<0.05)。miR-34a表达降低与血管侵犯及TNM分期进展相关(P<0.05)。Kaplan-Meier分析显示,miR-34a表达降低与总体生存率差相关(对数秩检验,P<0.05)。我们发现miR-217在HCC组织中表达下调。miR-217表达降低与血管侵犯及TNM分期进展显著相关(P<0.05)。Kaplan-Meier分析和对数秩检验表明,miR-217低表达的HCC患者比高表达患者的总体生存期更短(对数秩检验,P<0.05)。

结论

我们的数据表明,miR-34a和miR-217的下调与HCC进展相关,且它们在HCC中均可能作为肿瘤抑制因子发挥作用。

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