Literature DB >> 23108086

High expression of serum miR-17-5p associated with poor prognosis in patients with hepatocellular carcinoma.

Jianjian Zheng1, Peihong Dong, Shenmeng Gao, Ni Wang, Fujun Yu.   

Abstract

BACKGROUND: MicroRNAs (miRNAs) have been shown to play pivotal roles in diverse biological processes. Altered expressions of miR-17-5p in several tumor types have been reported. However, the expression and clinical significance of serum miR-17-5p in patients with hepatocellular carcinoma (HCC) are unclear.
METHODOLOGY: The expression of miR-17-5p was measured in the serum of paired pre-operative and post-operative groups (n=96) as well as non-relapsed and relapsed groups (n=40) by qRT-PCR. Further study was performed to analyze the correlation of miR-17-5p expression with clinicopathologic variables and the relationship between miR-17-5p expression and the prognosis of HCC patients.
RESULTS: The expression of serum miR-17-5p was significantly down-regulated in post-operative group and upregulated in relapsed group. Moreover, the expression of serum miR-17-5p was remarkably associated with the metastasis status and TNM stages (P<0.0001). Importantly, Kaplan-Meier curve analysis revealed that HCC patients with high expression of serum miR-17-5p had a significantly shortened overall survival (P=0.003). Univariate and Multivariable Cox regression analysis indicated that the expression of serum miR-17-5p was an independent risk factor for overall survival (P=0.005 and P=0.043, respectively).
CONCLUSIONS: The level of serum miR-17-5p is associated with development of HCC and can serve as a non-invasive biomarker for the prognostic prediction of HCC patients.

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Year:  2013        PMID: 23108086     DOI: 10.5754/hge12754

Source DB:  PubMed          Journal:  Hepatogastroenterology        ISSN: 0172-6390


  28 in total

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9.  Bioinformatic analysis of the membrane cofactor protein CD46 and microRNA expression in hepatocellular carcinoma.

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10.  MicroRNA-17-5p-activated Wnt/β-catenin pathway contributes to the progression of liver fibrosis.

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Journal:  Oncotarget       Date:  2016-01-05
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