Abstract

BackgroundMicroRNA-21 (miR-21) is up-regulated in tumor tissue of patients with malignant diseases, including hepatocellular carcinoma (HCC). Elevated concentrations of miR-21 have also been found in sera or plasma from patients with malignancies, rendering it an interesting candidate as serum/plasma marker for malignancies. Here we correlated serum miR-21 levels with clinical parameters in patients with different stages of chronic hepatitis C virus infection (CHC) and CHC-associated HCC.Methodology/Principal Findings62 CHC patients, 29 patients with CHC and HCC and 19 healthy controls were prospectively enrolled. RNA was extracted from the sera and miR-21 as well as miR-16 levels were analyzed by quantitative real-time PCR; miR-21 levels (normalized by miR-16) were correlated with standard liver parameters, histological grading and staging of CHC. The data show that serum levels of miR-21 were elevated in patients with CHC compared to healthy controls (P<0.001); there was no difference between serum miR-21 in patients with CHC and CHC-associated HCC. Serum miR-21 levels correlated with histological activity index (HAI) in the liver (r = −0.494, P = 0.00002), alanine aminotransferase (ALT) (r = −0.309, P = 0.007), aspartate aminotransferase (r = −0.495, P = 0.000007), bilirubin (r = −0.362, P = 0.002), international normalized ratio (r = −0.338, P = 0.034) and γ-glutamyltransferase (r = −0.244, P = 0.034). Multivariate analysis revealed that ALT and miR-21 serum levels were independently associated with HAI. At a cut-off dCT of 1.96, miR-21 discriminated between minimal and mild-severe necroinflammation (AUC = 0.758) with a sensitivity of 53.3% and a specificity of 95.2%.Conclusions/SignificanceThe serum miR-21 level is a marker for necroinflammatory activity, but does not differ between patients with HCV and HCV-induced HCC.

Highlights

  • Hepatocellular carcinoma (HCC) is one of the most common solid tumors, rated third in mortality worldwide [1]

  • The dCT (CT-miR-21 - cycle treshold (CT)-miR-16) value negatively correlates with the serum level of miR-21. dCT of miR21 was higher in sera from healthy controls (3.4, CI: 3.0–3.8) than in sera from patients with chronic hepatitis C virus infection (CHC) and elevated serum ALT activity (2.2, CI: 2.0–2.4) (P,0.001, Fig. 1A), a parameter reflecting liver damage

  • It inhibits targets related to apoptosis and to transformation such as programmed cell death 4 and phosphatase and tensin homolog [6,22]. miR-21 is elevated in sera from patients with prostate carcinoma [12], mamma carcinoma [13,22] and HBVassociated hepatocellular carcinoma (HCC) [23], raising the possibility that it may serve as serum marker for malignant diseases

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Summary

Introduction

Hepatocellular carcinoma (HCC) is one of the most common solid tumors, rated third in mortality worldwide [1]. There are no biomarkers for the early detection of HCC, and most patients with HCC are diagnosed at advanced stages, which are associated with poor prognosis and low survival rates due to a lack of curative treatment options. MiRNAs have been detected in human serum. MicroRNA-21 (miR-21) is up-regulated in tumor tissue of patients with malignant diseases, including hepatocellular carcinoma (HCC). Elevated concentrations of miR-21 have been found in sera or plasma from patients with malignancies, rendering it an interesting candidate as serum/plasma marker for malignancies. We correlated serum miR-21 levels with clinical parameters in patients with different stages of chronic hepatitis C virus infection (CHC) and CHC-associated HCC

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