4.5 Article

Plasma minichromosome maintenance complex component 6 is a novel biomarker for hepatocellular carcinoma patients

Journal

HEPATOLOGY RESEARCH
Volume 44, Issue 13, Pages 1347-1356

Publisher

WILEY
DOI: 10.1111/hepr.12303

Keywords

circulating nucleic acids; enzyme-linked immunosorbent assay; hepatocellular carcinoma; minichromosome maintenance complex component 6; real-time quantitative polymerase chain reaction

Funding

  1. Key Bio-Medical research grant from Henan Provincial Government, Zhengzhou, China [132102310444]

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AimThis study aimed to investigate the presence of plasma minichromosome maintenance complex component 6 (MCM6) mRNA and protein levels in hepatocellular carcinoma (HCC) patients and evaluate their diagnostic value for HCC. MethodsBlood samples were collected from 61 HCC and 29 cirrhotic patients, and 30 healthy individuals. Circulating RNA was extracted from plasma of all samples. The mRNA for MCM6 were amplified and quantified by real-time polymerase chain reaction. Plasma MCM6 and -fetoprotein (AFP) protein levels were measured by enzyme-linked immunosorbent assay. ResultsIn HCC patients, MCM6 mRNA and protein levels were significantly increased over the cirrhotic and healthy controls. The levels of MCM6 mRNA and protein in the plasma of HCC patients correlated to vascular invasion (P<0.01). Higher MCM6 protein levels also correlated with tumor stage progression and lymph node metastasis. The MCM6 protein has sensitivity of 67.2% and specificity of 89.8% in differentiating total HCC from non-HCC individuals. In the AFP negative HCC group, MCM6 mRNA and protein could both detect 76.9% of HCC patients; combining the two of them increased the detection rate to 84.6%. In small HCC patients, MCM6 mRNA and protein could detect 64.3% and 71.4% of patients, respectively; combining AFP, MCM6 mRNA and MCM6 protein could detect 85.7% of small HCC patients. ConclusionOur results suggest that MCM6 mRNA and protein levels in plasma can be promising independent biomarkers for HCC, especially in AFP negative and small HCC patients.

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