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pmid:29616093

Expression of the microRNA-143/145 cluster is decreased in hepatitis B virus-associated hepatocellular carcinoma and may serve as a biomarker for tumorigenesis in patients with chronic hepatitis B.

Qi Zhao · Xiangfei Sun · Chao Liu · Tao Li · Juan Cui · Chengyong Qin

Oncology letters · 2018 doi:10.3892/ol.2018.8117

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Experiment

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Data

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Analysis

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pmid:29616093
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title
Expression of the microRNA-143/145 cluster is decreased in hepatitis B virus-associated hepatocellular carcinoma and may serve as a biomarker for tumorigenesis in patients with chronic hepatitis B.
doi
10.3892/ol.2018.8117
pmid
29616093
authors array · 6 items
[0]
Qi Zhao
[1]
Xiangfei Sun
[2]
Chao Liu
[3]
Tao Li
[4]
Juan Cui
[5]
Chengyong Qin
journal
Oncology letters
year
2018
abstract
The aims of the present study were to identify the expression profile of microRNA (miR)-143/145 in hepatitis B virus (HBV)-associated hepatocellular carcinoma (HCC), explore its association with prognosis and investigate whether the serum miR-143/145 expression levels may serve as a diagnostic indicator of HBV-associated HCC. The microRNA (miRNA) chromatin immunoprecipitation dataset was obtained from The Cancer Genome Atlas (TCGA) and the Gene Expression Omnibus databases, and analyzed using the Wilcoxon signed-rank test. It was observed that the expression of miR-143 and miR-145 was decreased 1.5-fold in HBV-associated HCC samples compared with non-tumor tissue in the TCGA and the GSE22058 datasets (P<0.01). Using the reverse transcription-quantitative polymerase chain reaction, it was further confirmed that miR-143/145 and their host gene MIR143HG were downregulated in HBV-associated HCC tissues compared with corresponding distal non-tumor tissues. The lower level of miR-143 and miR-145 expression was associated with tumor differentiation, and may thus be responsible for a poor prognosis of patients with HBV-associated HCC. The receiver-operating characteristic (ROC) curves were used to explore the potential value of miR-143 and miR-145 as biomarkers for predicting HBV-associated HCC tumorigenesis. In serum, miR-143/145 were identified to be significantly decreased in patients with HBV-associated HCC compared with negative control patients, and their associated areas under the ROC curves were calculated at 0.813 and 0.852 (P<0.05), with each having a sensitivity and a specificity close to 0.80. These results indicated that the decreased expression of the miR-143/145 cluster and their host gene MIR143HG in HBV-associated HCC tissue was associated with prognosis, and each of these miRNAs may serve as a valuable diagnostic biomarker for predicting HBV-associated HCC tumorigenesis.
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For each dataset, the Wilcoxon signed-rank test was used to identify the differentially expressed genes between tumor and non-tumor samples.
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For each dataset, the Wilcoxon signed-rank test was used to identify the differentially expressed genes between tumor and non-tumor samples.
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The miRNA expression profile of 372 patients with HCC and 50 non-tumor distal liver samples was obtained from the TCGA dataset (cancergenome.nih.gov).
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sections[4] "TCGA miRNA dataset" paragraph 2
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The miRNA expression profile of 372 patients with HCC and 50 non-tumor distal liver samples was obtained from the TCGA dataset (cancergenome.nih.gov).
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Using the Wilcoxon signed-rank test on miRNA ChIP data obtained from TCGA and GEO, miR-143 and miR-145 expression was decreased 1.5-fold in HBV-associated HCC samples compared with non-tumor tissue (P<0.01).
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non-coding RNA (lncRNA) were examined using RT-qPCR in HCC and normal tissues. As presented in F
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Complete file
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The microRNA (miRNA) chromatin immunoprecipitation dataset was obtained from The Cancer Genome Atlas (TCGA) and the Gene Expression Omnibus databases, and analyzed using the Wilcoxon signed-rank test. It was observed that the expression of miR-143 and miR-145 was decreased 1.5-fold in HBV-associated HCC samples compared with non-tumor tissue in the TCGA and the GSE22058 datasets (P<0.01). Using the reverse transcription-quantitative polymerase chain reaction, it was further confirmed that miR-143/145 and their host gene MIR143HG were downregulated in HBV-associated HCC tissues compared with corresponding distal non-tumor tissues. The lower level of miR-143 and miR-145 expression was associated with tumor differentiation, and may thus be responsible for a poor prognosis of patients with HBV-associated HCC. The receiver-operating characteristic (ROC) curves were used to explore the potential value of miR-143 and miR-145 as biomarkers for predicting HBV-associated HCC tumorigenesis. In serum, miR-143/145 were identified to be significantly decreased in patients with HBV-associated HCC compared with negative control patients, and their associated areas under the ROC curves were calculated at 0.813 and 0.852 (P<0.05), with each having a sensitivity and a specificity close to 0.80. 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