Computational identification of microRNAs and their targets in liver cirrhosis
- Authors:
- Published online on: October 23, 2017 https://doi.org/10.3892/ol.2017.7252
- Pages: 7691-7698
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Copyright: © Du et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Liver cirrhosis is defined as the histological development of regenerative nodules surrounded by fibrous connective tissue in response to chronic liver disease (1). Generally, liver cirrhosis is asymptomatic and unsuspected. Liver biopsy is considered as the gold standard for diagnosis of cirrhosis, followed by assessment of risk progression according to sequential histological grading of inflammation and staging of fibrosis. However, biopsy is prone to considerable sampling variability in all liver diseases (2–5). Considering the limitations of liver biopsy, developing a reliable non-invasive and convenient method for liver cirrhosis has become an urgent requirement for early diagnosis (6–8).
MicroRNAs (miRNAs/miRs) are a class of evolutionarily conserved small (18–24 nucleotides) single-stranded non-coding RNAs, which regulate target gene expression at the post-transcriptional level by the degradation of target mRNA or the suppression of mRNA translation subsequent to its specific binding to target mRNA (9,10). In addition, miRNAs are highly stable in serum and plasma, providing the possibility of evaluating circulatory miRNA as a biomarker (11,12). Dysregulated miRNA expression has been reported in nearly all types of human cancer, including hepatocellular carcinoma (HCC) (13–15). Several miRNAs were identified as potential biomarkers for liver injury (16–20). A previous study also identified frequent and extensive dysregulation of miRNA in liver adenoma and cirrhosis, and found that different liver cancer stages may affect the dysregulation of miRNA expression (21).
Expression microarray and next-generation sequencing may reveal more differentially regulated miRNAs. However, due to the heterogeneity of the disease, variations of sample sources and diversity of analysis methods, the results of these studies are inconsistent (13). In the present study, the miRNA and mRNA expression profiles for liver cirrhosis tissues from the Gene Expression Omnibus (GEO) database were integrated. In addition, differentially expressed miRNA target genes were predicted, and a miRNA-target regulatory network was constructed. Certain key miRNAs were established as biomarkers for diagnosis, prognosis and prediction of therapeutic response.
Materials and methods
Gene expression profiles
The miRNA and mRNA expression profiles for liver cirrhosis tissues were obtained from the public repository of GEO database (http://www.ncbi.nlm.nih.gov/geo) (22). The following key words were used: ‘Liver cirrhosis’ and ‘Homo sapiens’. Previous studies that compared gene expression profiling between liver cirrhosis and normal tissues or cultured cells were included in the present study. The type of study was defined as ‘expression profiling by array’ or ‘non-coding RNA profiling by array’.
Screening of differentially expressed miRNAs and mRNAs
Raw data were preprocessed via background correction and normalization. The Limma package in R (23) was used to identify the differentially expressed miRNAs and mRNAs between liver cirrhosis tissues and controls with an unpaired t-test, then a P-value was calculated. P-values from multiple studies were combined using Fisher's exact test, and the random effects model was used to combine effect size from multiple studies. The miRNAs and mRNAs with a false discovery rate of <0.01 were regarded as differently expressed miRNAs and mRNAs.
Identification of regulatory targets for differently expressed miRNA
As the miRNAs recognize their regulatory targets through base pairing, computational methods have been invaluable for identifying these targets. The target genes for human miRNAs were downloaded from miRTarBase (http://mirtarbase.mbc.nctu.edu.tw), and the transcriptional targets of the identified miRNAs in liver cirrhosis tissues were predicted. In the present study, the differentially expressed target genes whose expression was inversely correlated with that of miRNAs were subjected to subsequent study. The miRNA-target gene interaction network in liver cirrhosis tissues was then constructed, and the network was visualized using Cytoscape (http://www.cytoscape.org) (24).
Functional enrichment analysis of differentially expressed target genes
The Database for Annotation, Visualization and Integrated Discovery (25) is the most common tool to analyze the functional enrichment of genes. To gain insights into the biological functions of miRNA target genes, Gene Ontology (GO) (26) classification and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway (27) enrichment analysis were performed. P<0.05 was selected as the cutoff criterion.
Clinical specimens
The blood samples were obtained from 5 patients with liver cirrhosis and 3 healthy volunteers. Written consent was obtained from all of the study participants, and the project was approved by the committee of Ditan Hospital (Beijing, China) for the screening, inspection and data collection from the patients.
RNA preparation and reverse transcription-quantitative polymerase chain reaction (RT-qPCR)
Total RNA was extracted using the RNAiso Plus reagent (Takara Bio, Inc., Otsu, Japan) according to the manufacturer's protocol. Total RNA (1 µg) was reverse-transcribed using a cDNA Synthesis kit (Beijing Transgen Biotech Co., Ltd., Beijing, China), and the resulting cDNA was used as the template for qPCR. qPCR was performed in a BIO-RAD IQ5 Real-Time PCR system with a PCR SYBR Green Master mix reagent kit (Beijing Transgen Biotech Co., Ltd.). Following an initial denaturing for 2 min at 94°C, qPCR was performed with 45 cycles of 94°C for 20 sec and 60°C for 34 sec. All reactions were performed in triplicate. The results were analyzed using the Cq method, using Data Assist Software version 3.0 (Applied Biosystems; Thermo Fisher Scientific, Inc., Waltham, MA, USA). The human β-actin gene was used as an endogenous control. The sequences of the PCR primers used are provided in Table I. The universal primer used for miR-21, miR-199a-3p and U6 was obtained from the miRcute Plus miRNA qPCR Detection kit (SYBR-Green) (cat. no. FP411; Tiangen Biotech Co., Ltd.). Data were analyzed with a one-way analysis of variance and Tukey's test using Microsoft Excel 2010 (Microsoft Corporation, Redmond, WA, USA). P<0.05 was considered to indicate a statistically significant difference.
Results
Differentially expressed miRNAs and mRNAs in liver cirrhosis tissues
In total, 4 mRNA expression profiling studies and 2 miRNA expression profiling studies that met the inclusion criteria were included. The characteristics of each study are summarized in Table II. Of these studies, 166 cases of liver cirrhosis and 64 controls were analyzed.
Following normalization of the original miRNA and mRNA expression datasets, a total of 48 differentially expressed miRNAs were identified, including 5 that were upregulated and 43 that were downregulated (Table III). Using integrated analysis, a set of 1,773 differentially expressed genes (DEGs) were identified in liver cirrhosis tissues compared with normal tissues, including 1,037 upregulated and 736 downregulated genes.
Regulatory network of miRNAs and targets in liver cirrhosis
The miRTarBase database was used to predict the putative transcriptional targets of upregulated or downregulated miRNAs in liver cirrhosis tissues. Subsequent to comparing the putative targets with DEGs in liver cirrhosis tissues, a total of 240 miRNA-target gene pairs, whose expression was inversely correlated, were obtained. According to the miRNA-target gene pairs, a miRNA-target gene regulatory network was constructed (Fig. 1). In the network, the top three miRNAs (miR-21, miR-18a and miR-375) regulated the majority of the target genes. Leukemia inhibitory factor (LIFR) was identified as a target of miR-21, whereas cancerous inhibitor of protein phosphatase 2A (KIAA1524) and E2F transcription factor 1 (E2F1) were identified as targets of miR-181b.
Functional enrichment analysis
GO enrichment analysis of all target genes was performed to understand their biological functions. It was identified that the significantly enriched GO terms for molecular functions were protein binding, nucleotide binding and DNA binding. The significantly enriched GO terms for cellular components were nucleus, cytoplasm and cytosol, while those for biological processes were mitotic cell cycle, cell division and DNA replication (Table IV).
The results of KEGG pathway enrichment analysis indicated that the most significantly enriched pathway was the cell cycle, which may have a significant effect on liver cirrhosis (Table V).
RT-qPCR validation
To validate the associated between miRNAs and their target genes in the regulatory network, the blood samples from 5 pairs of patients with liver cirrhosis and normal controls were used. hsa-miR-21 (P=0.1678), hsa-miR-199a-3p (P=0.0001) and KIAA1524 (P=0.0028) were selected for RT-qPCR. The RT-qPCR results indicated that the expression was consistent with the integrated analysis data (Fig. 2).
Discussion
An increasing number of studies have focused on the role of miRNAs in regulating cancer progression and metastasis, including proliferation, invasion, migration, angiogenesis and apoptosis (28,29). Emerging evidence suggests that circulating miRNAs may function as stable, reliable and non-invasive diagnostic biomarkers for cancer (30). In the present study, 2 miRNA expression profiling studies and 4 mRNA expression profiling studies of liver cirrhosis tissues were integrated, and a set of 48 differentially expressed miRNA and 1,773 DEGs were identified. By bioinformatics prediction, a total of 240 miRNA-target gene pairs were obtained, whose expression was inversely correlated. The miRNA-targets regulatory network was constructed for liver cirrhosis tissues. In the miRNA-targets regulatory network, it was identified that the top ten upregulated and downregulated miRNAs were hsa-miR-212, hsa-miR-21, hsa-miR-199a-3p, hsa-miR-142-5p, hsa-miR-142-3p, hsa-miR-132, hsa-miR-139-5p, hsa-miR-181b, hsa-miR-21* and hsa-miR-18a, and the majority of them had previously been identified to be closely associated with alcoholic liver disease, hepatic fibrogenesis, liver cirrhosis or hepatocellular carcinoma (31–34).
Several miRNAs are involved in hepatic fibrogenesis (20,35,36). It was previously suggested that miR-21 was upregulated at the onset of fibrosis in the human liver, and that it may promote fibrogenic activation of fibroblasts (37,38) and be involved in the amplification of certain important cellular signaling pathways (39,40). A recent study also indicated that a significant elevation of hepatic miR-21 expression is associated with mitogen-activated protein kinase 3 signaling and epithelial-mesenchymal transition in liver fibrosis (34). The miR-199 family is associated with liver fibrosis. By comprehensive analysis, Murakami et al (41) identified that the high expression of 4 miRNAs (miR-199a, miR-199a*, miR-200a and miR-200b) were closely associated with the progression of liver fibrosis in humans and mice. Consistent with this, the present study revealed that miR-21 and miR-199a-3p were also significantly upregulated in liver cirrhosis tissues, implying that they may serve an important role in the progression of liver cirrhosis and that they may be promising biomarkers for the early diagnosis of liver cirrhosis.
A previous study demonstrated that the other two miRNAs, miR-142-3p and miR-142-5p, were significantly downregulated in HCC, and that they may cooperatively regulate cell movement (42). Conversely, the results of the present study indicated that miR-142-5p and miR-142-3p were significantly upregulated in liver cirrhosis tissues compared with normal tissues, implying that the expression pattern of these 2 miRNAs may be particular to liver cirrhosis, and that they may serve different roles in liver cirrhosis and HCC by a currently unknown mechanism.
In addition, Wang et al (43) identified that the expression of miR-181b may be induced by transforming growth factor-β1, which serves an important role in liver cirrhosis. miR-132 expression may be induced following alcohol intake, and it was previously shown to be increased in alcoholic liver disease (31). It was indicated that serum miR-18a was significantly higher in patients infected with hepatitis B virus (HBV) with HCC compared with healthy controls, and it may be used in discriminating HBV-associated HCC from chronic hepatitis or cirrhosis (32). Notably, in the present study, the aforementioned 3 miRNAs (miR-181b, miR-132 and miR-18a) were significantly downregulated in liver cirrhosis tissues compared with normal tissues, indicating that they may exhibit potential for diagnostic and therapeutic applications in liver cirrhosis.
In order to additionally investigate the role of miRNAs in liver cirrhosis, the transcriptional targets of the identified miRNAs in liver cirrhosis tissues were predicted, and several targets were noted, including LIFR, KIAA1524 and E2F1. It was observed that the LIFRβ subunit is intensely expressed in reactive bile ductductuules in the cirrhotic liver, in which bile duct proliferation occurs frequently (44). Previous studies have demonstrated that KIAA1524 is a cellular inhibitor of protein phosphatase 2A, which is an important tumor-suppressor protein, and that the inhibition of KIAA1524 may determine the apoptotic effects of erlotinib on HCC cells (45–47). An additional important target was E2F1, which is considered a novel fibrogenic gene, and was identified to be highly upregulated in human liver cirrhotic specimens (48). Additionally, experiments in mice demonstrated that E2F1-deficiency may largely inhibit the development of biliary liver fibrosis (48). In the present study, the dysregulation of LIFR, KIAA1524 and E2F1 in the cirrhotic liver clearly suggested their importance in the development of liver cirrhosis. The results of the function enrichment analysis of the target genes indicated that the cell cycle was the most significantly enriched pathway. This result is consistent with the importance of the cell cycle in various types of cancer (49).
In conclusion, a set of 48 differentially expressed miRNAs and 1,773 DEGs were identified in liver cirrhosis tissues compared with normal tissues. A total of 240 miRNA-target gene pairs whose expression was inversely correlated were identified. Additionally, a global miRNAs-target regulatory network was constructed, which was expected to improve the understanding of the regulatory mechanisms of liver cirrhosis pathology, and to provide a clearer biomarker for diagnosis and safer therapeutic strategies of liver cirrhosis. Additional functional studies are required to confirm the regulative associations between the miRNAs and their predictive targets.
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