Identification of potential miRNA–mRNA regulatory network contributing to pathogenesis of HBV-related HCC
Journal of Translational Medicine volume 17, Article number: 7 (2019)
Hepatitis B virus (HBV) is one of the major risk factors of hepatocellular carcinoma (HCC). Increasing evidence indicates that microRNA (miRNA)–mRNA axis is involved in HCC. However, a comprehensive miRNA–mRNA regulatory network in HBV-related HCC is still absent. This study aims to identify potential miRNA–mRNA regulatory pathways contributing to pathogenesis of HBV-related HCC.
Microarray GSE69580 was downloaded from Gene Expression Omnibus (GEO) database. GEO2R and ‘R-limma’ were used to conduct differential expression analysis. The common miRNAs appeared in the two analytic sets were screened as potential differentially expressed miRNAs (DE-miRNAs). The prognostic roles of screened DE-miRNAs in HCC were further evaluated using Kaplan–Meier plotter database. Target genes of DE-miRNAs were predicted by miRNet. Then, protein–protein interaction (PPI) networks were established for these targets via the STRING database, after which hub genes in the networks were identified by Cytoscape. Functional annotation and pathway enrichment analyses for the target genes were performed through DAVID database. Three enriched pathways related to HBV-related HCC were selected for further analysis and potential target genes commonly appeared in all three pathways were screened. Cytoscape was employed to construct miRNA-hub gene network. The expression and correlation of potential miRNAs and targets were further detected in clinical HBV-related HCC samples by qRT-PCR.
7 upregulated and 9 downregulated DE-miRNAs were accessed. 5 of 7 upregulated DE-miRNAs and 5 of 7 downregulated DE-miRNAs indicated significant prognostic roles in HCC. 2312 and 1175 target genes were predicted for the upregulated and downregulated DE-miRNAs, respectively. TP53 was identified as the hub gene in the PPI networks. Pathway enrichment analysis suggested that these predicted targets were linked to hepatitis B, pathways in cancer, microRNAs in cancer and viral carcinogenesis. Further analysis of these pathways screened 20 and 16 target genes for upregulated and downregulated DE-miRNAs, respectively. By detecting the expression of 36 target genes, six candidate target genes were identified. Finally, a potential miRNA–mRNA regulatory network was established based on the results of qRT-PCR and expression correlation analysis.
In the study, potential miRNA–mRNA regulatory pathways were identified, exploring the underlying pathogenesis and effective therapy strategy of HBV-related HCC.
As a major public health issue, hepatocellular carcinoma (HCC) is the fifth most common malignancy in men and the second leading cause of cancer-related mortality globally . HCC is also the most common primary liver cancer, approximately representing 90% of primary liver cancer cases .
Multiple risk factors are linked to the onset and progression of HCC, among which hepatitis B virus (HBV) infection is one of the leading risk factors . Reported by World Health Organization, in 2015, 257 million people were infected with HBV, and deaths caused by HBV were 0.78 million . To date, it has been well documented that the development of HBV-related HCC is a three-stage process: liver inflammation-liver cirrhosis-HCC . However, the underlying molecular mechanisms of HBV-related HCC remains largely insufficient and need to be further deeply elucidated.
MicroRNAs (miRNAs) are a group of endogenous single-strand non-coding RNA molecules that approximately contain 19–25 nucleotides . MiRNAs are found to function as key post-transcriptional regulators in a variety of cellular biological processes, such as differentiation, proliferation, apoptosis, migration and invasion . Over the past few decades, mounting studies have suggested that miRNAs can act as oncogenes or tumor suppressors in most types of cancer, including breast cancer , gastric cancer , prostate cancer  and colorectal cancer . With regard to HCC, multiple previous studies have also demonstrated that miRNAs are involved in HCC progression [11,12,13]. However, only few reports regarding the roles of miRNAs in HBV-related HCC. The team of Xiaojie Xu found that HBV X protein (HBx), a virally encoded protein exerting a crucial role in the pathogenesis of HBV-related HCC, inhibited miR-148a to fuel carcinogenesis of HCC . MiR-7/21/107 were also shown to contribute to HBx-induced HCC progression . MiR-338-3p was demonstrated to be involved in HBV preS2-induced HCC tumorigenesis by upregulation of TAZ . To our knowledge, there is no systemic and comprehensive analysis of miRNA–mRNA regulatory network in tumorigenesis of HBV-related HCC.
Combination of high-throughput technologies and bioinformatic analysis can provide researchers and scholars with unprecedent convenience in seeking novel cancer biomarkers and therapeutic targets. In this study, the miRNA expression profile from five HBV-related HCC patients was first downloaded from Gene Expression Omnibus (GEO, GSE69580). Then, we successively conducted differential expression analysis, target gene prediction, GO functional annotation, KEGG enrichment, analysis of potential target genes and construction of potential miRNA–mRNA pathways. To further validate these potential miRNA–mRNA pathways in HBV-related HCC, qRT-PCR were performed to detect the expression levels of these miRNAs and targets in HBV-related HCC clinical samples, and the correlation of miRNA and mRNA expression was finally evaluated.
Materials and methods
In the course of seeking relative datasets, we only included studies regarding comparing the miRNA expression in HBV-related HCC tissue with normal liver tissue from the Gene Expression Omnibus (GEO) database (http://www.ncbi.nlm.nih.gov/geo). Only datasets regarding clinical tissues were collected, and those datasets that studied mRNA expression in the level of cell line were excluded. The information of collected datasets containing titles and abstracts was screened. Then, those datasets of interest were further assessed. In the end, only the dataset, GSE69580 based on the platform of GPL10850 Agilent-021827 Human miRNA Microarray (V3) (miRbase release 12.0 miRNA ID version), was met the criterion and was chosen for subsequent analysis. This dataset contained five HBV-related HCC tumor tissues and five non-tumor liver tissues.
Screening of candidate DE-miRNAs
To screen differentially expressed miRNAs (DE-miRNAs) between HBV-related HCC tumor tissue and non-tumor liver tissue, two methods of differential expression analysis were successively conducted. GEO2R analytic tool provided by GEO database  was first applied to screen DE-miRNAs. Besides, another method named “R-limma” was introduced to further screen DE-miRNAs. Firstly, Series Matrix File of GSE69580 was downloaded from the GEO database. Data were then normalized using the normalizeBetweenArray function from R package ‘LIMMA’ from the Bioconductor project . Data before and after normalization were presented in Additional file 1: Figure S1. Subsequently, the differential analysis was conducted by the LIMMA package through entering related codes into R (version 3.4.4). The P value < 0.01 and |log2FC| > 2 were set as the cut-off criterion in the two methods mentioned above. The common DE-miRNAs identified by the two methods were presented as Veen diagram and identified as candidate DE-miRNAs.
Survival analysis of candidate DE-miRNAs
The Kaplan–Meier plotter (KM plotter) database, an online database established using gene expression data and survival information of cancer patients downloaded from the GEO database, was utilized to analyze the prognostic roles of screened candidate DE-miRNAs in HCC . Briefly, these miRNAs were first typed into the database. Subsequently, KM survival plots were created, and hazard ratio (HR), 95% confidence interval (CI) and log rank P-value were displayed on the webpage. Log rank P-value < 0.05 was considered as statistically significant. Only high expression of upregulated and downregulated candidate DE-miRNAs indicating an unfavorable and favorable prognosis in patients with HCC were selected for further analysis, respectively. These selected DE-miRNAs were named as potential DE-miRNAs.
Prediction and analysis of target genes of potential DE-miRNAs
The target genes of potential DE-miRNAs were predicted using miRNet (http://www.mirnet.ca/), which is an easy-to-use comprehensive tool integrated data from eleven different miRNA databases (TarBase, miRTarBase, miRecords, miRanda, miR2Disease, HMDD, PhenomiR, SM2miR, PharmacomiR, EpimiR and starBase) . Then, protein–protein interaction (PPI) network of target genes was constructed using the STRING database (http://string-db.org) . Subsequently, the hub genes in the network were identified by analyzing the degree of connectivity using Cytoscape software (version 3.6.1) .
Functional annotation and pathway enrichment analysis
The online program, the Database for Annotation, Visualization and Integrated Discovery (DAVID, http://david.abcc.ncifcrf.gov/), is a comprehensive tool for researchers and scholars to understand biological meaning behind multiple genes . In this study, DAVID was used to perform Gene Ontology (GO) functional annotation and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis for predicted target genes of potential DE-miRNAs. P-value < 0.05 was regarded as statistically significant.
Screening of genes in HBV-related HCC
This study aims to identify miRNA–mRNA regulatory pathways associated with HBV-related HCC. Therefore, after conducting KEGG pathway enrichment analysis, several HBV-related HCC pathways were selected for further analysis. For upregulated potential DE-miRNAs, three enriched pathways including hsa05161, hsa05200 and hsa05203 were screened. For downregulated potential DE-miRNAs, three enriched pathways including hsa05161, hsa05200 and hsa05206 were screened. The same genes presented in all three pathways were further chosen to study. These selected target genes were named as candidate target genes.
Construction of miRNA-hub gene network
To explore the correlation of candidate target genes with potential DE-miRNAs, Cytoscape software (version 3.6.1) was employed to construct and analyzed the miRNA-hub gene network.
Analysis of candidate target gene expression using the Oncomine and UALCAN database
Two databases, Oncomine database (http://www.oncomine.org)  and UALCAN database (http://ualcan.path.uab.edu/index.html) , were introduced to analyze the expression of these candidate target genes. Firstly, all candidate target genes were entered into the Oncomine database, which is an online cancer microarray database. P-value < 1E−4, fold change > 2 and gene rank in top 10% were set as the cut-off criterion. Only target genes of upregulated DE-miRNAs were significantly downregulated while targets genes of downregulated DE-miRNAs were significantly upregulated in HCC were identified as potential target genes. The expression levels of these potential target genes in HCC were further validated using the UALCAN database, which is a user-friendly, interactive web resource for analyzing cancer transcriptome data. P-value < 0.05 was considered as statistically significant.
The HBV-related HCC cell line, Hep3B, was obtained from the Institute of Biochemistry and Cell Biology of the Chinese Academy of Sciences (Shanghai, China). The cell line was maintained in Dulbecco’s modified Eagle’s medium (DMEM; Gibco, 12430047) containing 10% fetal bovine serum (FBS; Biological Industries, 04-0101-1, Cromwell, CT, USA), 100 mg/mL streptomycin, and 100 U/mL penicillin (Invitrogen, Shanghai, China) under a humidified atmosphere of 5% CO2 at 37 °C.
Fresh frozen HBV-related HCC clinical tissues and matched adjacent normal liver tissues were obtained from 20 patients who had undergo surgery from 2016 to 2017 at the First Affiliated Hospital of Zhejiang University School of Medicine (Hangzhou, China). Tissues were frozen and stored in liquid nitrogen. The study was approved by the Ethics Committee of the First Affiliated Hospital of Zhejiang University School of Medicine, and written informed consent from each patient was obtained.
Transfection of cell line
Hep3B cells were seeded in six-well plates, after which the miRNA mimics (50 nM) and negative control (50 nM) were transfected into the cell line by Lipofectamine™ 3000 (Invitrogen, Shanghai, China) according to the manufacturer’s instruction. The miRNA mimics and mimic NC were purchased from RiboBio Co. Ltd (Guangzhou, China).
The expression of potential DE-miRNAs and target genes in clinical samples were analyzed by qRT-PCR as previously reported . Firstly, total RNA was extracted from tissue samples using RNAiso plus Reagent (TaKaRa, Kusatsu, Japan). MiRNA reverse transcription primers and q-PCR primers were purchased from RiboBio Co. Ltd (Guangzhou, China), and mRNA q-PCR primers (Additional file 2: Table S1) were synthesized by BGI (Beijing, China). Then, total RNA was reverse-transcribed into complementary DNA (cDNA) by the PrimeScript RT Reagent Kit (TaKaRa, RR0037A). Next, q-PCR was performed in triplicates in a Roche LightCycler480 II Real-Time PCT Detection System by SYBR Premix Ex Taq (TaKaRa, RR420A). The expression level of miRNAs (relative to U6) and target genes (relative to GAPDH) were analyzed using the method of 2−ddCt.
Experiments were performed in triplicates and the results were shown as mean ± standard deviation (SD). Statistical analysis was conducted using the GraphPad Prism Software (Version 7). The differences between two groups were estimated by a two-tailed Student’s t-test. Spearman correlation coefficients were calculated to evaluate the correlations.
Candidate DE-miRNAs Identification and survival analysis
As mentioned above, two methods were employed to identify DE-miRNAs. The results of GEO2R analysis showed that there were 24 upregulated DE-miRNAs and 10 downregulated DE-miRNAs in HBV-related HCC tumor samples. There were eight upregulated DE-miRNAs and 19 downregulated DE-miRNAs in HBV-related HCC tumor samples after being compared with normal liver samples using ‘R-limma’ analytic method. Notably, as presented in Fig. 1a, b, seven upregulated DE-miRNAs and nine downregulated DE-miRNAs commonly appeared in the results of two analytic methods, so they were identified as candidate DE-miRNAs. These candidate DE-miRNAs were listed in Table 1.
To further validate these candidate DE-miRNAs, the prognostic roles of them in HCC were subsequently assessed by using KM plotter database. As shown in Fig. 1c–I, among 16 candidate DE-miRNAs, only high expression of five upregulated DE-miRNAs (miR-25-3p, miR-501-3p, miR-93-5p, miR-106b-5p and miR-21-5p) and five downregulated DE-miRNAs (miR-139-5p, let7c-5p, miR-486-5p, miR-125b-5p and miR-99a-5p) indicated a significantly unfavorable and favorable OS in patients with HCC, respectively. Therefore, these miRNAs were identified as final candidate DE-miRNAs (potential DE-miRNAs) and were selected for further analysis. None of expression of the other six candidate DE-miRNAs was significantly related to prognosis of patients with HCC.
Target prediction and analysis of candidate DE-miRNAs
The target genes of five potential upregulated and downregulated DE-miRNAs were successively predicted by miRNet. As shown in Table 2, we got total 2312 and 1175 predicted targets of the upregulated and downregulated DE-miRNAs, respectively. For the five upregulated DE-miRNAs, miR-93-5p was found to potentially target the most genes, with the number of 1220. For the five downregulated DE-miRNAs, let-7c-5p possessed the most targets, which number is 516. For better visualization, miRNA–mRNA networks were established using miRNet database as depicted in Fig. 2.
Next, PPI networks of predicted target genes of five upregulated DE-miRNAs (Fig. 3a) and five downregulated DE-miRNAs (Fig. 3b) were separately constructed using the STRING database and Cytoscape software. According to degree, the top 10 hub genes in the networks were screened out and were listed in Table 3. For upregulated DE-miRNAs, the top 10 hub genes were TP53, UBC, RPS27A, GAPDH, MYC, PHLPP2, HSP90AA1, TOP2A, MAPK1 and JUN. For downregulated DE-miRNAs, the top 10 hub genes were TP53, UBA52, MYC, AKT1, UBB, EGFR, JUN, HSP90AA1, PIK3CA and ACLY. TP53 showed the highest node degree in both two sets, which were 336 and 248, respectively.
Functional annotation and pathway enrichment analysis
GO functional annotation was first performed to understand the systematic features and biological meaning of these predicted targets using DAVID database. The GO ontology contains three categories: cellular component (CC), biological process (BP) and molecular function (MF). The top 10 GO terms of targets of upregulated DE-miRNAs were presented in Fig. 4a1–3, including nucleus and cytoplasm in the CC category, transcription DNA-templated and regulation of transcription DNA-templated in the BP category and protein binding and metal ion binding in the MF category. The top 10 GO terms of targets of downregulated DE-miRNAs were shown in Fig. 4b1–3, including nucleus and cytoplasm in the CC category, transcription DNA-templated and positive regulation of transcription from RNA polymerase II promoter in the BP category and protein binding and DNA binding in the MF category.
KEGG pathway enrichment analysis revealed that the targets of upregulated DE-miRNAs were enriched in pathways in cancer, PI3K-Akt signaling pathway, HTLV-I infection, endocytosis and microRNAs in cancer, whereas the targets of downregulated DE-miRNAs were enriched in pathways in cancer, microRNAs in cancer, PI3K-Akt signaling pathway, HTLV-I infection and proteoglycans in cancer. The top 20 enriched KEGG pathways of targets of upregulated and downregulated DE-miRNAs were presented in Fig. 5a, b, respectively.
Screening of candidate genes in HBV-related HCC
In this study, we intended to identify these miRNA–mRNA regulatory pathways involved in the onset and progression of HBV-related HCC. Thus, we selected several possibly related pathways from the results of KEGG pathway enrichment analysis for further analysis. For upregulated DE-miRNAs, three pathways including hepatitis B, pathways in cancer and viral carcinogenesis were chosen. The genes commonly appeared in all the three pathways were identified as candidate target genes for further analysis. Similarly, only the same targets of downregulated DE-miRNAs appeared in Hepatitis B, pathways in cancer and microRNAs in cancer were screened as candidate genes. Finally, as shown in Fig. 5c, d, 20 and 16 genes were selected as candidate target genes for upregulated and downregulated DE-miRNAs, respectively. For better visualization, miRNA–mRNA networks of these DE-miRNAs and relevant targets were constructed using Cytoscape software (Additional file 3: Figure S2).
It is widely acknowledged that there is an inverse relationship between miRNA expression and target gene expression . Based on this theory, the expression levels of 36 potential target genes in HCC were analyzed using two public databases. After being compared with normal samples, as presented in Additional file 4: Figure S3, only expression of JUN, PIK3R1 and STAT3 for upregulated DE-miRNAs was significantly decreased in HCC samples. For target genes of downregulated DE-miRNAs, only E2F2, E2F3 and NRAS expression was markedly upregulated. The similar results were acquired in our subsequent analysis of expression of JUN, PIK3R1, STAT3, E2F2, E2F3 and NRAS in HCC using another database, UALCAN database, and were shown in Additional file 5: Figure S4. According to these results, finally, JUN, PIK3R1, STAT3, E2F2, E2F3 and NRAS were identified as the potential target genes.
Identification of several potential miRNA–mRNA regulatory pathways in HBV-related HCC
Potential DE-miRNAs and target genes have been identified based on a series of bioinformatic analyses. By matching miRNA–mRNA pairs in miRNet database, we established a potential miRNA–mRNA regulatory network (miR-93-5p-JUN/STAT3 pathway, miR-106b-5p-STAT3 pathway, miR-21-5p-STAT3/PIK3R1 pathway, miR-125b-5p-E2F2/E2F3 pathway and miR-let7c-5p-NRAS pathway) as depicted in Fig. 6.
To validate these pathways, the expression levels of these DE-miRNAs and target genes were further detected in 20 pairs of HBV-related HCC clinical tissue samples and matched adjacent normal liver tissues. As shown in Fig. 7, in accordance with our previous analytic results, miR-93-5p, miR-106b-5p and miR-21-5p were significantly upregulated whereas miR-125b-5p and let7c-5p were markedly downregulated in HBV-related HCC compared to matched normal liver samples. Next, the expression levels of six potential targets were determined and the results were presented in Fig. 8. Among the six target genes, when compared with normal liver samples, JUN, STAT3 and PIK3R1 expression were significantly decreased in HBV-related HCC samples. Regarding to E2F2 expression, there was no significant difference between cancer tissues and normal controls. Different from the result of bioinformatics analysis, E2F3 expression were significantly downregulated in HBV-related HCC tissues. Despite no statistical significance, the expression of NRAS was markedly higher in HBV-related HCC tissues than that in matched normal liver tissues. Subsequently, we further analyzed the correlation of miRNA expression and target expression. As shown in Fig. 9, identical with our previous in silico analysis, STAT3 expression was inversely linked to the expression of miR-93-5p, miR-106b-5p and miR-21-5p. A significant negative correlation was found between PIK3R1 expression and miR-21-5p expression. Besides, we observed that NRAS expression was also conversely associated with let7c-5p expression. However, positive correlations of JUN and miR-93-5p, miR-125b-5p and E2F2 and miR-125b-5p and E2F3 were found. Transfected with the five miRNAs mimics, we found that the expression levels of these miRNAs were significantly increased (Fig. 10a). Overexpression of miR-93-5p, miR-106b-5p and miR-21-5p could distinctly attenuate STAT3 expression (Fig. 10b). When compared with negative control groups, downregulation of PIK3R1 and NRAS was also discovered in miR-21-5p and let7c-5p overexpression groups, respectively (Fig. 10b). However, no significant decrease of JUN, E2F2 and E2F3 expression were observed in Hep3B cells transfected with miR-93-5p and miR-125b-5p mimics. All these findings suggested that miR-93-5p/miR-106b-5p/miR-21-5p-STAT3, miR-21-5p-PIK3R1 and let7c-5p-NRAS may fuel the pathogenesis of HBV-related HCC.
The functional pattern of miRNA–mRNA regulatory network has been shown in the onset and progression of a variety of human diseases including cancer [28,29,30]. Moreover, a lot of studies about miRNA and mRNA expression profile in HBV-related HCC were published [19, 31,32,33,34]. However, a comprehensive miRNA–mRNA regulatory network in HBV-related HCC remains largely insufficient. In this present work, we aimed to construct the potential miRNA–mRNA regulatory network in HBV-related HCC. By the way of a series of bioinformatic analyses and experimental validation, several miRNAs, target genes and miRNA–mRNA regulatory pathways which may be involved in the development of HBV-related HCC have been identified.
Two regulatory pathways, miR-93-5p-JUN and miR-106b-5p-STAT3, are identified to contribute to the tumorigenesis of HBV-related HCC and miR-25 is also found to be upregulated in HBV-related HCC tissues than the matched normal liver tissues. MiR-106b, miR-93 and miR-25 belong to the miR-106b-25 cluster . Numerous studies have proved that miR-93-5p, miR-106b-5p and miR-25 function as oncogenic miRNAs in HCC. For example, exosomal miR-93-5p enhances proliferation and invasion of HCC via suppression of TIMP2/TP53INP1/CDKN1A ; miR-93-5p promotes HCC proliferation and epithelial–mesenchymal transition (EMT)-mediated invasion and metastasis by directly targeting PDCD4 . MiR-106b-5p activates the Wnt/β-catenin pathway by downregulating APC, thereby resulting in the enhancement of HCC proliferation ; upregulation of miR-106b-5p enhances migration and metastasis of HCC via the activation of EMT . As for miR-25, it has been reported to promote HCC growth, migration and invasion through directly targeting RhoGDI1 . Besides, miR-106b-25 cluster has already been investigated about its association with HBV-related HCC [41, 42]. All these findings support our analytic results that miR-93-5p/miR-106b-5p-STAT3 pathways may contribute to the progression of HBV-related HCC.
MiR-21-5p-PIK3R1 pathway is an oncogenic axis in HBV-related HCC in our present work. Previous studies have also shown that miR-21 can boost development of HCC [43,44,45,46]. MiR-21 can be modulated HBx, and is involved in the inhibition of apoptosis in HCC by directly targeting IL-12 . However, an opposite result was acquired in another report published by the team of Bandopadhyay . They indicated that the expression of miR-21 was negatively modulated by HBx protein. This contradiction makes certification of expression and function of miR-21 in HBV-related HCC sense. Future experimental validation of our current analytic result—the promotion of miR-21-5p-PIK3R1 pathway in carcinogenesis of HBV-related HCC—is of great significance.
Our analysis suggested that let7c-5p-NRAS and miR-125b-5p-E2F2/E2F3 are several tumor suppressive pathways in HBV-related HCC. Plenty of investigations have verified that let7c-5p hinders progression of HCC. For example, let7c-5p and miR-199a-5p cooperatively suppress migration and invasion in HCC by inhibiting MAP4K3 ; let7c-5p inhibits HCC cell proliferation and induces cell cycle arrest via the direct inhibition of CDC25A . MiR-125b-5p is also shown to function as tumor suppressor in HCC. MiR-125b-5p attenuates HCC proliferation via inhibition of Sirtuin 7 ; miR-125b-5p suppresses HCC malignancy through targeting SIRT6 . Besides, miR-125b-5p can also be served as a diagnostic biomarker of HBV-related HCC in early stage. These reports mentioned above all hint tumor suppressive roles of let7c-5p-NRAS, miR-125b-5p-E2F2 and miR-125b-5p-E2F3 in HBV-related HCC.
Subsequent experiments further supported our previous in silico analysis. Based on the present experimental results, among all identified miRNA–mRNA regulatory pathways, miR-93-5p/miR-106-5p/miR-21-5p-STAT3, miR-21-5p-PIK3R1 and let7c-5p-NRAS axes demonstrated better prospects. In the future, more emphases need to be put on these regulatory pathways.
Although we performed a comprehensive analysis and experimental validation of miRNA–mRNA regulatory network involved in HBV-related HCC and successfully identify several potential miRNA–mRNA pathways which may be possibly linked to development of HBV-related HCC, some limitations were existed in this study: (1) the sample size of the microarray used here was not large enough, only containing 10 tissue samples; (2) the multilayers of assumption including in silico identification of DE-miRNAs, search for their potential targets, analysis of the potential targets and evaluating the relationship between miRNAs and targets lacked experimental confirmation in vitro and in vivo; (3) experimental validation of potential miRNA and mRNA expression was only conducted in 20 pairs of HBV-related HCC tissues and matched normal tissues. So, future investigations with larger clinical samples and corresponding experiments are required and need to be urgently launched.
In summary, our present in silico analyses and preliminary experimental validation indicate several potential miRNA–mRNA pathways contributing to the carcinogenesis of HBV-related HCC. We hope that these findings we presented are helpful for future in-depth studies and accelerate the process of overcoming HBV-related HCC.
differentially expressed miRNA
Gene Expression Omnibus
hepatitis B virus
HBV X protein
- KM plotter:
Kyoto Encyclopedia of Genes and Genomes
Chen RG, Cheng QY, Owusu-Ansah KG, Chen J, Song GY, Xie HY, Zhou L, Xu X, Jiang DH, Zhengi SS. Cabazitaxel, a novel chemotherapeutic alternative for drug-resistant hepatocellular carcinoma. Am J Cancer Res. 2018;8:1297–306.
Montagner A, Le Cam L, Guillou H. beta-catenin oncogenic activation rewires fatty acid catabolism to fuel hepatocellular carcinoma. Gut. 2018. https://doi.org/10.1136/gutjnl-2018-316557.
An P, Xu J, Yu Y, Winkler CA. Host and viral genetic variation in HBV-related hepatocellular carcinoma. Front Genet. 2018;9:261.
Soriano V, Young B, Reau N. Report from the international conference on viral hepatitis-2017. AIDS Rev. 2018;20:58–70.
Lou W, Liu J, Gao Y, Zhong G, Ding B, Xu L, Fan W. MicroRNA regulation of liver cancer stem cells. Am J Cancer Res. 2018;8:1126–41.
Giovannetti E, Erozenci A, Smit J, Danesi R, Peters GJ. Molecular mechanisms underlying the role of microRNAs (miRNAs) in anticancer drug resistance and implications for clinical practice. Crit Rev Oncol Hematol. 2012;81:103–22.
Bai X, Han G, Liu Y, Jiang H, He Q. MiRNA-20a-5p promotes the growth of triple-negative breast cancer cells through targeting RUNX3. Biomed Pharmacother. 2018;103:1482–9.
Schmitt AM, Garcia JT, Hung T, Flynn RA, Shen Y, Qu K, Payumo AY, Peres-da-Silva A, Broz DK, Baum R, et al. An inducible long noncoding RNA amplifies DNA damage signaling. Nat Genet. 2016;48:1370–6.
Jackson BL, Grabowska A, Ratan HL. MicroRNA in prostate cancer: functional importance and potential as circulating biomarkers. BMC Cancer. 2014;14:930.
Liu N, Jiang F, Han XY, Li M, Chen WJ, Liu QC, Liao CX, Lv YF. MiRNA-155 promotes the invasion of colorectal cancer SW-480 cells through regulating the Wnt/beta-catenin. Eur Rev Med Pharmacol Sci. 2018;22:101–9.
Li Q, Li S, Wu Y, Gao F. miRNA-708 functions as a tumour suppressor in hepatocellular carcinoma by targeting SMAD3. Oncol Lett. 2017;14:2552–8.
Pan XP, Wang HX, Tong DM, Li Y, Huang LH, Wang C. miRNA-370 acts as a tumor suppressor via the downregulation of PIM1 in hepatocellular carcinoma. Eur Rev Med Pharmacol Sci. 2017;21:1254–63.
Yu Q, Yang X, Duan W, Li C, Luo Y, Lu S. miRNA-346 promotes proliferation, migration and invasion in liver cancer. Oncol Lett. 2017;14:3255–60.
Xu X, Fan Z, Kang L, Han J, Jiang C, Zheng X, Zhu Z, Jiao H, Lin J, Jiang K, et al. Hepatitis B virus X protein represses miRNA-148a to enhance tumorigenesis. J Clin Invest. 2013;123:630–45.
Chen WS, Yen CJ, Chen YJ, Chen JY, Wang LY, Chiu SJ, Shih WL, Ho CY, Wei TT, Pan HL, et al. miRNA-7/21/107 contribute to HBx-induced hepatocellular carcinoma progression through suppression of maspin. Oncotarget. 2015;6:25962–74.
Liu P, Zhang H, Liang X, Ma H, Luan F, Wang B, Bai F, Gao L, Ma C. HBV preS2 promotes the expression of TAZ via miRNA-338-3p to enhance the tumorigenesis of hepatocellular carcinoma. Oncotarget. 2015;6:29048–59.
Barrett T, Wilhite SE, Ledoux P, Evangelista C, Kim IF, Tomashevsky M, Marshall KA, Phillippy KH, Sherman PM, Holko M, et al. NCBI GEO: archive for functional genomics data sets—update. Nucleic Acids Res. 2013;41:D991–5.
Smyth GK, Michaud J, Scott HS. Use of within-array replicate spots for assessing differential expression in microarray experiments. Bioinformatics. 2005;21:2067–75.
Nagy A, Lanczky A, Menyhart O, Gyorffy B. Validation of miRNA prognostic power in hepatocellular carcinoma using expression data of independent datasets. Sci Rep. 2018;8:9227.
Fan Y, Siklenka K, Arora SK, Ribeiro P, Kimmins S, Xia J. miRNet-dissecting miRNA-target interactions and functional associations through network-based visual analysis. Nucleic Acids Res. 2016;44:W135–41.
Szklarczyk D, Franceschini A, Wyder S, Forslund K, Heller D, Huerta-Cepas J, Simonovic M, Roth A, Santos A, Tsafou KP, et al. STRING v10: protein–protein interaction networks, integrated over the tree of life. Nucleic Acids Res. 2015;43:D447–52.
Shannon P, Markiel A, Ozier O, Baliga NS, Wang JT, Ramage D, Amin N, Schwikowski B, Ideker T. Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res. 2003;13:2498–504.
da Huang W, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2009;4:44–57.
Rhodes DR, Yu J, Shanker K, Deshpande N, Varambally R, Ghosh D, Barrette T, Pandey A, Chinnaiyan AM. ONCOMINE: a cancer microarray database and integrated data-mining platform. Neoplasia. 2004;6:1–6.
Chandrashekar DS, Bashel B, Balasubramanya SAH, Creighton CJ, Ponce-Rodriguez I, Chakravarthi B, Varambally S. UALCAN: a portal for facilitating tumor subgroup gene expression and survival analyses. Neoplasia. 2017;19:649–58.
Chen D, Si W, Shen J, Du C, Lou W, Bao C, Zheng H, Pan J, Zhong G, Xu L, et al. miR-27b-3p inhibits proliferation and potentially reverses multi-chemoresistance by targeting CBLB/GRB2 in breast cancer cells. Cell Death Dis. 2018;9:188.
Giray BG, Emekdas G, Tezcan S, Ulger M, Serin MS, Sezgin O, Altintas E, Tiftik EN. Profiles of serum microRNAs; miR-125b-5p and miR223-3p serve as novel biomarkers for HBV-positive hepatocellular carcinoma. Mol Biol Rep. 2014;41:4513–9.
Cheng J, Zhuo H, Xu M, Wang L, Xu H, Peng J, Hou J, Lin L, Cai J. Regulatory network of circRNA–miRNA–mRNA contributes to the histological classification and disease progression in gastric cancer. J Transl Med. 2018;16:216.
Xue J, Zhou D, Poulsen O, Hartley I, Imamura T, Xie EX, Haddad GG. Exploring miRNA–mRNA regulatory network in cardiac pathology in Na(+)/H(+) exchanger isoform 1 transgenic mice. Physiol Genom. 2018. https://doi.org/10.1152/physiolgenomics.00048.2018.
Yang J, Song H, Cao K, Song J, Zhou J. Comprehensive analysis of Helicobacter pylori infection-associated diseases based on miRNA–mRNA interaction network. Brief Bioinform. 2018. https://doi.org/10.1093/bib/bby018.
Chen RC, Wang J, Kuang XY, Peng F, Fu YM, Huang Y, Li N, Fan XG. Integrated analysis of microRNA and mRNA expression profiles in HBx-expressing hepatic cells. World J Gastroenterol. 2017;23:1787–95.
Diaz G, Zamboni F, Tice A, Farci P. Integrated ordination of miRNA and mRNA expression profiles. BMC Genom. 2015;16:767.
Singh AK, Rooge SB, Varshney A, Vasudevan M, Bhardwaj A, Venugopal SK, Trehanpati N, Kumar M, Geffers R, Kumar V, Sarin SK. Global microRNA expression profiling in the liver biopsies of hepatitis B virus-infected patients suggests specific microRNA signatures for viral persistence and hepatocellular injury. Hepatology. 2018;67:1695–709.
Wang G, Dong F, Xu Z, Sharma S, Hu X, Chen D, Zhang L, Zhang J, Dong Q. MicroRNA profile in HBV-induced infection and hepatocellular carcinoma. BMC Cancer. 2017;17:805.
Li Y, Tan W, Neo TW, Aung MO, Wasser S, Lim SG, Tan TM. Role of the miR-106b-25 microRNA cluster in hepatocellular carcinoma. Cancer Sci. 2009;100:1234–42.
Xue X, Wang X, Zhao Y, Hu R, Qin L. Exosomal miR-93 promotes proliferation and invasion in hepatocellular carcinoma by directly inhibiting TIMP2/TP53INP1/CDKN1A. Biochem Biophys Res Commun. 2018;502:515–21.
Huang H, Wang X, Wang C, Zhuo L, Luo S, Han S. The miR-93 promotes proliferation by directly targeting PDCD4 in hepatocellular carcinoma. Neoplasma. 2017;64:770–7.
Shen G, Jia H, Tai Q, Li Y, Chen D. miR-106b downregulates adenomatous polyposis coli and promotes cell proliferation in human hepatocellular carcinoma. Carcinogenesis. 2013;34:211–9.
Yau WL, Lam CS, Ng L, Chow AK, Chan ST, Chan JY, Wo JY, Ng KT, Man K, Poon RT, Pang RW. Over-expression of miR-106b promotes cell migration and metastasis in hepatocellular carcinoma by activating epithelial-mesenchymal transition process. PLoS ONE. 2013;8:e57882.
Wang C, Wang X, Su Z, Fei H, Liu X, Pan Q. MiR-25 promotes hepatocellular carcinoma cell growth, migration and invasion by inhibiting RhoGDI1. Oncotarget. 2015;6:36231–44.
Liu Y, Zhang Y, Wen J, Liu L, Zhai X, Liu J, Pan S, Chen J, Shen H, Hu Z. A genetic variant in the promoter region of miR-106b-25 cluster and risk of HBV infection and hepatocellular carcinoma. PLoS ONE. 2012;7:e32230.
Qi F, Huang M, Pan Y, Liu Y, Liu J, Wen J, Xie K, Shen H, Ma H, Miao Y, Hu Z. A genetic variant in the promoter region of miR-106b-25 cluster predict clinical outcome of HBV-related hepatocellular carcinoma in Chinese. PLoS ONE. 2014;9:e85394.
He C, Dong X, Zhai B, Jiang X, Dong D, Li B, Jiang H, Xu S, Sun X. MiR-21 mediates sorafenib resistance of hepatocellular carcinoma cells by inhibiting autophagy via the PTEN/Akt pathway. Oncotarget. 2015;6:28867–81.
Najafi Z, Sharifi MA, Javadi G. Degradation of miR-21 induces apoptosis and inhibits cell proliferation in human hepatocellular carcinoma. Cancer Gene Ther. 2015;22:530.
Wagenaar TR, Zabludoff S, Ahn SM, Allerson C, Arlt H, Baffa R, Cao H, Davis S, Garcia-Echeverria C, Gaur R, et al. Anti-miR-21 suppresses hepatocellular carcinoma growth via broad transcriptional network deregulation. Mol Cancer Res. 2015;13:1009–21.
Wang Z, Yang H, Ren L. MiR-21 promoted proliferation and migration in hepatocellular carcinoma through negative regulation of Navigator-3. Biochem Biophys Res Commun. 2015;464:1228–34.
Yin D, Wang Y, Sai W, Zhang L, Miao Y, Cao L, Zhai X, Feng X, Yang L. HBx-induced miR-21 suppresses cell apoptosis in hepatocellular carcinoma by targeting interleukin-12. Oncol Rep. 2016;36:2305–12.
Bandopadhyay M, Banerjee A, Sarkar N, Panigrahi R, Datta S, Pal A, Singh SP, Biswas A, Chakrabarti S, Chakravarty R. Tumor suppressor micro RNA miR-145 and onco micro RNAs miR-21 and miR-222 expressions are differentially modulated by hepatitis B virus X protein in malignant hepatocytes. BMC Cancer. 2014;14:721.
Liu L, Lu L, Zheng A, Xie J, Xue Q, Wang F, Wang X, Zhou H, Tong X, Li Y, et al. MiR-199a-5p and let-7c cooperatively inhibit migration and invasion by targeting MAP4K3 in hepatocellular carcinoma. Oncotarget. 2017;8:13666–77.
Zhu X, Wu L, Yao J, Jiang H, Wang Q, Yang Z, Wu F. MicroRNA let-7c inhibits cell proliferation and induces cell cycle arrest by targeting CDC25A in human hepatocellular carcinoma. PLoS ONE. 2015;10:e0124266.
Zhao L, Wang W. miR-125b suppresses the proliferation of hepatocellular carcinoma cells by targeting Sirtuin7. Int J Clin Exp Med. 2015;8:18469–75.
Song S, Yang Y, Liu M, Liu B, Yang X, Yu M, Qi H, Ren M, Wang Z, Zou J, et al. MiR-125b attenuates human hepatocellular carcinoma malignancy through targeting SIRT6. Am J Cancer Res. 2018;8:993–1007.
WYL, SSZ and WMF designed the study. WYL and JXL wrote and revised the manuscript and performed the experiments and statistical analysis of the data. BSD, DNC, LX and JD conducted some experiments. DHJ and LZ collected clinical samples. All authors read and approved the final manuscript.
This work was supported by the National Natural Science Foundation of China (81372462, 81572987), the Department of Science and Technology of Zhejiang Province (2014C03012) and the Health and Family Planning Commission of Zhejiang Province (2012KYB045).
The authors declare that they have no competing interests.
Availability of data and materials
The microarray data were deposited in the Gene Expression Omnibus (GEO) database (Accession number: GSE69580). Besides, please contact author for data and materials requests.
Consent for publication
Ethics approval and consent to participate
This study was approved by the Ethical Committee of First Affiliated Hospital of Zhejiang University School of Medicine. In addition, relevant informed consent was acquired from each patient before surgery.
National Natural Science Foundation of China (Nos. 81372462 and 81572987) and the Department of Science and Technology of Zhejiang Province (2014C03012).
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Normalization of GSE69580. (A) Data before normalization; (B) data after normalization.
Primers sequence list.
The miRNA-hub gene networks. (A) For upregulated DE-miRNAs; (B) for downregulated DE-miRNAs.
The expression levels of screened potential target genes from the Oncomine database.
The expression levels of six screened target genes from the UALCAN database.
About this article
Cite this article
Lou, W., Liu, J., Ding, B. et al. Identification of potential miRNA–mRNA regulatory network contributing to pathogenesis of HBV-related HCC. J Transl Med 17, 7 (2019). https://doi.org/10.1186/s12967-018-1761-7