Prediction of microRNA and gene target from an integrated network in chronic obstructive pulmonary disease based on canonical correlation analysis.

BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a complex disorder with a high mortality. The pathophysiology of COPD has not been characterized till date.
OBJECTIVE: To identify COPD-related biomarkers by a bioinformatics analysis.
METHODS: Here, we conducted the canonical correlation analysis to extract the potential COPD-related miRNAs and mRNAs based on the miRNA-mRNA dual expression profiling data. After identifying miRNAs and mRNAs related to COPD, we constructed an interaction network by integrating three validated miRNA-target sources. Then we expanded the network by adding miRNA-mRNA pairs, which were identified by Spearman rank correlation test. For miRNAs involved in the network, we further performed the Gene Ontology (GO) functional enrichment analysis of their targets. To validate COPD-related mRNAs involved in the network, we performed receiver operating characteristic (ROC) curve analysis and Support Vector Machine (SVM) classification on only those mRNAs that overlapped with COPD-related mRNAs of Online Mendelian Inheritance in Man (OMIM) database.
RESULTS: The results indicate that some identified miRNAs and their targets in the constructed network might be potential biomarkers of COPD.
CONCLUSIONS: Our study helps us to predict the potential risk biomarkers of COPD, and it can certainly help in further elucidating the genetic etiology of COPD.

Introduction

Chronic obstructive pulmonary disease (COPD) is caused by excessive exposure to highly polluted air containing high concentration of metallic oxidants. It is a chronically progressive disease that causes obstruction of airflow in patients [1]. The pathophysiology of COPD has not been understood completely till date; however, cigarette smoking is considered as an important risk factor. Previous studies have reported that oxidative stress plays a pivotal role in the pathogenesis of COPD by initiating and mediating various redox-sensitive signal transduction pathways and gene expression [2]. The pathogenesis of COPD includes multiple risk factors, including environmental [3], genetic and epigenetic components and a combination of these components. Therefore, it is important to investigate COPD-related biomarkers to comprehensively elucidate the pathogenesis of COPD.

MicroRNAs (miRNAs) are small ( 22 nucleotides) non-coding RNAs that regulate gene expression by targeting complementary mRNA [4]. MicroRNAs can target many mRNAs, and many miRNAs can cooperatively target a single mRNA. Recent studies have established that miRNAs are mediators of inflammation, which is responsible for the development and progression of COPD [5]. In recent years, several research studies have been conducted to investigate the pathogenesis of COPD. In these studies, it has been found that miRNA-mRNA regulations play a pivotal role in the pathogenesis of COPD [6]. For example, Wang et al. observed the changes in the expression of miR-145-5p, miR-338-3p and miR-3620-3p were consistent with the classification of new classification of COPD [7]. In a recent study, it has been found that miR-218-5p play a protective role in suppressing the inflammation and pathogenesis of COPD in patients who are continuously exposed to cigarette smoke [8]. Fawzy et al. found that miR-196a2 rs11614913 polymorphism is associated with the bronchodilator response of COPD in Egyptian population [9]. However, very few studies have described about the combinatorial analysis of miRNA-mRNA regulations, which are based on miRNA and mRNA dual expression profiles in patients with COPD.

To address this issue, we conducted canonical correlation analysis on miRNA-mRNA dual expression profile data in this study. The results of canonical correlation analysis were used to identify the potential miRNAs and mRNAs associated with COPD. After identifying miRNAs and mRNAs, we constructed their interaction network by integrating the three validated miRNA-target sources. Then, we expanded this network by combining miRNA-mRNA pairs based on Spearman rank correlation test. For miRNAs involved in the network, we further performed the GO functional enrichment analysis of their targets. In particular, we manually searched COPD-related genes from Online Mendelian Inheritance in Man (OMIM) database. Furthermore, we extracted genes that overlapped with target genes of miRNAs involved in the network. On these extracted genes, we performed ROC curve analysis and SVM classification to explore their potential association with COPD. The results indicate that some identified miRNAs and their targets in the constructed network might be potential risk biomarkers of COPD. The results of our study can be used to predict the potential risk biomarkers of COPD, which can then be used to comprehensively elucidate the regulatory changes associated with the development and progression of COPD.

Materials and methods

Data source

In the current study, we used miRNA-mRNA dual expression profiling data (GSE38974) to implement our analysis. MicroRNAs were profiled in subjects with 19 COPD patients and 8 normal smokers using Exiqon miRNA microarrays (GPL7723). Microarray of mRNAs was obtained from Agilent Quick Amp Labeling technologies (GPL4133), which includes 9 normal smokers and 23 COPD patients. The processing of raw miRNA and mRNA microarray data was in complete agreement with the original contribution [10]. We used SAM (Significance Analysis of Microarrays) method [11] to identify statistically significant differential expression of mRNAs and miRNAs that distinguish COPD patients from the normal smokers. To eliminate false positive discoveries and to ensure the results agreed with other sample sets of COPD, we selected more rigorous criteria of 0.01 and adjusted False Discovery Rates (FDR) 0.01 as the cutoff to filter differentially expressed miRNAs and mRNAs (genes) [12]. Based on this criterion, 134 differentially expressed miRNAs and 5,067 differentially expressed mRNAs were identified and will be used for further analysis.

Sample matching based on the propensity score

Because the sample size of miRNA and mRNA expression profile datasets was different, we could not delete samples arbitrarily. Therefore, we first performed matching using the propensity score (PS) method, which was performed in the ratio of 1:1 sub-samples on two datasets. Propensity score (PS) is often defined as the conditional probability of receiving a certain treatment from the given covariates [13]. In the current PS matching, the selected covariates are as follows: age, gender, height, weight and smoking history. The logistic regression model was used for PS matching in this analysis. As a result, four samples having lower PS score of mRNA expression profiling were discarded. Then, we performed further analysis on the miRNA-mRNA dual expression profile of 19 COPD patients as they had matching propensity score analysis.

Canonical correlation analysis

In general, canonical correlation analysis was performed to identify and measure the association between two sets of variables. It can find the two bases in which the correlation matrix between the variables is diagonal and the correlations on the diagonal are maximized [14]. It is important to note that canonical correlation method loses its effect if overfull variables are included in the analysis; therefore, we did not select the whole differentially expressed miRNAs and mRNAs to perform canonical correlation analysis. Alternatively, we only selected those differentially expressed miRNAs and mRNAs involved in the miRNA-target relationships that integrate three miRNA-target sources: miRTarBase [15], miRecords [16] and TarBase [17]. In this analysis, miRNAs were considered as the first set of variables and mRNAs as the second set of variables. Consider the number of variables exceeded the number of samples; we performed the regularized canonical correlation (RCC) to seek the potential associations between miRNAs and mRNAs. Before performing RCC on two variables sets, we used the leave-one-out criterion to determine the optimal values of two regularization parameters. The CCA package of R software (http://www.r-project.org) was used to perform canonical correlation analysis.

Network construction

For the extracted miRNAs and mRNAs from the canonical correlation analysis, except kept those miRNA-target relationships obtained from three miRNA-target sources, we expanded the network based on the associations between identified miRNAs and mRNAs. We only selected those miRNA-mRNA interactions showing significant p-values 0.05 as per Spearman correlation coefficients. In this analysis, multiple testing was not performed for two reasons: i) this allowed us to retain those interactions that had high-confidence for network construction; ii) this avoided loss information. The constructed network predicts the potential miRNA-target relationships related to COPD.

GO function enrichment analysis

In the constructed network, for each miRNA, we performed the Gene Ontology (GO) function enrichment analysis for their target genes. We used clusterProfiler package of R software (http://www.r-project.org) to implement this analysis. The multiple testing corrections based on Benjamini-Hochberg method [18] were performed; those GO terms whose adjusted p-values were less than 0.05 were considered significant.

Validation of the potential COPD-related genes involved in the network

Classification performance analysis for the identified potential COPD-related genes

To find whether the genes involved in the constructed network might be potential COPD-related genes, we manually selected genes that overlapped with COPD-related genes included in Online Mendelian Inheritance in Man (OMIM) database [19]. The area under receiver operating characteristic (ROC) curve of these overlapping genes was calculated to detect COPD. We used the expression of these overlapping genes as predictor variables, and applied Support Vector Machine (SVM) [20] to distinguish COPD patients from normal smokers. In practice, cross-validation can limit problems like overfitting and derive a more accurate estimate of model prediction performance. Because enough data was not available to partition it into “training set” and “test set”, significant modeling or testing capability would have got compromised [21]. To tackle this problem, we performed 5-fold cross validation in SVM program. In this procedure, we divided all samples into five sets. For each analysis, one set was considered as testing data whereas the remaining sets were considered as training data.

Cluster analysis by combining miRNA with mRNA expression profiling to validate the identified potential COPD-related genes

To validate the potential COPD-related genes involved in the network, we performed cluster analysis by combining miRNA with mRNA expression profile of 19 patients using Similarity Network Fusion (SNF) method [22]. SNF is a multi-omics data processing method in which the similarities between patients from different data types are integrated by a cross-network diffusion process to construct the fusion patient similarity matrix. After clustering 19 COPD patients to three clusters (subtypes), we extracted top 50 most significant differentially expressed genes distinguishing each of three clusters from normal smokers respectively, and the overlapped genes of three gene sets were extracted. Figure 1 illustrates the flowchart of our work in this analysis.

Figure 1.

The flowchart of our work. Firstly, we identified the differentially expressed miRNAs and mRNAs. Secondly, by integrating three miRNA-target sources, we performed canonical correlation analysis to identify potential COPD-related miRNAs and mRNAs. Thirdly, we constructed and expanded miRNA-mRNA network. Finally, for miRNAs involved in the network, we performed GO functional enrichment analysis of their targets. We also performed the validation of potential COPD-related genes involved in the consturction network, including ROC curve analysis, SVM classification, and cluster analysis.

Results

Canonical Correlation analysis

After integrating three miRNA-target sources into differentially expressed miRNAs and mRNAs, we used 47 differentially expressed miRNAs and 85 differentially expressed mRNAs to perform canonical correlation analysis. Based on leave-one-out criterion, we found that the optimal values of two regularization parameters were 0.25 and 0.75, respectively. After performing regularized canonical correlation, we obtained the four matrixes: the correlation between miRNA and miRNA canonical variables; the correlation between mRNA and miRNA canonical variables; the correlation between miRNA and mRNA canonical variables and the correlation between mRNA and mRNA canonical variables. For these four matrixes, we selected the correlation coefficients of the original variable and the first canonical variable because the first canonical variable had the highest canonical correlation coefficient of 0.74 (see Supplementary Fig. 1). We identified 13 miRNAs and 26 mRNAs with correlation coefficients 0.3 (see Table 1). These miRNAs and mRNAs were further used for network construction.

Table 1

The miRNAs and mRNAs identified by canonical correlation analysis

miRNA and miRNA		mRNA and miRNA		miRNA and mRNA		mRNA and mRNA
canonical variables		canonical variables		canonical variables		canonical variables
miRNA	Correlation	miRNA	Correlation	miRNA	Correlation	miRNA	Correlation
	coefficient		coefficient		coefficient		coefficient
miR-378	0.7319	CDKN1A	0.6184	miR-378	0.7460	CDKN1A	0.6548
miR-151-3p	0.6677	PAX3	0.5865	miR-519d	0.6283	PAX3	0.5976
miR-519d	0.6378	HIF1A	0.5546	miR-151-3p	0.6141	PA2G4	0.5552
miR-193b	0.5306	PA2G4	0.5341	miR-423-3p	0.5741	HIF1A	0.5449
miR-208b	0.5214	CCNF	0.5167	miR-193b	0.5412	THRAP3	0.5355
miR-423-3p	0.4523	FADD	0.5019	miR-208b	0.4790	FADD	0.5225
miR-214	0.3962	FEN1	0.4808	miR-214	0.3926	RAB1B	0.4905
miR-186	0.3700	FAF1	0.4413	miR-361-5p	0.3662	FEN1	0.4833
miR-892b	0.3661	RAB1B	0.4217	miR-186	0.3488	CCNF	0.4521
miR-326	0.3428	THRAP3	0.3925	miR-422a	0.3321	VEGFA	0.4326
miR-422a	0.3392	VEGFA	0.3722	miR-892b	0.3295	FAF1	0.4125
miR-361-5p	0.3024	ACVR1B	0.3694	miR-383	0.3126	ACVR1B	0.4017
		FGFR1	0.3682	miR-326	0.3045	CDK2	0.3998
		GPD1	0.3513			TLR2	0.3977
		PKM2	0.3423			MCL1	0.3842
		CDK2	0.3370			MAPK9	0.3750
		MAPK9	0.3211			GPD1	0.3655
		MCL1	0.3162			FGFR1	0.3522
		TLR2	0.3124			NOTCH1	0.3481
		NOTCH1	0.3083			TLR4	0.3315
		PTEN	0.3047			PTEN	0.3276
		KRAS	0.3006			ATF6B	0.3246
						KRAS	0.3162
						AKT1	0.3105
						P2RX7	0.3096
						PKM2	0.3035

After identifying 13 miRNAs and 26 mRNAs by canonical correlation analysis, we expanded the network by adding miRNA-mRNA pairs identified by Spearman rank correlation test. According to the criterion of 0.05, we added 30 miRNA-mRNA pairs to the network. Figure 2 illustrates the constructed network. As shown in Fig. 2, blue circles indicate target genes involved in three miRNA-target databases; orange circles indicate the added target genes involved in significant miRNA-mRNA pairs. Among these added miRNA-mRNA pairs, regulated relationships were observed in previous studies. For example, miR-193 was found to regulate CDK2 expression because the target ING5 of miR-193 can functionally regulate CDK2 activity [23]. To regulate the oxidation reduction mechanism, miR-378 modulates oscillation amplitudes of CDKN1A by forming partnership with different circadian transcription factors [24]. From the constructed network, we found that some target genes of miRNAs were associated with COPD. For example, FAF1 was found to be up-regulated in phlegm of COPD patients [25]. According to a recent study, ACVR1B is enriched with mutations in lung cancer cases; these subjects were included in the consensus network consisting of COPD case-control subjects [26]. In this network, we found that some added target genes were associated with COPD phenotypes. In patients with severe COPD, the reduced expression of HIF1A protein was in complete agreement with the concept of lung structure maintenance programme, which is impaired on a molecular level  [27]. The expression of TLR2 was lower in sputum neutrophils, but the expression of soluble TLR2 (sTLR2) was higher in the supernatant of COPD group. This indicates that the expression of TLR2 was down-regulated at the transit from blood to sputum [28]. In this construction network, we observed CDKN1A was regulated by multiple newly identified miRNAs, such as miR-151-3p, miR-186, and miR-214. Recent studies have proved that CDKN1A, miR-151-3p, and miR-214 are COPD-related biomarkers [2, 30, 31]; however, the obtained miRNA-target relationships need to be further validated by performing experiments of molecular biology.

Figure 2.

The constructed miRNA-mRNA regulation network. In this graph, blue circles indicate target genes involved in three miRNA-target databases, and the orange circles indicate added target genes involved in significant miRNA-mRNA pairs. Black lines indicate miRNA-mRNA relationships involved in three miRNA-target databases, and red lines indicate added miRNA-mRNA relationships involved in significant miRNA-mRNA pairs.

For each miRNA, we performed the Gene Ontology (GO) function enrichment analysis of their target genes involved in the network. Only target gene sets of miR-378 and miR-208b were enriched with some significant GO terms (see Supplementary Table 1). Figure 3 illustrates significant GO terms about biological process (BP). As shown in Fig. 3, the target genes of miR-208b were enriched on cell death and metabolic process. In a previous study conducted on mice, we found that in pulmonary endothelial or epithelial cells, the direct induction of cell apoptosis was accompanied with emphysematous changes. This implies that there are defects in these clearance mechanisms, and many evidences prove that such defects are quite common in patients with COPD [32]. Furthermore, target genes of miR-208b were enriched on GO term “localization” (GO: 0051179), which is defined as any process in which a cell, a substance, or a cellular entity is transported, tethered to, or otherwise maintained in a specific location. In practice, “localization” may also be achieved via selective degradation. In a recent COPD-related study, we found that interstitial PTX3 levels were not correlated with mRNA transcripts of whole tissue. These results indicate the lack of selection of cells relevant for PTX3 production at the chosen anatomical sites. In other words, PTX3 levels reflect selective degradation or post-transcriptional regulation [33]. Other significant functions of target genes of miR-208b and miR-378 focus on the metabolic process. In practice, we reported that skeletal muscle proteins become mobilized during inflammation. In COPD patients, the increased levels of acute phase proteins are correlated with an enhanced resting metabolic rate and fat free mass (FFM) loss [34].

Figure 3.

GO function enrichment analysis of target genes of miR-208b (A) and miR-378 (B). The significant GO terms about BP were shown in different colors. The cooler colors indicate more significant GO terms (The p-values displayed in the graph were not adjusted).

Classification performance analysis for potential COPD-related genes involved in the network

To determine whether the genes involved in the constructed network were potential COPD-related genes, we manually selected genes that overlapped with COPD-related genes included in OMIM database. We found 6 genes (HIF1A, KRAS, P2RX7, PTEN, TLR2 and VEGFA) which have been approved to be associated with COPD (see Fig. 4A). Meanwhile, the area under ROC curve (AUC) of four genes (HIF1A, KRAS, PTEN, and TLR2) was greater than 0.8, which can be used as an indicator to detect COPD in patients (see Fig. 4B). By considering the expression of these four genes as prediction variables, we classified samples by SVM method. The classification accuracy rate of HIF1A, KRAS, PTEN, and TLR2 were 91%, 97%, 81%, and 81%, respectively (see Fig. 4C). In particular, we used SVM classification plot to determine classification performance of two genes (HIF1A and KRAS) that show higher classification accuracy rate than the other two genes. The two-dimensional classification diagram showed a good classification performance in which normal smokers were distinguished well from COPD patients (see Fig. 4D).

Figure 4.

The classification performance analysis for four genes that overlap with COPD-related genes recognized in OMIM database. (A) Four overlapped genes: HIF1A, KRAS, PTEN and TLR2. (B) The ROC curve analysis for four genes. (C) The classification accuracy rate of four genes based on SVM method. (D) The SVM classification plot for HIF1A and KRAS.

As shown in Fig. 5, significant regulation ( 0.05 based on Spearman correlation coefficients) was observed between these four genes and their regulated miRNAs. Meanwhile, some identified miRNA-mRNA pairs can be indirectly and partially supported by some previous and recent literatures. For example, a variant in 3’-untranslated region of KRAS compromises its interaction with let-7g, and it contributes to the development of lung cancer in patients with COPD [35]. Interestingly, in our analysis, miR-208b is correlated with let-7g (0.544, 0.016). Therefore, there may be potential association between miR-208b and KRAS. Previous bioinformatics prediction analyses were based on sequence similarity between miRNAs and mRNAs. These prediction analyses found that some miRNAs, which were associated with COPD, contribute to the regulation of functionally relevant genes in chronic inflammatory lung disease, such as KRAS, PTEN, and TLR2 [36]. Therefore, our findings may be used as references in future studies to investigate the molecular biology of COPD. In our future study, the newly identified miRNA-mRNA pairs, such as miR-208b and KRAS, must be validated by performing an experimental study that elucidates the molecular biology of COPD.

Figure 5.

Scatter dot plots of significant regulation ( 0.05 and 0.01) between miRNAs and mRNAs: (A) miR-151-3p and HIF1A; (B) miR-423-3p and TLR2; (C) miR-208b and KRAS. The r and p values indicate the Spearman correlation coefficients and their significance respectively.

Cluster analysis by combining miRNA with mRNA expression profiling to validate the identified potential COPD-related genes

To validate the potential COPD-related genes involved in the network, we performed cluster analysis by combining miRNA with mRNA expression profile of 19 COPD patients based on SNF method. The results indicate that 19 COPD patients were divided into three clusters: A heatmap (Fig. 6A) and a silhouette plot (Fig. 6B) describe these three clusters. Cluster 1, cluster 2 and cluster 3 include 4, 7 and 8 COPD patients respectively. A higher silhouette score indicates that there is greater similarity between samples of the same cluster. In this analysis, silhouette score of cluster 1 was the highest (S 0.27). However, silhouette scores of cluster 2 and cluster 3 were comparatively lower (S 0.12 and S 0.04). For each of the three clusters, we extracted the top 50 most significant differentially expressed genes that distinguish between this cluster and normal smokers, respectively. We found that PTEN, VEGFA, and KRAS were the three common genes that were shared by three top 50 differentially expressed genes sets (Fig. 6C). Furthermore, this result indicates that the network certainly contained genes that could be considered as potential COPD-related genes.

Figure 6.

(A) Heatmap of cluster analysis based on SNF method. (B) Silhouette plot of three clusters. Silhouette score indicates the consistency within clusters of data. (C) The common genes: PTEN, VEGFA and KRAS, were shared by three top 50 differentially expressed genes sets.

Discussions

Currently, many studies have established that genetic, epigenetic, and environmental factors are risk factors responsible for the incidence and progression of COPD in general population. By performing integration data analysis, the key regulators of COPD can be identified. In the past few years, many studies have shown that miRNA-mRNA dysregulation leads to the metastasis of cancers [37]. Previous studies have reported about the effects of smoke exposure on the expression of miRNA; however, these studies have provided little information about the role of miRNAs in COPD ci38. Very few studies have reported about how miRNA-mRNA dysregulation triggers COPD in patients, because very less data is available about miRNA-mRNA dual expression profile till date. In the present study, we conducted canonical correlation analysis to extract the potential COPD-related genes: the miRNA-mRNA dual expression profile data was analyzed to determine miRNA-mRNA association with COPD. The identified genes were found to be strongly associated with the susceptibility of COPD in patients, and this observation was supported by previous and recent evidences. By performing integrative data analysis of miRNA-mRNA dual expression profile, we found that miRNA-mRNA regulation played a pivotal role in the incidence and progression of COPD. Furthermore, the novel COPD-related key regulators and biomarkers could be directly identified by this analysis.

Canonical correlation analysis (CCA) does have some limitations. Because CCA is based on linear transformations, it has limited applications in biomedical sciences. Furthermore, some identified potential biomarkers may be identified as false positive predictors by CCA. Recently, non-linear canonical correlation analysis has been developed; this technique applies non-linear functions to original variables in order to extract correlated components from two sets of variables [39]. In future studies, we will consider some new methods to implement this analysis. Another important limitation of this study is as follows: we only selected the validated miRNA-target regulations in databases, and many predicted miRNA-target regulations were not come into the analysis. Our method also does not identify regulation by translation inhibition. In addition, one of the major limitations of our analysis is the fact that there are very few miRNA-mRNA dual expression profiles related to COPD. As we know, unconvincing results are obtained by analyzing small sample sizes. In this study, we used algorithms that effectively analyzed high-dimensional data from small sample sizes, such as SAM, RCC, and SNF. Thus, we ensured that reliable results could be obtained from this analysis. We hope that more miRNA-mRNA dual expression profiles related to COPD would be available in the near future. These COPD-related profiles can then be used to perform similar analysis and to validate these results. In our current study, the identified COPD-related biomarkers were not validated by biological assays. In future studies, molecular biology experiments must be conducted to validate the findings of our study.

Another limitation of this study is that the multiple testing was not performed when filtering miRNA-mRNA pairs based on spearman correlation test. In fact, multiple testing procedures play an important role in detecting the presence of correlation. False Discovery Rate (FDR) is one of the multiple testing methods. The simple FDR estimation can be computed from p-values using Benjamini-Hochberg procedure. In this way, small p-values result in small FDR estimates. In our current study, the most significant miRNA-mRNA pairs with the smallest p-values were kept in the network. However, we could not ascertain whether those extracted miRNA-mRNA pairs that were not able to pass multiple testing were significant, and they might be the false positive discoveries.

Moreover, some studies that were based on network analysis have reported the following results: they found that the expressions of genes with differential methylation regions (DMRs) were highly negatively correlated with corresponding DNA methylations levels. This indicates that DNA methylation plays an important role in the incidence and progression of diseases [40]. Indeed, the high-throughput sequencing data analysis and the global DNA methylation analysis of airway epithelia in COPD have found some genes that are hyper-methylated and down-regulated in COPD, such as VEGFA, which is regulated by miR-378, miR-361-5p and miR-383 [41]. In the current study, we did not identify methylation events because the matched COPD-related DNA methylation data are lacking. In fact, it is preferable to combine multiple data types rather than exploiting them separately; this will be an effective strategy to identify biomarkers related to COPD. In future studies, the underlying mechanism governing complex molecular regulation must be investigated by integrating multiple data types, such as DNA methylation data, somatic mutation data, and copy number data of biological networks. These studies will help researchers to have a better understanding of biological factors, which can be used for further experimental validations and discoveries of COPD biomarkers.

Supplement Table 1

GO function enrichment analysis for miRNAs targets

miRNA	Domains	GO ID	Description	p-value	Adjusted p-value
miR-378	CC	GO:0044444	Cytoplasmic part	2.3E-03	0.0259
	CC	GO:0043234	Protein complex	4.0E-03	0.0259
	CC	GO:0032991	Macromolecular complex	9.5E-03	0.0413
	BP	GO:0051246	Regulation of protein metabolic process	1.4E-04	0.004
	BP	GO:0035556	Intracellular signal transduction	2.4E-04	0.004
	BP	GO: 0031325	Positive regulation of cellular metabolic process	3.8E-04	0.004
	BP	GO: 0048522	Positive regulation of cellular process	5.1E-04	0.004
	BP	GO: 0009893	Positive regulation of metabolic process	5.2E-04	0.004
	MF	GO:0005515	Protein binding	1.1E-02	0.0317
miR-208b	BP	GO: 0012501	Programmed cell death	2.1E-05	0.0003
	BP	GO:0008219	Cell death	4.3E-05	0.0003
	BP	GO: 0016265	Death	4.4E-05	0.0003
	BP	GO: 0006796	Phosphate-containing compound metabolic process	1.0E-03	0.0053
	BP	GO: 0006793	Phosphorus metabolic process	1.1E-03	0.0053
	BP	GO: 0048522	Positive regulation of cellular process	1.7E-03	0.0068
	BP	GO: 0048518	Positive regulation of biological process	3.2E-03	0.011
	BP	GO:0060255	Regulation of Macromolecule metabolic process	5.5E-03	0.016
	BP	GO: 0051179	Localization	6.9E-03	0.017
	BP	GO: 0031323	Regulation of cellular metabolic process	7.8E-03	0.017
	BP	GO:0080090	Regulation of primary metabolic process	8.0E-03	0.017
	BP	GO:0019222	Regulation of metabolic process	1.4E-02	0.029

CC: Cellular Component; BP: Biological Process; MF: Molecular Function.