DEGs network using the information available on MirTarbase [92],
a database for experimentally validated miRNA target genes,
miRanda [93] and TargetScan [94], two databases for predicted
miRNA target genes. For each of the DETF-DEG pairs, we calcu-
lated the Pearson correlation coefficient (PCC) of expression values
and selected the significant pairs with an absolute PCC value more
than 0.4 (as TF can either trans-activate or trans-suppress their
target genes). The main regulatory effect of miRNAs is induced
through binding and degradation of their target mRNA. There-
fore, we considered only negative correlation between miRNA and
the target mRNA expression [95–97] and set the PCC cutoff to
<0.4. This filtering significantly reduced number of pairs for the
construction of regulatory network. Finally, from the selected
DEM-DEG and DETF-DEG pairs, we constructed and visualized
a composite highly differentially regulated co-expression network
for each clinical stage of prostate cancer progression using Cytos-
cape [13] as shown in Fig. 10. The number of nodes in theMAOBEGR1SNAI2MYCITGA3ZFP36GDF15miR-22*miR-575ZEB1ACTA2DESFBXO32TEAD1miR-200cmiR-627miR-548c-3p
miR-629
miR-25 GLI3BCL2ATP1B1
EDNRATP63PGRmiR-135a*HOXD10miR-32
IGFBP3
miR-375miR-19amiR-19b miR-20a*ELF1 miR-663
miR-494 miR-665miR-218 miR-145BIRC5miR-512-3p
BHLHE40CYR61 SERPINA3
IL6ST
miR-671-5pEPAS1 MEIS1 PROS1IGFBP4 PTGDS STAT3 SOCS3 PTTG1HLA-B ZEB1GBP1CEACAM1
miR-30d SNAI2miR-371-5p MMP2
JUNBITGA5PTGS2 FOSTHBS1 let-7a*
IRF1miR-1237
KITmiR-1228ID2BTG2
NFIAFBXO32TGFBR2
ZFP36
ETS2ATF3
FOSBmiR-769-5p
LDLREGR1SELENR4A2miR-125a-3pJUNTSC22D1
miR-377NR4A1miR-205miR-33bmiR-143miR-29bmiR-27bNFIBmiR-29aITGA6CCL2let-7eTOP2A
miR-28-5pARBRIP1BRCA1EZH2
miR-199a-5pE2F5CDK1miR-1SMAD9NDRG2CDC6MYBL2 FOXM1KLF4SMAD4SEPP1TP63RGS2
GADD45B
CTGFGDF15CEBPDmiR-30c miR-29cKRT14(b)(a)-1.50 1.50log2 fold changeFig. 10Integrative network constructed using significant pairs of differentially expressed gene, transcription
factors, and miRNAs based on the co-expression correlation of connected nodes for (a) primary; and (b)
metastatic prostate cancer phenotype. MiRNA, genes, and TFs are represented as oval, hexagonal, and
diamond shape nodes respectively. Nodes are colored based on their log2 fold change expression values
(green: down-regulated;red: up-regulated). Edge color indicates type of regulation (red: activation;blue:
suppression) and edge width is proportional to the absolute correlation coefficient for the expression values of
connected pairs
266 Faiz M. Khan et al.