This regulatory network was inferred from the input dataset. The miRNAs and mRNAs are
presented as round and rectangle nodes respectively. The numerical value popped up upon mouse over the gene node is the log2 transformed fold-change of the gene expression between the two groups. All of the nodes are clickable, and the detailed information of the miRNAs/mRNAs and related cancer pathway will be displayed in another window. The edges between nodes are supported by both interactions (predicted or experimentally verified) and correlations learnt from cancer dataset. The numerical value popped up upon mouse over the edge is the correlation beat value (effect size) between the two nodes. The experimental evidences of the edges reported in previous cancer studies are highlighted by red/orange color. All of these information can be accessed by the "mouse-over" action. This network shows a full map of the miRNA-mRNA regulation of the input gene list(s), and the hub miRNAs (with the high network degree/betweenness centrality) would be the potential cancer drivers or tumor suppressors. The full result table can be accessed in the "Regulations" tab.
"miRNACancerMAP" is also a network visualization tool for users to draw their regulatory network by personal customization. Users can set the complexity of the network by limiting the number of nodes or edges. And the color of the nodes can be defined by different categories of the mRNAs and miRNAs, such as Gene-Ontology, pathway, and expression status. Users can also select to use network degree or network betweenness centrality to define the node size. And edges can be black or colored by the correlation. Purple edge means negative correlation (mostly found between miRNA and mRNA), and blue edge means positive correlation (found in PPI or miRNA-miRNA sponge effect). We can also add the protein-protein interactions (PPI) into the network. This result will show the cluster of genes regulated by some specific miRNAs. Additionally, miRNA-miRNA edges can be added by the "miRNA sponge" button, presenting some clusters of miRNAs that have the interactions via sponge effect.
Num | microRNA | Gene | miRNA log2FC | miRNA pvalue | Gene log2FC | Gene pvalue | Interaction | Correlation beta | Correlation P-value | PMID | Reported in cancer studies |
---|---|---|---|---|---|---|---|---|---|---|---|
1 | hsa-miR-103a-3p | SMAD7 | 0.54 | 2.0E-5 | -1.03 | 0 | miRNAWalker2 validate | -0.18 | 0.00234 | NA | |
2 | hsa-miR-106a-5p | SMAD7 | 1.39 | 6.0E-5 | -1.03 | 0 | miRNATAP | -0.13 | 0 | NA | |
3 | hsa-miR-106b-5p | SMAD7 | 1.47 | 0 | -1.03 | 0 | miRNATAP | -0.2 | 0 | 27619676; 25286029; 22286770 | MiR 106b promotes migration and invasion through enhancing EMT via downregulation of Smad 7 in Kazakh's esophageal squamous cell carcinoma; To understand the regulation between miR-106b and Smad 7 qRT-PCR and western blot were performed; Smad 7 was confirmed as a downstream target of miR-106b in our experimental setting; Our results indicated that miR-106b can promote migration and invasion of ESCC cells through enhancing EMT process via downregulation of Smad 7 suggesting that miR-106b can be a potential molecular phenotype in ESCC metastases;Smad7 which inhibits transforming growth factor-β TGF-β/Smad signaling as a target of the miR-106b family was downregulated in CD44+ cells;The miR 106b 25 cluster targets Smad7 activates TGF β signaling and induces EMT and tumor initiating cell characteristics downstream of Six1 in human breast cancer |
4 | hsa-miR-16-5p | SMAD7 | 0.75 | 0 | -1.03 | 0 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.15 | 0.00092 | NA | |
5 | hsa-miR-17-5p | SMAD7 | 2.07 | 0 | -1.03 | 0 | TargetScan; miRNATAP | -0.17 | 0 | NA | |
6 | hsa-miR-182-5p | SMAD7 | 3.22 | 0 | -1.03 | 0 | miRNATAP | -0.13 | 0 | NA | |
7 | hsa-miR-20a-5p | SMAD7 | 2.65 | 0 | -1.03 | 0 | miRNATAP | -0.13 | 0 | NA | |
8 | hsa-miR-21-3p | SMAD7 | 2.54 | 0 | -1.03 | 0 | MirTarget | -0.12 | 0.00014 | 23372687; 27185036; 26531758 | Furthermore the expression of MSH2 and SMAD7 two important molecules involving TGF-β pathway was restored following miR-21 knockdown in both MCF-7 and Hs578T breast cancer cells;MicroRNA 21 Regulates Non Small Cell Lung Cancer Cell Invasion and Chemo Sensitivity through SMAD7; We performed bioinformatics analyses on the binding of microRNA-21 miR-21 to the 3'-UTR of SMAD7 mRNA and verified the biological effects of this binding using promoter luciferase reporter assay; Furthermore expression of miR-21 was found to be inhibited by Carboplatin and bioinformatics analyses showed that miR-21 targeted the 3'-UTR of SMAD7 mRNA to inhibit its translation which was confirmed by luciferase reporter assay; Carboplatin may upregulate SMAD7 through suppression of miR-21 to inhibit TGFβ receptor signaling mediated NSCLC cell invasion;MicroRNA 21 induces breast cancer cell invasion and migration by suppressing smad7 via EGF and TGF β pathways; The present study was undertaken to determine the association of miR-21 smad7 EGF and TGF-β with breast cancer cell invasion and migration and to identify the molecular mechanisms involved using immunohistochemistry and western blot analysis; Smad7 was confirmed to be a direct target of miR-21 by luciferase reporter and western blot assays; The downregulation of smad7 by miR-21 or sismad7 enhanced EGF-dependent invasion and migration as well as TGF-β-dependent invasion and migration; The actions of miR-21 were abrogated by expressing a modified smad7 cDNA resistant to miR-21; In conclusion our results demonstrated that plasma miR-21 levels may serve as a diagnostic marker in breast cancers whereas miR-21 promotes breast cancer cell proliferation and invasion by suppressing smad7 which enhances EGF and TGF-β pathways |
9 | hsa-miR-21-5p | SMAD7 | 4.38 | 0 | -1.03 | 0 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.15 | 0 | 23372687; 27185036; 26531758 | Furthermore the expression of MSH2 and SMAD7 two important molecules involving TGF-β pathway was restored following miR-21 knockdown in both MCF-7 and Hs578T breast cancer cells;MicroRNA 21 Regulates Non Small Cell Lung Cancer Cell Invasion and Chemo Sensitivity through SMAD7; We performed bioinformatics analyses on the binding of microRNA-21 miR-21 to the 3'-UTR of SMAD7 mRNA and verified the biological effects of this binding using promoter luciferase reporter assay; Furthermore expression of miR-21 was found to be inhibited by Carboplatin and bioinformatics analyses showed that miR-21 targeted the 3'-UTR of SMAD7 mRNA to inhibit its translation which was confirmed by luciferase reporter assay; Carboplatin may upregulate SMAD7 through suppression of miR-21 to inhibit TGFβ receptor signaling mediated NSCLC cell invasion;MicroRNA 21 induces breast cancer cell invasion and migration by suppressing smad7 via EGF and TGF β pathways; The present study was undertaken to determine the association of miR-21 smad7 EGF and TGF-β with breast cancer cell invasion and migration and to identify the molecular mechanisms involved using immunohistochemistry and western blot analysis; Smad7 was confirmed to be a direct target of miR-21 by luciferase reporter and western blot assays; The downregulation of smad7 by miR-21 or sismad7 enhanced EGF-dependent invasion and migration as well as TGF-β-dependent invasion and migration; The actions of miR-21 were abrogated by expressing a modified smad7 cDNA resistant to miR-21; In conclusion our results demonstrated that plasma miR-21 levels may serve as a diagnostic marker in breast cancers whereas miR-21 promotes breast cancer cell proliferation and invasion by suppressing smad7 which enhances EGF and TGF-β pathways |
10 | hsa-miR-25-3p | SMAD7 | 0.36 | 0.01637 | -1.03 | 0 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.17 | 0.00029 | 23435373 | MicroRNA 25 functions as a potential tumor suppressor in colon cancer by targeting Smad7; Furthermore bioinformatic predictions and experimental validation were used to identify Smad7 as a direct target of miR-25; Functional reverse experiments indicated that the antitumor effects of miR-25 were probably mediated by its repression of Smad7; These results suggest that miR-25 may function as a tumor suppressor by targeting Smad7 in colon cancer |
11 | hsa-miR-590-3p | SMAD7 | 0.84 | 0.00129 | -1.03 | 0 | miRanda | -0.17 | 0 | NA | |
12 | hsa-miR-590-5p | SMAD7 | 2.07 | 0 | -1.03 | 0 | MirTarget; PITA; miRanda; miRNATAP | -0.15 | 0 | NA | |
13 | hsa-miR-671-5p | SMAD7 | 2.24 | 0 | -1.03 | 0 | PITA | -0.12 | 2.0E-5 | NA | |
14 | hsa-miR-93-5p | SMAD7 | 1.51 | 0 | -1.03 | 0 | miRNATAP | -0.18 | 0 | 25371073 | Mothers against decapentaplegic homolog 7 Smad7 as an essential molecular protein for nuclear accumulation of β-catenin in the canonical Wnt signaling pathway is predicted as a putative target gene of miR-93 by the silico method and demonstrated that it may be suppressed by targeting its 3'UTR; These findings showed that miR-93 suppresses colorectal cancer development via downregulating Wnt/β-catenin at least in part by targeting Smad7 |
15 | hsa-miR-98-5p | SMAD7 | 1.17 | 0 | -1.03 | 0 | miRNAWalker2 validate | -0.15 | 2.0E-5 | NA |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | CELL CYCLE PROCESS | 28 | 1081 | 1.807e-18 | 8.407e-15 |
2 | REGULATION OF CELL CYCLE | 26 | 949 | 1.15e-17 | 2.676e-14 |
3 | CELL CYCLE | 29 | 1316 | 2.744e-17 | 4.256e-14 |
4 | REGULATION OF CELL CYCLE PROCESS | 19 | 558 | 1.505e-14 | 1.751e-11 |
5 | DNA METABOLIC PROCESS | 21 | 758 | 2.704e-14 | 2.516e-11 |
6 | MITOTIC CELL CYCLE | 21 | 766 | 3.32e-14 | 2.575e-11 |
7 | CELL CYCLE PHASE TRANSITION | 14 | 255 | 1.126e-13 | 7.483e-11 |
8 | DNA REPAIR | 17 | 480 | 2.453e-13 | 1.427e-10 |
9 | CELLULAR RESPONSE TO DNA DAMAGE STIMULUS | 19 | 720 | 1.401e-12 | 7.244e-10 |
10 | REGULATION OF PROTEIN MODIFICATION PROCESS | 27 | 1710 | 1.677e-12 | 7.802e-10 |
11 | REGULATION OF MITOTIC CELL CYCLE | 16 | 468 | 2.355e-12 | 9.96e-10 |
12 | CHROMOSOME ORGANIZATION | 21 | 1009 | 6.638e-12 | 2.574e-09 |
13 | SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 10 | 127 | 1.359e-11 | 4.864e-09 |
14 | SIGNAL TRANSDUCTION IN RESPONSE TO DNA DAMAGE | 9 | 96 | 3.135e-11 | 1.042e-08 |
15 | REGULATION OF CELL CYCLE PHASE TRANSITION | 13 | 321 | 4.291e-11 | 1.331e-08 |
16 | REGULATION OF DNA METABOLIC PROCESS | 13 | 340 | 8.756e-11 | 2.546e-08 |
17 | ANAPHASE PROMOTING COMPLEX DEPENDENT CATABOLIC PROCESS | 8 | 77 | 1.806e-10 | 4.942e-08 |
18 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 25 | 1805 | 2.591e-10 | 6.346e-08 |
19 | PHOSPHORYLATION | 21 | 1228 | 2.572e-10 | 6.346e-08 |
20 | REGULATION OF LIGASE ACTIVITY | 9 | 130 | 4.87e-10 | 1.133e-07 |
21 | CELLULAR RESPONSE TO STRESS | 23 | 1565 | 5.557e-10 | 1.231e-07 |
22 | CELL CYCLE CHECKPOINT | 10 | 194 | 8.971e-10 | 1.897e-07 |
23 | POSITIVE REGULATION OF CELL CYCLE | 12 | 332 | 9.509e-10 | 1.922e-07 |
24 | POSITIVE REGULATION OF PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 10 | 196 | 9.913e-10 | 1.922e-07 |
25 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 25 | 1977 | 1.751e-09 | 3.259e-07 |
26 | NEGATIVE REGULATION OF NITROGEN COMPOUND METABOLIC PROCESS | 22 | 1517 | 1.92e-09 | 3.435e-07 |
27 | REGULATION OF PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 11 | 280 | 2.136e-09 | 3.681e-07 |
28 | REGULATION OF CELL CYCLE ARREST | 8 | 108 | 2.784e-09 | 4.627e-07 |
29 | CELL DIVISION | 13 | 460 | 3.491e-09 | 5.601e-07 |
30 | RESPONSE TO ABIOTIC STIMULUS | 18 | 1024 | 4.356e-09 | 6.756e-07 |
31 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 21 | 1492 | 8.553e-09 | 1.284e-06 |
32 | REGULATION OF TRANSFERASE ACTIVITY | 17 | 946 | 9.294e-09 | 1.31e-06 |
33 | POSITIVE REGULATION OF CELL CYCLE PROCESS | 10 | 247 | 9.205e-09 | 1.31e-06 |
34 | POSITIVE REGULATION OF CELL CYCLE ARREST | 7 | 85 | 1.378e-08 | 1.886e-06 |
35 | CELL CYCLE G2 M PHASE TRANSITION | 8 | 138 | 1.939e-08 | 2.578e-06 |
36 | NEGATIVE REGULATION OF PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 8 | 139 | 2.052e-08 | 2.653e-06 |
37 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 18 | 1135 | 2.152e-08 | 2.707e-06 |
38 | POSITIVE REGULATION OF GENE EXPRESSION | 22 | 1733 | 2.219e-08 | 2.717e-06 |
39 | DNA INTEGRITY CHECKPOINT | 8 | 146 | 3.015e-08 | 3.597e-06 |
40 | MITOTIC DNA INTEGRITY CHECKPOINT | 7 | 100 | 4.297e-08 | 4.998e-06 |
41 | PROTEIN PHOSPHORYLATION | 16 | 944 | 6.226e-08 | 7.065e-06 |
42 | ORGANELLE FISSION | 12 | 496 | 8.242e-08 | 9.003e-06 |
43 | POSITIVE REGULATION OF LIGASE ACTIVITY | 7 | 110 | 8.32e-08 | 9.003e-06 |
44 | PEPTIDYL AMINO ACID MODIFICATION | 15 | 841 | 8.983e-08 | 9.087e-06 |
45 | CELL CYCLE G1 S PHASE TRANSITION | 7 | 111 | 8.857e-08 | 9.087e-06 |
46 | G1 S TRANSITION OF MITOTIC CELL CYCLE | 7 | 111 | 8.857e-08 | 9.087e-06 |
47 | NEGATIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 13 | 616 | 1.09e-07 | 1.079e-05 |
48 | INTRACELLULAR SIGNAL TRANSDUCTION | 20 | 1572 | 1.148e-07 | 1.113e-05 |
49 | PROTEIN MODIFICATION BY SMALL PROTEIN CONJUGATION OR REMOVAL | 15 | 873 | 1.458e-07 | 1.384e-05 |
50 | G1 DNA DAMAGE CHECKPOINT | 6 | 73 | 1.605e-07 | 1.494e-05 |
51 | RESPONSE TO DRUG | 11 | 431 | 1.78e-07 | 1.624e-05 |
52 | POSITIVE REGULATION OF DNA METABOLIC PROCESS | 8 | 185 | 1.885e-07 | 1.687e-05 |
53 | POSITIVE REGULATION OF CELLULAR PROTEIN CATABOLIC PROCESS | 8 | 192 | 2.505e-07 | 2.2e-05 |
54 | NEGATIVE REGULATION OF GENE EXPRESSION | 19 | 1493 | 2.604e-07 | 2.244e-05 |
55 | POSITIVE REGULATION OF CELL PROLIFERATION | 14 | 814 | 4.027e-07 | 3.407e-05 |
56 | MITOTIC CELL CYCLE CHECKPOINT | 7 | 139 | 4.133e-07 | 3.434e-05 |
57 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 16 | 1087 | 4.232e-07 | 3.454e-05 |
58 | DNA REPLICATION | 8 | 208 | 4.61e-07 | 3.698e-05 |
59 | NEGATIVE REGULATION OF CELL CYCLE PROCESS | 8 | 214 | 5.719e-07 | 4.51e-05 |
60 | REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 7 | 147 | 6.039e-07 | 4.683e-05 |
61 | REGULATION OF PROTEIN CATABOLIC PROCESS | 10 | 393 | 7.003e-07 | 5.342e-05 |
62 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 20 | 1784 | 8.78e-07 | 6.589e-05 |
63 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 19 | 1618 | 8.928e-07 | 6.594e-05 |
64 | NEGATIVE REGULATION OF CELL CYCLE G1 S PHASE TRANSITION | 6 | 98 | 9.296e-07 | 6.758e-05 |
65 | RESPONSE TO RADIATION | 10 | 413 | 1.098e-06 | 7.859e-05 |
66 | REGULATION OF SIGNAL TRANSDUCTION BY P53 CLASS MEDIATOR | 7 | 162 | 1.162e-06 | 8.19e-05 |
67 | REGULATION OF PROTEIN UBIQUITINATION INVOLVED IN UBIQUITIN DEPENDENT PROTEIN CATABOLIC PROCESS | 6 | 103 | 1.246e-06 | 8.655e-05 |
68 | REGULATION OF CELL PROLIFERATION | 18 | 1496 | 1.323e-06 | 9.055e-05 |
69 | INNATE IMMUNE RESPONSE ACTIVATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 6 | 106 | 1.475e-06 | 9.753e-05 |
70 | PROTEIN POLYUBIQUITINATION | 8 | 243 | 1.488e-06 | 9.753e-05 |
71 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 19 | 1672 | 1.465e-06 | 9.753e-05 |
72 | NEGATIVE REGULATION OF CELL CYCLE | 10 | 433 | 1.68e-06 | 0.0001086 |
73 | NUCLEOTIDE EXCISION REPAIR | 6 | 113 | 2.145e-06 | 0.0001368 |
74 | MICROTUBULE CYTOSKELETON ORGANIZATION | 9 | 348 | 2.319e-06 | 0.0001458 |
75 | NEGATIVE REGULATION OF TRANSFERASE ACTIVITY | 9 | 351 | 2.488e-06 | 0.0001544 |
76 | POSITIVE REGULATION OF PROTEIN CATABOLIC PROCESS | 8 | 263 | 2.682e-06 | 0.0001642 |
77 | POSITIVE REGULATION OF PROTEOLYSIS | 9 | 363 | 3.274e-06 | 0.0001978 |
78 | MISMATCH REPAIR | 4 | 31 | 3.381e-06 | 0.0001991 |
79 | PROTEASOMAL PROTEIN CATABOLIC PROCESS | 8 | 271 | 3.348e-06 | 0.0001991 |
80 | REGULATION OF CELLULAR PROTEIN CATABOLIC PROCESS | 8 | 274 | 3.632e-06 | 0.0002112 |
81 | INTRINSIC APOPTOTIC SIGNALING PATHWAY IN RESPONSE TO DNA DAMAGE | 5 | 71 | 3.978e-06 | 0.0002285 |
82 | NEGATIVE REGULATION OF MITOTIC CELL CYCLE | 7 | 199 | 4.56e-06 | 0.0002587 |
83 | REGULATION OF RESPONSE TO STRESS | 17 | 1468 | 4.707e-06 | 0.0002639 |
84 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 14 | 1004 | 4.774e-06 | 0.0002645 |
85 | ACTIVATION OF INNATE IMMUNE RESPONSE | 7 | 204 | 5.368e-06 | 0.0002939 |
86 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 11 | 616 | 5.809e-06 | 0.0003143 |
87 | REGULATION OF RNA STABILITY | 6 | 139 | 7.124e-06 | 0.000381 |
88 | DNA RECOMBINATION | 7 | 215 | 7.573e-06 | 0.0004004 |
89 | FC EPSILON RECEPTOR SIGNALING PATHWAY | 6 | 142 | 8.053e-06 | 0.000421 |
90 | PROTEOLYSIS | 15 | 1208 | 8.422e-06 | 0.0004354 |
91 | NIK NF KAPPAB SIGNALING | 5 | 83 | 8.6e-06 | 0.0004397 |
92 | NEGATIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 6 | 146 | 9.443e-06 | 0.0004776 |
93 | REGULATION OF DNA DEPENDENT DNA REPLICATION | 4 | 41 | 1.061e-05 | 0.0005308 |
94 | MACROMOLECULAR COMPLEX ASSEMBLY | 16 | 1398 | 1.111e-05 | 0.0005497 |
95 | CHROMATIN MODIFICATION | 10 | 539 | 1.161e-05 | 0.0005685 |
96 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 19 | 1929 | 1.194e-05 | 0.0005787 |
97 | REGULATION OF DNA BINDING | 5 | 93 | 1.5e-05 | 0.0007196 |
98 | CENTROSOME CYCLE | 4 | 45 | 1.545e-05 | 0.0007297 |
99 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 11 | 684 | 1.553e-05 | 0.0007297 |
100 | SOMATIC DIVERSIFICATION OF IMMUNE RECEPTORS VIA SOMATIC MUTATION | 3 | 15 | 1.589e-05 | 0.0007318 |
101 | DNA DAMAGE RESPONSE SIGNAL TRANSDUCTION RESULTING IN TRANSCRIPTION | 3 | 15 | 1.589e-05 | 0.0007318 |
102 | REGULATION OF DNA REPLICATION | 6 | 161 | 1.649e-05 | 0.0007522 |
103 | REGULATION OF MICROTUBULE BASED PROCESS | 7 | 243 | 1.677e-05 | 0.0007565 |
104 | POSITIVE REGULATION OF IMMUNE RESPONSE | 10 | 563 | 1.691e-05 | 0.0007565 |
105 | POSITIVE REGULATION OF INNATE IMMUNE RESPONSE | 7 | 246 | 1.815e-05 | 0.0008041 |
106 | DOUBLE STRAND BREAK REPAIR | 6 | 165 | 1.895e-05 | 0.0008318 |
107 | PURINE CONTAINING COMPOUND SALVAGE | 3 | 16 | 1.95e-05 | 0.0008403 |
108 | COVALENT CHROMATIN MODIFICATION | 8 | 345 | 1.944e-05 | 0.0008403 |
109 | DNA DEPENDENT DNA REPLICATION | 5 | 99 | 2.033e-05 | 0.0008678 |
110 | PROTEIN CATABOLIC PROCESS | 10 | 579 | 2.15e-05 | 0.0009096 |
111 | REGULATION OF PROTEOLYSIS | 11 | 711 | 2.222e-05 | 0.0009312 |
112 | REGULATION OF INNATE IMMUNE RESPONSE | 8 | 357 | 2.483e-05 | 0.001032 |
113 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 18 | 1848 | 2.523e-05 | 0.001039 |
114 | MITOTIC NUCLEAR DIVISION | 8 | 361 | 2.689e-05 | 0.001097 |
115 | AGING | 7 | 264 | 2.854e-05 | 0.00115 |
116 | REGULATION OF CATABOLIC PROCESS | 11 | 731 | 2.867e-05 | 0.00115 |
117 | POSTREPLICATION REPAIR | 4 | 54 | 3.207e-05 | 0.001264 |
118 | NEGATIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 11 | 740 | 3.206e-05 | 0.001264 |
119 | CHROMOSOME SEGREGATION | 7 | 272 | 3.453e-05 | 0.001339 |
120 | REGULATION OF CELL DIVISION | 7 | 272 | 3.453e-05 | 0.001339 |
121 | CIRCADIAN REGULATION OF GENE EXPRESSION | 4 | 57 | 3.975e-05 | 0.001529 |
122 | PROTEIN UBIQUITINATION | 10 | 629 | 4.344e-05 | 0.001657 |
123 | SOMATIC RECOMBINATION OF IMMUNOGLOBULIN GENE SEGMENTS | 3 | 21 | 4.577e-05 | 0.001731 |
124 | TUMOR NECROSIS FACTOR MEDIATED SIGNALING PATHWAY | 5 | 118 | 4.735e-05 | 0.001777 |
125 | POSITIVE REGULATION OF CATABOLIC PROCESS | 8 | 395 | 5.085e-05 | 0.001883 |
126 | NEGATIVE REGULATION OF MOLECULAR FUNCTION | 13 | 1079 | 5.098e-05 | 0.001883 |
127 | POSITIVE REGULATION OF MITOTIC CELL CYCLE | 5 | 123 | 5.773e-05 | 0.002115 |
128 | MICROTUBULE BASED PROCESS | 9 | 522 | 5.841e-05 | 0.002123 |
129 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 8 | 404 | 5.956e-05 | 0.002148 |
130 | NUCLEOTIDE EXCISION REPAIR DNA DAMAGE RECOGNITION | 3 | 23 | 6.066e-05 | 0.002171 |
131 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 17 | 1791 | 6.238e-05 | 0.002216 |
132 | RESPONSE TO UV | 5 | 126 | 6.475e-05 | 0.002282 |
133 | FC RECEPTOR SIGNALING PATHWAY | 6 | 206 | 6.568e-05 | 0.002297 |
134 | INTERSPECIES INTERACTION BETWEEN ORGANISMS | 10 | 662 | 6.665e-05 | 0.002297 |
135 | SYMBIOSIS ENCOMPASSING MUTUALISM THROUGH PARASITISM | 10 | 662 | 6.665e-05 | 0.002297 |
136 | CHROMATIN ORGANIZATION | 10 | 663 | 6.75e-05 | 0.002309 |
137 | NEGATIVE REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 4 | 66 | 7.09e-05 | 0.002373 |
138 | NUCLEOBASE CONTAINING SMALL MOLECULE METABOLIC PROCESS | 9 | 535 | 7.054e-05 | 0.002373 |
139 | NEGATIVE REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 4 | 66 | 7.09e-05 | 0.002373 |
140 | POSITIVE REGULATION OF CELL CYCLE PHASE TRANSITION | 4 | 68 | 7.972e-05 | 0.002649 |
141 | PEPTIDYL LYSINE MODIFICATION | 7 | 312 | 8.203e-05 | 0.002705 |
142 | PROTEIN COMPLEX BIOGENESIS | 13 | 1132 | 8.314e-05 | 0.002705 |
143 | PROTEIN COMPLEX ASSEMBLY | 13 | 1132 | 8.314e-05 | 0.002705 |
144 | MITOTIC SPINDLE ORGANIZATION | 4 | 69 | 8.441e-05 | 0.002709 |
145 | REGULATION OF CELL DEATH | 15 | 1472 | 8.44e-05 | 0.002709 |
146 | NEGATIVE REGULATION OF CYTOSKELETON ORGANIZATION | 6 | 221 | 9.677e-05 | 0.003084 |
147 | TRANSCRIPTION COUPLED NUCLEOTIDE EXCISION REPAIR | 4 | 73 | 0.0001052 | 0.00333 |
148 | NON CANONICAL WNT SIGNALING PATHWAY | 5 | 140 | 0.0001066 | 0.003352 |
149 | NUCLEOTIDE BINDING DOMAIN LEUCINE RICH REPEAT CONTAINING RECEPTOR SIGNALING PATHWAY | 3 | 28 | 0.0001109 | 0.003442 |
150 | DNA SYNTHESIS INVOLVED IN DNA REPAIR | 4 | 74 | 0.0001109 | 0.003442 |
151 | NUCLEAR CHROMOSOME SEGREGATION | 6 | 228 | 0.0001148 | 0.003538 |
152 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 15 | 1518 | 0.0001192 | 0.003649 |
153 | REGULATION OF IMMUNE RESPONSE | 11 | 858 | 0.000121 | 0.00368 |
154 | SOMATIC DIVERSIFICATION OF IMMUNOGLOBULINS | 3 | 29 | 0.0001234 | 0.00368 |
155 | POSTTRANSCRIPTIONAL REGULATION OF GENE EXPRESSION | 8 | 448 | 0.0001221 | 0.00368 |
156 | DNA REPLICATION INITIATION | 3 | 29 | 0.0001234 | 0.00368 |
157 | RESPONSE TO IONIZING RADIATION | 5 | 145 | 0.0001258 | 0.003727 |
158 | T CELL RECEPTOR SIGNALING PATHWAY | 5 | 146 | 0.0001299 | 0.003801 |
159 | RESPONSE TO TUMOR NECROSIS FACTOR | 6 | 233 | 0.0001293 | 0.003801 |
160 | POSITIVE REGULATION OF IMMUNE SYSTEM PROCESS | 11 | 867 | 0.0001327 | 0.003858 |
161 | NEGATIVE REGULATION OF RESPONSE TO STIMULUS | 14 | 1360 | 0.0001368 | 0.003954 |
162 | NUCLEOSIDE MONOPHOSPHATE METABOLIC PROCESS | 6 | 239 | 0.0001485 | 0.004264 |
163 | INTRINSIC APOPTOTIC SIGNALING PATHWAY | 5 | 152 | 0.0001569 | 0.004451 |
164 | MEIOTIC CELL CYCLE PROCESS | 5 | 152 | 0.0001569 | 0.004451 |
165 | REGULATION OF CENTROSOME DUPLICATION | 3 | 32 | 0.0001663 | 0.004688 |
166 | SOMATIC CELL DNA RECOMBINATION | 3 | 33 | 0.0001824 | 0.005023 |
167 | SOMATIC DIVERSIFICATION OF IMMUNE RECEPTORS VIA GERMLINE RECOMBINATION WITHIN A SINGLE LOCUS | 3 | 33 | 0.0001824 | 0.005023 |
168 | MICROTUBULE ORGANIZING CENTER ORGANIZATION | 4 | 84 | 0.0001814 | 0.005023 |
169 | CYTOPLASMIC PATTERN RECOGNITION RECEPTOR SIGNALING PATHWAY | 3 | 33 | 0.0001824 | 0.005023 |
170 | RESPONSE TO PURINE CONTAINING COMPOUND | 5 | 158 | 0.0001879 | 0.005144 |
171 | POSITIVE REGULATION OF DNA REPLICATION | 4 | 86 | 0.0001987 | 0.005406 |
172 | REGULATION OF NUCLEAR DIVISION | 5 | 163 | 0.0002172 | 0.005694 |
173 | REGULATION OF CELLULAR AMINE METABOLIC PROCESS | 4 | 88 | 0.0002171 | 0.005694 |
174 | MEIOSIS I | 4 | 88 | 0.0002171 | 0.005694 |
175 | RESPONSE TO ORGANIC CYCLIC COMPOUND | 11 | 917 | 0.0002163 | 0.005694 |
176 | NEGATIVE REGULATION OF CANONICAL WNT SIGNALING PATHWAY | 5 | 162 | 0.0002111 | 0.005694 |
177 | POSITIVE REGULATION OF DEFENSE RESPONSE | 7 | 364 | 0.0002126 | 0.005694 |
178 | RESPONSE TO IRON ION | 3 | 35 | 0.0002178 | 0.005694 |
179 | GLYCOSYL COMPOUND METABOLIC PROCESS | 7 | 368 | 0.0002272 | 0.005906 |
180 | REGULATION OF KINASE ACTIVITY | 10 | 776 | 0.0002443 | 0.006315 |
181 | INTRACELLULAR RECEPTOR SIGNALING PATHWAY | 5 | 168 | 0.0002499 | 0.006424 |
182 | POSITIVE REGULATION OF DNA REPAIR | 3 | 38 | 0.0002787 | 0.007087 |
183 | CELLULAR METABOLIC COMPOUND SALVAGE | 3 | 38 | 0.0002787 | 0.007087 |
184 | REGULATION OF CENTROSOME CYCLE | 3 | 39 | 0.0003012 | 0.007618 |
185 | NEGATIVE REGULATION OF ORGANELLE ORGANIZATION | 7 | 387 | 0.0003083 | 0.007755 |
186 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 10 | 801 | 0.0003146 | 0.007847 |
187 | REGULATION OF CYCLIN DEPENDENT PROTEIN KINASE ACTIVITY | 4 | 97 | 0.0003153 | 0.007847 |
188 | REGULATION OF TRANSFORMING GROWTH FACTOR BETA RECEPTOR SIGNALING PATHWAY | 4 | 99 | 0.0003409 | 0.008392 |
189 | REGULATION OF CELLULAR RESPONSE TO TRANSFORMING GROWTH FACTOR BETA STIMULUS | 4 | 99 | 0.0003409 | 0.008392 |
190 | PURINE CONTAINING COMPOUND METABOLIC PROCESS | 7 | 394 | 0.0003435 | 0.008412 |
191 | MITOTIC SPINDLE ASSEMBLY | 3 | 41 | 0.0003497 | 0.008431 |
192 | MICROTUBULE CYTOSKELETON ORGANIZATION INVOLVED IN MITOSIS | 3 | 41 | 0.0003497 | 0.008431 |
193 | RESPONSE TO LIGHT STIMULUS | 6 | 280 | 0.0003482 | 0.008431 |
194 | SOMATIC DIVERSIFICATION OF IMMUNE RECEPTORS | 3 | 42 | 0.0003757 | 0.009011 |
195 | NEGATIVE REGULATION OF TRANSMEMBRANE RECEPTOR PROTEIN SERINE THREONINE KINASE SIGNALING PATHWAY | 4 | 102 | 0.0003819 | 0.009114 |
196 | MEIOTIC CELL CYCLE | 5 | 186 | 0.0003992 | 0.009477 |
197 | NEGATIVE REGULATION OF CATALYTIC ACTIVITY | 10 | 829 | 0.0004128 | 0.009751 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | ENZYME BINDING | 28 | 1737 | 3.224e-13 | 2.995e-10 |
2 | KINASE BINDING | 14 | 606 | 1.055e-08 | 4.901e-06 |
3 | PROTEIN COMPLEX BINDING | 16 | 935 | 5.455e-08 | 1.296e-05 |
4 | MISMATCHED DNA BINDING | 4 | 12 | 5.579e-08 | 1.296e-05 |
5 | MACROMOLECULAR COMPLEX BINDING | 19 | 1399 | 9.433e-08 | 1.753e-05 |
6 | DOUBLE STRANDED DNA BINDING | 14 | 764 | 1.869e-07 | 2.894e-05 |
7 | DAMAGED DNA BINDING | 5 | 63 | 2.192e-06 | 0.0002909 |
8 | SEQUENCE SPECIFIC DNA BINDING | 14 | 1037 | 6.919e-06 | 0.0008035 |
9 | IDENTICAL PROTEIN BINDING | 15 | 1209 | 8.506e-06 | 0.000878 |
10 | REGULATORY REGION NUCLEIC ACID BINDING | 12 | 818 | 1.527e-05 | 0.00129 |
11 | SINGLE STRANDED DNA BINDING | 5 | 93 | 1.5e-05 | 0.00129 |
12 | ADENYL NUCLEOTIDE BINDING | 16 | 1514 | 2.982e-05 | 0.002308 |
13 | RNA BINDING | 16 | 1598 | 5.736e-05 | 0.004099 |
14 | KINASE ACTIVITY | 11 | 842 | 0.0001025 | 0.006348 |
15 | RIBONUCLEOTIDE BINDING | 17 | 1860 | 9.984e-05 | 0.006348 |
16 | TRANSCRIPTION FACTOR ACTIVITY PROTEIN BINDING | 9 | 588 | 0.0001444 | 0.007893 |
17 | NF KAPPAB BINDING | 3 | 30 | 0.0001367 | 0.007893 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | CHROMOSOME | 19 | 880 | 4.543e-11 | 2.653e-08 |
2 | NUCLEAR CHROMOSOME | 13 | 523 | 1.61e-08 | 4.701e-06 |
3 | CHROMOSOMAL REGION | 10 | 330 | 1.407e-07 | 2.74e-05 |
4 | CONDENSED CHROMOSOME | 8 | 195 | 2.821e-07 | 4.118e-05 |
5 | CHROMOSOME TELOMERIC REGION | 7 | 162 | 1.162e-06 | 0.0001357 |
6 | MISMATCH REPAIR COMPLEX | 3 | 14 | 1.274e-05 | 0.00124 |
7 | CENTROSOME | 9 | 487 | 3.412e-05 | 0.002847 |
8 | MICROTUBULE ORGANIZING CENTER | 10 | 623 | 4.007e-05 | 0.002925 |
9 | NUCLEAR CHROMOSOME TELOMERIC REGION | 5 | 132 | 8.075e-05 | 0.00524 |
10 | TRANSFERASE COMPLEX | 10 | 703 | 0.0001096 | 0.006165 |
11 | NUCLEOPLASM PART | 10 | 708 | 0.0001161 | 0.006165 |
12 | CATALYTIC COMPLEX | 12 | 1038 | 0.0001525 | 0.007423 |
13 | CONDENSED NUCLEAR CHROMOSOME | 4 | 85 | 0.0001899 | 0.008295 |
14 | MICROTUBULE CYTOSKELETON | 12 | 1068 | 0.0001989 | 0.008295 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | Cell_cycle_hsa04110 | 11 | 124 | 3.175e-13 | 1.651e-11 | |
2 | Cellular_senescence_hsa04218 | 11 | 160 | 5.305e-12 | 1.379e-10 | |
3 | p53_signaling_pathway_hsa04115 | 5 | 68 | 3.21e-06 | 5.563e-05 | |
4 | Oocyte_meiosis_hsa04114 | 5 | 124 | 6e-05 | 0.00078 | |
5 | FoxO_signaling_pathway_hsa04068 | 5 | 132 | 8.075e-05 | 0.0008398 | |
6 | Notch_signaling_pathway_hsa04330 | 3 | 48 | 0.000558 | 0.004836 | |
7 | PI3K_Akt_signaling_pathway_hsa04151 | 6 | 352 | 0.001152 | 0.008558 | |
8 | HIF_1_signaling_pathway_hsa04066 | 3 | 100 | 0.004609 | 0.02996 | |
9 | Regulation_of_actin_cytoskeleton_hsa04810 | 4 | 208 | 0.005226 | 0.03019 | |
10 | Hippo_signaling_pathway_hsa04390 | 3 | 154 | 0.01497 | 0.07786 | |
11 | TGF_beta_signaling_pathway_hsa04350 | 2 | 84 | 0.03231 | 0.1528 | |
12 | Endocytosis_hsa04144 | 3 | 244 | 0.04859 | 0.2036 | |
13 | TNF_signaling_pathway_hsa04668 | 2 | 108 | 0.0509 | 0.2036 | |
14 | Autophagy_animal_hsa04140 | 2 | 128 | 0.06865 | 0.2541 | |
15 | MAPK_signaling_pathway_hsa04010 | 3 | 295 | 0.07647 | 0.2541 | |
16 | Apoptosis_hsa04210 | 2 | 138 | 0.07818 | 0.2541 | |
17 | mTOR_signaling_pathway_hsa04150 | 2 | 151 | 0.09115 | 0.2788 | |
18 | Rap1_signaling_pathway_hsa04015 | 2 | 206 | 0.1516 | 0.3942 |
Num | lncRNA | miRNAs | miRNAs count | Gene | Sponge regulatory network | lncRNA log2FC | lncRNA pvalue | Gene log2FC | Gene pvalue | lncRNA-gene Pearson correlation |
---|---|---|---|---|---|---|---|---|---|---|
1 | TBX5-AS1 | hsa-miR-103a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-5p | 10 | SMAD7 | Sponge network | -2.108 | 0 | -1.033 | 0 | 0.448 |
2 | RP11-401P9.4 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-98-5p | 12 | SMAD7 | Sponge network | -3.04 | 0 | -1.033 | 0 | 0.437 |
3 | RP11-389C8.2 | hsa-miR-103a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-590-3p;hsa-miR-671-5p;hsa-miR-93-5p | 11 | SMAD7 | Sponge network | -2.039 | 0 | -1.033 | 0 | 0.423 |
4 | AC109642.1 | hsa-miR-103a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-93-5p;hsa-miR-98-5p | 13 | SMAD7 | Sponge network | -2.791 | 0 | -1.033 | 0 | 0.421 |
5 | LINC00702 | hsa-miR-103a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-671-5p;hsa-miR-93-5p | 14 | SMAD7 | Sponge network | -2.856 | 0 | -1.033 | 0 | 0.388 |
6 | RP11-456K23.1 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p | 12 | SMAD7 | Sponge network | -1.488 | 0 | -1.033 | 0 | 0.383 |
7 | RP11-1024P17.1 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p | 10 | SMAD7 | Sponge network | -2.062 | 0 | -1.033 | 0 | 0.371 |
8 | LINC00968 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-671-5p;hsa-miR-93-5p | 12 | SMAD7 | Sponge network | -4.19 | 0 | -1.033 | 0 | 0.36 |
9 | MAGI2-AS3 | hsa-miR-103a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-671-5p;hsa-miR-93-5p | 13 | SMAD7 | Sponge network | -1.892 | 0 | -1.033 | 0 | 0.353 |
10 | MIR497HG | hsa-miR-103a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-5p;hsa-miR-671-5p;hsa-miR-93-5p | 13 | SMAD7 | Sponge network | -2.142 | 0 | -1.033 | 0 | 0.352 |
11 | CTD-2013N24.2 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-93-5p | 10 | SMAD7 | Sponge network | -1.745 | 0 | -1.033 | 0 | 0.336 |
12 | FENDRR | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-671-5p;hsa-miR-93-5p;hsa-miR-98-5p | 13 | SMAD7 | Sponge network | -4.222 | 0 | -1.033 | 0 | 0.334 |
13 | DNM3OS | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p | 10 | SMAD7 | Sponge network | 0.053 | 0.85755 | -1.033 | 0 | 0.33 |
14 | LL22NC03-86G7.1 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-93-5p;hsa-miR-98-5p | 12 | SMAD7 | Sponge network | -1.177 | 3.0E-5 | -1.033 | 0 | 0.32 |
15 | BAIAP2-AS1 | hsa-miR-103a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-671-5p;hsa-miR-93-5p | 10 | SMAD7 | Sponge network | -0.182 | 0.51705 | -1.033 | 0 | 0.301 |
16 | LINC00261 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-590-5p;hsa-miR-671-5p | 11 | SMAD7 | Sponge network | -2.566 | 0.00025 | -1.033 | 0 | 0.283 |
17 | AC007743.1 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-590-5p;hsa-miR-671-5p;hsa-miR-93-5p | 10 | SMAD7 | Sponge network | -2.595 | 0 | -1.033 | 0 | 0.268 |
18 | RP11-536K7.3 | hsa-miR-103a-3p;hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-93-5p | 11 | SMAD7 | Sponge network | -1.239 | 5.0E-5 | -1.033 | 0 | 0.266 |
19 | AC079630.4 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-671-5p;hsa-miR-93-5p | 10 | SMAD7 | Sponge network | -3.758 | 0 | -1.033 | 0 | 0.259 |
20 | RP11-354E11.2 | hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-20a-5p;hsa-miR-21-5p;hsa-miR-25-3p;hsa-miR-590-3p;hsa-miR-671-5p | 10 | SMAD7 | Sponge network | -2.138 | 0 | -1.033 | 0 | 0.258 |