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-106a-5p | AKT3 | -0.2 | 0.80221 | 0.46 | 0.53933 | miRNATAP | -0.55 | 0 | NA | |
2 | hsa-miR-106b-5p | AKT3 | -0.3 | 0.86929 | 0.46 | 0.53933 | miRNATAP | -0.91 | 0 | NA | |
3 | hsa-miR-107 | AKT3 | -0.04 | 0.98836 | 0.46 | 0.53933 | PITA; miRanda | -0.55 | 0.00017 | NA | |
4 | hsa-miR-1275 | AKT3 | -0.83 | 0.08038 | 0.46 | 0.53933 | PITA | -0.27 | 0 | NA | |
5 | hsa-miR-142-3p | AKT3 | -0.15 | 0.9461 | 0.46 | 0.53933 | miRanda | -0.2 | 0.00627 | NA | |
6 | hsa-miR-15a-5p | AKT3 | -0.07 | 0.96484 | 0.46 | 0.53933 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.72 | 0 | NA | |
7 | hsa-miR-15b-5p | AKT3 | -0.27 | 0.87097 | 0.46 | 0.53933 | miRNATAP | -0.67 | 0 | NA | |
8 | hsa-miR-16-5p | AKT3 | 0.01 | 0.99448 | 0.46 | 0.53933 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.75 | 0 | NA | |
9 | hsa-miR-17-3p | AKT3 | 0.1 | 0.96011 | 0.46 | 0.53933 | miRNATAP | -0.52 | 0 | NA | |
10 | hsa-miR-17-5p | AKT3 | -0.18 | 0.93454 | 0.46 | 0.53933 | TargetScan; miRNATAP | -0.63 | 0 | NA | |
11 | hsa-miR-181b-5p | AKT3 | 0.16 | 0.93018 | 0.46 | 0.53933 | miRNATAP | -0.27 | 0.00963 | NA | |
12 | hsa-miR-20a-5p | AKT3 | -0.18 | 0.92812 | 0.46 | 0.53933 | miRNATAP | -0.53 | 0 | NA | |
13 | hsa-miR-28-3p | AKT3 | -0.23 | 0.93535 | 0.46 | 0.53933 | miRNATAP | -0.52 | 0.00719 | NA | |
14 | hsa-miR-29a-3p | AKT3 | 0.01 | 0.99698 | 0.46 | 0.53933 | miRNATAP | -0.81 | 0 | NA | |
15 | hsa-miR-29b-3p | AKT3 | -0.1 | 0.95899 | 0.46 | 0.53933 | miRNATAP | -0.68 | 0 | 26512921 | MicroRNA 29B mir 29b regulates the Warburg effect in ovarian cancer by targeting AKT2 and AKT3 |
16 | hsa-miR-32-3p | AKT3 | -0.57 | 0.13133 | 0.46 | 0.53933 | mirMAP | -0.56 | 0 | NA | |
17 | hsa-miR-320a | AKT3 | -0.42 | 0.8402 | 0.46 | 0.53933 | PITA; miRanda; miRNATAP | -0.33 | 0.00138 | NA | |
18 | hsa-miR-320b | AKT3 | -0.24 | 0.85922 | 0.46 | 0.53933 | PITA; miRanda; miRNATAP | -0.25 | 0.00855 | NA | |
19 | hsa-miR-335-3p | AKT3 | -0.24 | 0.8845 | 0.46 | 0.53933 | mirMAP | -0.58 | 0 | NA | |
20 | hsa-miR-33a-3p | AKT3 | -0.79 | 0.01052 | 0.46 | 0.53933 | mirMAP | -0.49 | 0 | NA | |
21 | hsa-miR-340-5p | AKT3 | -0 | 0.99757 | 0.46 | 0.53933 | mirMAP | -0.28 | 0.006 | NA | |
22 | hsa-miR-362-3p | AKT3 | -0.72 | 0.03459 | 0.46 | 0.53933 | miRanda | -0.42 | 0 | NA | |
23 | hsa-miR-362-5p | AKT3 | -0.27 | 0.75202 | 0.46 | 0.53933 | PITA; TargetScan; miRNATAP | -0.52 | 0 | NA | |
24 | hsa-miR-369-3p | AKT3 | 0.12 | 0.8323 | 0.46 | 0.53933 | mirMAP | -0.23 | 0.00901 | NA | |
25 | hsa-miR-374a-5p | AKT3 | -0.34 | 0.76692 | 0.46 | 0.53933 | mirMAP | -0.58 | 0 | NA | |
26 | hsa-miR-374b-5p | AKT3 | -0.29 | 0.8357 | 0.46 | 0.53933 | mirMAP | -0.68 | 0 | NA | |
27 | hsa-miR-421 | AKT3 | -0.18 | 0.7347 | 0.46 | 0.53933 | miRanda; mirMAP | -0.46 | 0 | NA | |
28 | hsa-miR-424-5p | AKT3 | 0.25 | 0.87015 | 0.46 | 0.53933 | miRNATAP | -0.24 | 0.00104 | 26315541 | Silencing Akt3 and E2F3 by siRNA pheno-copied the effect of ectopic miR-424 on HCC growth; Whereas overexpression of Akt3 and E2F3 attenuated the effect of miR-424 on HCC growth |
29 | hsa-miR-501-3p | AKT3 | -0.75 | 0.55276 | 0.46 | 0.53933 | miRNATAP | -0.5 | 0 | NA | |
30 | hsa-miR-502-3p | AKT3 | -0.48 | 0.5143 | 0.46 | 0.53933 | miRNATAP | -0.64 | 0 | NA | |
31 | hsa-miR-502-5p | AKT3 | -0.71 | 0.02613 | 0.46 | 0.53933 | PITA; miRNATAP | -0.41 | 0 | NA | |
32 | hsa-miR-505-3p | AKT3 | -0.47 | 0.69038 | 0.46 | 0.53933 | mirMAP | -0.77 | 0 | 22051041 | We also find that Akt3 correlate inversely with miR-505 modulates drug sensitivity in MCF7-ADR |
33 | hsa-miR-548o-3p | AKT3 | -0.19 | 0.51773 | 0.46 | 0.53933 | mirMAP | -0.31 | 8.0E-5 | NA | |
34 | hsa-miR-577 | AKT3 | -1.06 | 0.32606 | 0.46 | 0.53933 | mirMAP | -0.38 | 0 | NA | |
35 | hsa-miR-663b | AKT3 | 0.1 | 0.81499 | 0.46 | 0.53933 | PITA | -0.25 | 1.0E-5 | NA | |
36 | hsa-miR-769-5p | AKT3 | -0.31 | 0.7357 | 0.46 | 0.53933 | PITA; miRNATAP | -0.84 | 0 | NA | |
37 | hsa-miR-93-5p | AKT3 | -0.61 | 0.8253 | 0.46 | 0.53933 | miRNATAP | -0.76 | 0 | NA | |
38 | hsa-miR-146b-5p | BRAF | -0.4 | 0.83751 | -0.04 | 0.94896 | miRanda | -0.12 | 0.00232 | 21874046; 26883911; 20406109; 21537871 | Additionally the activation of thyroid most common oncogenes RET/PTC3 and BRAF in PCCL3 cells upregulated miR-146b-5p expression;miR-146b-5p positively regulates migration and invasion of thyroid normal and tumor follicular cells independently from their original mutation either BRAF or RET/PTC through a mechanism that involves the actin cytoskeleton but not an increased capacity of matrix degradation;The miR-146b expression levels in PTCs with BRAF mutation were significantly higher than those without this mutation p < 0.0001;Among BRAF-positive tumors overexpression of miR-146b was associated with aggressive behavior suggesting that it may further refine the prognostic importance of BRAF |
39 | hsa-miR-199a-5p | BRAF | 0.16 | 0.9358 | -0.04 | 0.94896 | miRanda | -0.1 | 0.00848 | NA | |
40 | hsa-miR-199b-5p | BRAF | -0.04 | 0.97717 | -0.04 | 0.94896 | miRanda | -0.12 | 0.0002 | NA | |
41 | hsa-miR-539-5p | CAB39 | 0.12 | 0.80107 | -0.14 | 0.92657 | mirMAP | -0.11 | 1.0E-5 | NA | |
42 | hsa-miR-155-5p | CAB39L | -0.41 | 0.82867 | 0.88 | 0.38138 | miRNAWalker2 validate | -0.57 | 0 | NA | |
43 | hsa-miR-342-3p | CAB39L | -0.37 | 0.77314 | 0.88 | 0.38138 | miRanda | -0.35 | 0.00145 | NA | |
44 | hsa-miR-582-5p | CAB39L | -0.4 | 0.58123 | 0.88 | 0.38138 | miRNATAP | -0.68 | 0 | NA | |
45 | hsa-miR-590-3p | CAB39L | -0.28 | 0.59127 | 0.88 | 0.38138 | miRanda | -0.33 | 0.00021 | NA | |
46 | hsa-miR-7-1-3p | CAB39L | -0.46 | 0.6659 | 0.88 | 0.38138 | mirMAP | -0.35 | 0.00083 | NA | |
47 | hsa-miR-101-3p | DDIT4 | 0.01 | 0.99704 | 0.41 | 0.80745 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.33 | 0.00086 | NA | |
48 | hsa-miR-181d-5p | DDIT4 | 0.15 | 0.888 | 0.41 | 0.80745 | MirTarget | -0.15 | 0.00566 | NA | |
49 | hsa-miR-217 | DDIT4 | 0.34 | 0.761 | 0.41 | 0.80745 | miRanda | -0.2 | 6.0E-5 | NA | |
50 | hsa-miR-195-5p | EIF4B | 0.34 | 0.74962 | -0.02 | 0.99375 | MirTarget; miRNATAP | -0.1 | 0.00113 | NA | |
51 | hsa-miR-497-5p | EIF4B | -0.01 | 0.98915 | -0.02 | 0.99375 | miRNATAP | -0.14 | 0.00012 | NA | |
52 | hsa-miR-130a-3p | EIF4E | 0.09 | 0.9291 | -0.02 | 0.98745 | mirMAP | -0.12 | 0.00106 | NA | |
53 | hsa-miR-139-5p | EIF4E | -0.08 | 0.92869 | -0.02 | 0.98745 | miRanda | -0.11 | 0.00314 | NA | |
54 | hsa-miR-145-5p | EIF4E | 0.04 | 0.98758 | -0.02 | 0.98745 | miRNAWalker2 validate; miRTarBase | -0.13 | 8.0E-5 | NA | |
55 | hsa-miR-29c-3p | EIF4E | 0.16 | 0.94272 | -0.02 | 0.98745 | mirMAP | -0.11 | 0.00551 | NA | |
56 | hsa-miR-30a-3p | EIF4E | 0.25 | 0.91709 | -0.02 | 0.98745 | mirMAP | -0.13 | 0.00696 | NA | |
57 | hsa-miR-485-3p | EIF4E | -0.08 | 0.84013 | -0.02 | 0.98745 | MirTarget; mirMAP | -0.11 | 0.00075 | NA | |
58 | hsa-miR-125b-5p | EIF4EBP1 | 0.04 | 0.98059 | -0.18 | 0.89152 | miRNAWalker2 validate; miRTarBase; MirTarget; miRNATAP | -0.14 | 0.00144 | 17891175; 26646586 | Using a bioinformatics approach we have identified additional potential mRNA targets of one of the miRNAs miR-125b that are upregulated in prostate cancer and confirmed increased expression of one of these targets EIF4EBP1 in prostate cancer tissues;Increased expression of miR-125a and miR-125b inhibited invasion and migration of SKOV3 and OVCAR-429 ovarian cancer cells and was associated with a decrease in EIF4EBP1 expression |
59 | hsa-miR-106a-5p | HIF1A | -0.2 | 0.80221 | -0.18 | 0.90824 | MirTarget | -0.21 | 0 | NA | |
60 | hsa-miR-106b-5p | HIF1A | -0.3 | 0.86929 | -0.18 | 0.90824 | MirTarget | -0.24 | 0 | NA | |
61 | hsa-miR-143-5p | HIF1A | 0.11 | 0.93336 | -0.18 | 0.90824 | MirTarget | -0.16 | 9.0E-5 | NA | |
62 | hsa-miR-17-5p | HIF1A | -0.18 | 0.93454 | -0.18 | 0.90824 | miRTarBase; MirTarget; TargetScan | -0.22 | 0 | NA | |
63 | hsa-miR-18a-5p | HIF1A | -0.5 | 0.61264 | -0.18 | 0.90824 | miRNAWalker2 validate; MirTarget | -0.15 | 1.0E-5 | 25069832 | Last clinically relevant correlations between miR-18a HIF1A hypoxia-responsive gene expression and distant metastasis-free survival DMFS were assessed using published expression array breast tumors data sets; We identified HIF1A as a direct target of miR-18a; Analysis of previously published data revealed that higher expression of HIF1A and a panel of hypoxic genes is associated with shorter DMFS interval in patients with basal-like breast tumors and that within this subtype miR-18a expression is inversely correlated with hypoxic gene expression; The results of this study reveal a novel role for miR-18a in targeting HIF1A and repressing metastasis of basal-like breast tumors |
64 | hsa-miR-18b-5p | HIF1A | -0.05 | 0.89998 | -0.18 | 0.90824 | MirTarget | -0.12 | 0.00029 | NA | |
65 | hsa-miR-20a-5p | HIF1A | -0.18 | 0.92812 | -0.18 | 0.90824 | miRNAWalker2 validate; miRTarBase; MirTarget | -0.19 | 0 | 22901144 | Correlation analysis showed that the key miRNAs miR-20a and miR-20b negatively correlated with the target proteins VEGF-A and HIF-1alpha |
66 | hsa-miR-28-5p | HIF1A | -0.11 | 0.9406 | -0.18 | 0.90824 | miRanda | -0.42 | 0.00044 | NA | |
67 | hsa-miR-33a-5p | HIF1A | -0.21 | 0.85331 | -0.18 | 0.90824 | miRNAWalker2 validate | -0.13 | 0 | NA | |
68 | hsa-miR-361-5p | HIF1A | -0.14 | 0.9415 | -0.18 | 0.90824 | miRanda | -0.36 | 0 | NA | |
69 | hsa-miR-424-5p | HIF1A | 0.25 | 0.87015 | -0.18 | 0.90824 | miRNAWalker2 validate; miRTarBase | -0.13 | 0.00059 | NA | |
70 | hsa-miR-660-5p | HIF1A | -0.48 | 0.69408 | -0.18 | 0.90824 | MirTarget | -0.21 | 0 | NA | |
71 | hsa-miR-93-5p | HIF1A | -0.61 | 0.8253 | -0.18 | 0.90824 | MirTarget | -0.14 | 0.00488 | NA | |
72 | hsa-let-7a-3p | IGF1 | -0.22 | 0.85543 | 0.01 | 0.98747 | mirMAP | -1.08 | 0 | NA | |
73 | hsa-let-7f-1-3p | IGF1 | -0.31 | 0.69341 | 0.01 | 0.98747 | mirMAP | -1.34 | 0 | NA | |
74 | hsa-miR-1275 | IGF1 | -0.83 | 0.08038 | 0.01 | 0.98747 | MirTarget; PITA | -0.38 | 5.0E-5 | NA | |
75 | hsa-miR-130b-3p | IGF1 | -0.22 | 0.82466 | 0.01 | 0.98747 | MirTarget | -1.33 | 0 | NA | |
76 | hsa-miR-148a-5p | IGF1 | -0.45 | 0.74842 | 0.01 | 0.98747 | mirMAP | -0.73 | 0 | NA | |
77 | hsa-miR-15b-3p | IGF1 | -0.56 | 0.60918 | 0.01 | 0.98747 | mirMAP | -1.37 | 0 | NA | |
78 | hsa-miR-16-1-3p | IGF1 | 0.15 | 0.73374 | 0.01 | 0.98747 | mirMAP | -0.87 | 0 | NA | |
79 | hsa-miR-186-5p | IGF1 | -0.32 | 0.85413 | 0.01 | 0.98747 | mirMAP | -1.35 | 0 | NA | |
80 | hsa-miR-19a-3p | IGF1 | -0.21 | 0.84464 | 0.01 | 0.98747 | MirTarget | -0.99 | 0 | NA | |
81 | hsa-miR-19b-1-5p | IGF1 | -0.01 | 0.98851 | 0.01 | 0.98747 | mirMAP | -0.96 | 0 | NA | |
82 | hsa-miR-19b-3p | IGF1 | -0.03 | 0.98666 | 0.01 | 0.98747 | MirTarget | -1.19 | 0 | NA | |
83 | hsa-miR-20a-3p | IGF1 | 0.46 | 0.57674 | 0.01 | 0.98747 | mirMAP | -0.83 | 0 | NA | |
84 | hsa-miR-224-3p | IGF1 | 0.11 | 0.74909 | 0.01 | 0.98747 | mirMAP | -0.32 | 0.00753 | NA | |
85 | hsa-miR-26b-5p | IGF1 | -0.02 | 0.99038 | 0.01 | 0.98747 | mirMAP | -1.33 | 0 | NA | |
86 | hsa-miR-27a-3p | IGF1 | -0.12 | 0.9588 | 0.01 | 0.98747 | miRNAWalker2 validate; miRTarBase | -1.33 | 0 | NA | |
87 | hsa-miR-29a-3p | IGF1 | 0.01 | 0.99698 | 0.01 | 0.98747 | MirTarget | -1.22 | 0 | NA | |
88 | hsa-miR-29b-3p | IGF1 | -0.1 | 0.95899 | 0.01 | 0.98747 | MirTarget | -1.13 | 0 | 25592039 | Luciferase reporter assays were conducted to determine the association between miR-29b and the insulin-like growth factor 1 IGF1 3' untranslated region 3'UTR; IGF1 an activator of PI3K/Akt signaling was confirmed as a novel target of miR-29b |
89 | hsa-miR-301a-3p | IGF1 | -0.11 | 0.83169 | 0.01 | 0.98747 | MirTarget | -0.72 | 0 | NA | |
90 | hsa-miR-32-3p | IGF1 | -0.57 | 0.13133 | 0.01 | 0.98747 | mirMAP | -0.85 | 0 | NA | |
91 | hsa-miR-320a | IGF1 | -0.42 | 0.8402 | 0.01 | 0.98747 | miRNATAP | -0.53 | 0.00309 | NA | |
92 | hsa-miR-33a-3p | IGF1 | -0.79 | 0.01052 | 0.01 | 0.98747 | MirTarget | -0.71 | 0 | NA | |
93 | hsa-miR-361-5p | IGF1 | -0.14 | 0.9415 | 0.01 | 0.98747 | PITA; mirMAP | -0.76 | 0.00313 | NA | |
94 | hsa-miR-362-5p | IGF1 | -0.27 | 0.75202 | 0.01 | 0.98747 | mirMAP | -0.69 | 0 | NA | |
95 | hsa-miR-369-3p | IGF1 | 0.12 | 0.8323 | 0.01 | 0.98747 | mirMAP | -0.42 | 0.00732 | NA | |
96 | hsa-miR-374b-3p | IGF1 | -0.05 | 0.86075 | 0.01 | 0.98747 | mirMAP | -0.9 | 0 | NA | |
97 | hsa-miR-376b-3p | IGF1 | -0.01 | 0.98243 | 0.01 | 0.98747 | mirMAP | -0.4 | 0.00219 | NA | |
98 | hsa-miR-377-3p | IGF1 | -0.04 | 0.89351 | 0.01 | 0.98747 | mirMAP | -0.35 | 0.00945 | NA | |
99 | hsa-miR-421 | IGF1 | -0.18 | 0.7347 | 0.01 | 0.98747 | PITA | -0.68 | 0 | NA | |
100 | hsa-miR-450b-5p | IGF1 | -0.01 | 0.98315 | 0.01 | 0.98747 | MirTarget; PITA; mirMAP; miRNATAP | -0.44 | 0.00527 | NA | |
101 | hsa-miR-452-5p | IGF1 | -0.05 | 0.97387 | 0.01 | 0.98747 | MirTarget; mirMAP | -0.39 | 0.00722 | NA | |
102 | hsa-miR-454-3p | IGF1 | -0.1 | 0.84355 | 0.01 | 0.98747 | MirTarget | -1.21 | 0 | NA | |
103 | hsa-miR-486-5p | IGF1 | -0.55 | 0.6964 | 0.01 | 0.98747 | PITA; miRNATAP | -0.28 | 0.00602 | NA | |
104 | hsa-miR-576-5p | IGF1 | -0.51 | 0.41719 | 0.01 | 0.98747 | PITA; mirMAP; miRNATAP | -1.08 | 0 | NA | |
105 | hsa-miR-577 | IGF1 | -1.06 | 0.32606 | 0.01 | 0.98747 | PITA | -0.61 | 0 | NA | |
106 | hsa-miR-590-3p | IGF1 | -0.28 | 0.59127 | 0.01 | 0.98747 | MirTarget; miRanda; mirMAP; miRNATAP | -0.9 | 0 | NA | |
107 | hsa-miR-592 | IGF1 | -0.18 | 0.85623 | 0.01 | 0.98747 | mirMAP | -0.18 | 0.00559 | NA | |
108 | hsa-miR-629-5p | IGF1 | -0.39 | 0.79854 | 0.01 | 0.98747 | mirMAP | -0.58 | 3.0E-5 | NA | |
109 | hsa-miR-940 | IGF1 | -0.23 | 0.68006 | 0.01 | 0.98747 | MirTarget; PITA; miRNATAP | -0.57 | 0 | NA | |
110 | hsa-miR-22-5p | PDPK1 | -0.08 | 0.9317 | -0 | 0.99893 | miRNATAP | -0.11 | 0.00108 | NA | |
111 | hsa-miR-429 | PGF | -0.46 | 0.80624 | 0.25 | 0.74206 | miRNATAP | -0.16 | 0.0028 | NA | |
112 | hsa-let-7f-1-3p | PIK3CA | -0.31 | 0.69341 | 0.02 | 0.97942 | mirMAP | -0.12 | 0.00648 | NA | |
113 | hsa-miR-148a-5p | PIK3CA | -0.45 | 0.74842 | 0.02 | 0.97942 | mirMAP | -0.11 | 7.0E-5 | NA | |
114 | hsa-miR-148b-3p | PIK3CA | -0.2 | 0.91188 | 0.02 | 0.97942 | miRNAWalker2 validate | -0.12 | 0.00491 | NA | |
115 | hsa-miR-16-2-3p | PIK3CA | -0.37 | 0.54685 | 0.02 | 0.97942 | mirMAP | -0.1 | 9.0E-5 | NA | |
116 | hsa-miR-17-5p | PIK3CA | -0.18 | 0.93454 | 0.02 | 0.97942 | miRNAWalker2 validate | -0.12 | 0 | NA | |
117 | hsa-miR-186-5p | PIK3CA | -0.32 | 0.85413 | 0.02 | 0.97942 | mirMAP | -0.15 | 0.00027 | NA | |
118 | hsa-miR-32-3p | PIK3CA | -0.57 | 0.13133 | 0.02 | 0.97942 | mirMAP | -0.11 | 0 | NA | |
119 | hsa-miR-335-5p | PIK3CA | -0.03 | 0.97338 | 0.02 | 0.97942 | miRNAWalker2 validate | -0.1 | 0.0001 | NA | |
120 | hsa-miR-339-5p | PIK3CA | -0.3 | 0.71291 | 0.02 | 0.97942 | miRanda | -0.1 | 1.0E-5 | NA | |
121 | hsa-miR-374b-5p | PIK3CA | -0.29 | 0.8357 | 0.02 | 0.97942 | mirMAP | -0.14 | 0.00032 | NA | |
122 | hsa-miR-501-5p | PIK3CA | -0.83 | 0.05827 | 0.02 | 0.97942 | mirMAP | -0.11 | 0 | NA | |
123 | hsa-miR-576-5p | PIK3CA | -0.51 | 0.41719 | 0.02 | 0.97942 | PITA | -0.11 | 7.0E-5 | NA | |
124 | hsa-miR-582-3p | PIK3CA | -0.23 | 0.89768 | 0.02 | 0.97942 | miRNATAP | -0.14 | 0 | NA | |
125 | hsa-miR-590-3p | PIK3CA | -0.28 | 0.59127 | 0.02 | 0.97942 | miRanda; mirMAP | -0.12 | 0 | NA | |
126 | hsa-miR-590-5p | PIK3CA | -0.55 | 0.47274 | 0.02 | 0.97942 | miRanda | -0.14 | 0 | NA | |
127 | hsa-miR-96-5p | PIK3CA | 0.09 | 0.92309 | 0.02 | 0.97942 | TargetScan | -0.13 | 0 | NA | |
128 | hsa-miR-1468-5p | PIK3CD | -0.2 | 0.68841 | -0.05 | 0.94703 | MirTarget | -0.29 | 0.00025 | NA | |
129 | hsa-miR-29a-3p | PIK3CD | 0.01 | 0.99698 | -0.05 | 0.94703 | mirMAP | -0.35 | 0.00244 | NA | |
130 | hsa-miR-29b-3p | PIK3CD | -0.1 | 0.95899 | -0.05 | 0.94703 | mirMAP | -0.26 | 0.00266 | NA | |
131 | hsa-miR-30b-5p | PIK3CD | -0.01 | 0.99462 | -0.05 | 0.94703 | MirTarget | -0.4 | 0 | NA | |
132 | hsa-miR-30c-5p | PIK3CD | -0.3 | 0.86581 | -0.05 | 0.94703 | MirTarget; miRNATAP | -0.42 | 0.00071 | NA | |
133 | hsa-miR-30d-5p | PIK3CD | -0.17 | 0.95173 | -0.05 | 0.94703 | MirTarget; miRNATAP | -0.36 | 0.00123 | NA | |
134 | hsa-miR-421 | PIK3CD | -0.18 | 0.7347 | -0.05 | 0.94703 | miRanda | -0.49 | 0 | NA | |
135 | hsa-miR-484 | PIK3CD | -0.18 | 0.88633 | -0.05 | 0.94703 | MirTarget; miRNATAP | -0.35 | 0.00143 | NA | |
136 | hsa-miR-7-5p | PIK3CD | 0.21 | 0.77371 | -0.05 | 0.94703 | miRTarBase; MirTarget; miRNATAP | -0.2 | 0.00035 | 22234835 | We first screened and identified a novel miR-7 target phosphoinositide 3-kinase catalytic subunit delta PIK3CD; A correlation between miR-7 and PIK3CD expression was also confirmed in clinical samples of HCC; By targeting PIK3CD mTOR and p70S6K miR-7 efficiently regulates the PI3K/Akt pathway |
137 | hsa-miR-942-5p | PIK3CD | -0.51 | 0.50778 | -0.05 | 0.94703 | MirTarget | -0.19 | 0.00863 | NA | |
138 | hsa-miR-126-3p | PIK3CG | -0.11 | 0.96367 | -0.36 | 0.46972 | miRTarBase | -0.53 | 0.00048 | NA | |
139 | hsa-miR-26b-5p | PIK3CG | -0.02 | 0.99038 | -0.36 | 0.46972 | miRNAWalker2 validate | -0.8 | 0 | NA | |
140 | hsa-miR-29b-3p | PIK3CG | -0.1 | 0.95899 | -0.36 | 0.46972 | miRTarBase | -0.67 | 0 | NA | |
141 | hsa-miR-335-3p | PIK3CG | -0.24 | 0.8845 | -0.36 | 0.46972 | mirMAP | -0.56 | 0 | NA | |
142 | hsa-miR-421 | PIK3CG | -0.18 | 0.7347 | -0.36 | 0.46972 | miRanda | -0.44 | 0.00013 | NA | |
143 | hsa-miR-502-5p | PIK3CG | -0.71 | 0.02613 | -0.36 | 0.46972 | miRNATAP | -0.34 | 0.00065 | 26163264 | Phosphoinositide 3-kinase catalytic subunit gamma PIK3CG was identified as a direct downstream target of miR-502 in HCC cells; Notably overexpression of PIK3CG reversed the inhibitory effects of miR-502 in HCC cells |
144 | hsa-miR-590-3p | PIK3CG | -0.28 | 0.59127 | -0.36 | 0.46972 | miRanda | -0.44 | 1.0E-5 | NA | |
145 | hsa-miR-132-3p | PIK3R1 | -0.24 | 0.87175 | -0.11 | 0.93752 | MirTarget | -0.19 | 0.0073 | NA | |
146 | hsa-miR-15a-5p | PIK3R1 | -0.07 | 0.96484 | -0.11 | 0.93752 | MirTarget | -0.22 | 9.0E-5 | NA | |
147 | hsa-miR-15b-5p | PIK3R1 | -0.27 | 0.87097 | -0.11 | 0.93752 | MirTarget | -0.14 | 0.00644 | NA | |
148 | hsa-miR-16-5p | PIK3R1 | 0.01 | 0.99448 | -0.11 | 0.93752 | MirTarget | -0.19 | 0.00026 | NA | |
149 | hsa-miR-185-5p | PIK3R1 | -0.29 | 0.82059 | -0.11 | 0.93752 | miRNATAP | -0.24 | 0.00027 | NA | |
150 | hsa-miR-21-5p | PIK3R1 | -0.15 | 0.97024 | -0.11 | 0.93752 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.32 | 4.0E-5 | 26676464 | PIK3R1 targeting by miR 21 suppresses tumor cell migration and invasion by reducing PI3K/AKT signaling and reversing EMT and predicts clinical outcome of breast cancer; Next we identified the PIK3R1 as a direct target of miR-21 and showed that it was negatively regulated by miR-21; Taken together we provide novel evidence that miR-21 knockdown suppresses cell growth migration and invasion partly by inhibiting PI3K/AKT activation via direct targeting PIK3R1 and reversing EMT in breast cancer |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | PHOSPHORYLATION | 21 | 1228 | 5.272e-18 | 2.453e-14 |
2 | PROTEIN PHOSPHORYLATION | 19 | 944 | 2.34e-17 | 5.445e-14 |
3 | INTRACELLULAR SIGNAL TRANSDUCTION | 22 | 1572 | 3.621e-17 | 5.616e-14 |
4 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 22 | 1977 | 4.584e-15 | 4.43e-12 |
5 | INOSITOL LIPID MEDIATED SIGNALING | 10 | 124 | 4.76e-15 | 4.43e-12 |
6 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 19 | 1618 | 4.382e-13 | 3.398e-10 |
7 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 20 | 1929 | 7.371e-13 | 4.9e-10 |
8 | PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 6 | 25 | 2.16e-12 | 1.256e-09 |
9 | REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 18 | 1656 | 9.497e-12 | 4.91e-09 |
10 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE SIGNALING PATHWAY | 12 | 498 | 1.099e-11 | 5.114e-09 |
11 | VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 7 | 74 | 2.808e-11 | 1.168e-08 |
12 | RESPONSE TO INSULIN | 9 | 205 | 3.265e-11 | 1.168e-08 |
13 | NEGATIVE REGULATION OF CELL DEATH | 14 | 872 | 3.058e-11 | 1.168e-08 |
14 | CELLULAR RESPONSE TO HORMONE STIMULUS | 12 | 552 | 3.631e-11 | 1.207e-08 |
15 | CELLULAR RESPONSE TO INSULIN STIMULUS | 8 | 146 | 7.91e-11 | 2.454e-08 |
16 | PEPTIDYL SERINE MODIFICATION | 8 | 148 | 8.823e-11 | 2.566e-08 |
17 | PHOSPHATIDYLINOSITOL 3 PHOSPHATE BIOSYNTHETIC PROCESS | 6 | 49 | 1.659e-10 | 4.541e-08 |
18 | REGULATION OF CELL DEATH | 16 | 1472 | 2.402e-10 | 6.21e-08 |
19 | POSITIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 14 | 1036 | 2.983e-10 | 6.939e-08 |
20 | POSITIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 14 | 1036 | 2.983e-10 | 6.939e-08 |
21 | ENZYME LINKED RECEPTOR PROTEIN SIGNALING PATHWAY | 12 | 689 | 4.641e-10 | 1.028e-07 |
22 | REGULATION OF GLUCOSE IMPORT | 6 | 60 | 5.864e-10 | 1.24e-07 |
23 | RESPONSE TO PEPTIDE | 10 | 404 | 6.191e-10 | 1.245e-07 |
24 | RESPONSE TO HORMONE | 13 | 893 | 6.421e-10 | 1.245e-07 |
25 | PHOSPHATIDYLINOSITOL BIOSYNTHETIC PROCESS | 7 | 120 | 8.806e-10 | 1.639e-07 |
26 | RESPONSE TO OXYGEN CONTAINING COMPOUND | 15 | 1381 | 1.137e-09 | 2.035e-07 |
27 | REGULATION OF TOR SIGNALING | 6 | 68 | 1.27e-09 | 2.189e-07 |
28 | CELLULAR RESPONSE TO OXYGEN CONTAINING COMPOUND | 12 | 799 | 2.492e-09 | 4.142e-07 |
29 | CELLULAR RESPONSE TO ENDOGENOUS STIMULUS | 13 | 1008 | 2.803e-09 | 4.497e-07 |
30 | REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 5 | 36 | 3.238e-09 | 5.022e-07 |
31 | POSITIVE REGULATION OF EPITHELIAL CELL PROLIFERATION | 7 | 154 | 5.054e-09 | 7.586e-07 |
32 | CELLULAR RESPONSE TO NITROGEN COMPOUND | 10 | 505 | 5.297e-09 | 7.702e-07 |
33 | RESPONSE TO NITROGEN COMPOUND | 12 | 859 | 5.628e-09 | 7.935e-07 |
34 | POSITIVE REGULATION OF IMMUNE SYSTEM PROCESS | 12 | 867 | 6.244e-09 | 8.545e-07 |
35 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 16 | 1848 | 6.723e-09 | 8.689e-07 |
36 | REGULATION OF GENERATION OF PRECURSOR METABOLITES AND ENERGY | 6 | 89 | 6.581e-09 | 8.689e-07 |
37 | REGULATION OF CELLULAR CARBOHYDRATE CATABOLIC PROCESS | 5 | 42 | 7.254e-09 | 8.883e-07 |
38 | REGULATION OF CARBOHYDRATE CATABOLIC PROCESS | 5 | 42 | 7.254e-09 | 8.883e-07 |
39 | CELLULAR RESPONSE TO PEPTIDE | 8 | 274 | 1.156e-08 | 1.38e-06 |
40 | LIPID PHOSPHORYLATION | 6 | 99 | 1.254e-08 | 1.459e-06 |
41 | REGULATION OF GLUCOSE TRANSPORT | 6 | 100 | 1.333e-08 | 1.513e-06 |
42 | REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 4 | 17 | 1.439e-08 | 1.558e-06 |
43 | POSITIVE REGULATION OF NUCLEOTIDE CATABOLIC PROCESS | 4 | 17 | 1.439e-08 | 1.558e-06 |
44 | REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 5 | 49 | 1.613e-08 | 1.668e-06 |
45 | REGULATION OF ATP METABOLIC PROCESS | 5 | 49 | 1.613e-08 | 1.668e-06 |
46 | REGULATION OF COENZYME METABOLIC PROCESS | 5 | 50 | 1.79e-08 | 1.772e-06 |
47 | REGULATION OF COFACTOR METABOLIC PROCESS | 5 | 50 | 1.79e-08 | 1.772e-06 |
48 | POSITIVE REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 8 | 296 | 2.109e-08 | 2.044e-06 |
49 | RESPONSE TO ENDOGENOUS STIMULUS | 14 | 1450 | 2.298e-08 | 2.182e-06 |
50 | PHOSPHATIDYLINOSITOL METABOLIC PROCESS | 7 | 193 | 2.414e-08 | 2.247e-06 |
51 | REGULATION OF KINASE ACTIVITY | 11 | 776 | 2.476e-08 | 2.259e-06 |
52 | REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 6 | 118 | 3.609e-08 | 3.229e-06 |
53 | RESPONSE TO ABIOTIC STIMULUS | 12 | 1024 | 3.974e-08 | 3.489e-06 |
54 | REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 5 | 59 | 4.185e-08 | 3.606e-06 |
55 | LIPID MODIFICATION | 7 | 210 | 4.314e-08 | 3.65e-06 |
56 | GLYCEROLIPID BIOSYNTHETIC PROCESS | 7 | 211 | 4.457e-08 | 3.703e-06 |
57 | CELL MOTILITY | 11 | 835 | 5.24e-08 | 4.204e-06 |
58 | LOCALIZATION OF CELL | 11 | 835 | 5.24e-08 | 4.204e-06 |
59 | CELLULAR RESPONSE TO STRESS | 14 | 1565 | 6.026e-08 | 4.753e-06 |
60 | POSITIVE REGULATION OF NUCLEOSIDE METABOLIC PROCESS | 4 | 24 | 6.374e-08 | 4.862e-06 |
61 | POSITIVE REGULATION OF ATP METABOLIC PROCESS | 4 | 24 | 6.374e-08 | 4.862e-06 |
62 | REGULATION OF CELLULAR AMIDE METABOLIC PROCESS | 8 | 354 | 8.4e-08 | 6.304e-06 |
63 | POSITIVE REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 5 | 68 | 8.624e-08 | 6.369e-06 |
64 | PHOSPHOLIPID BIOSYNTHETIC PROCESS | 7 | 235 | 9.314e-08 | 6.771e-06 |
65 | LOCOMOTION | 12 | 1114 | 1.002e-07 | 7.174e-06 |
66 | REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 4 | 27 | 1.049e-07 | 7.397e-06 |
67 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 12 | 1135 | 1.229e-07 | 8.533e-06 |
68 | POSITIVE REGULATION OF DEVELOPMENTAL PROCESS | 12 | 1142 | 1.314e-07 | 8.991e-06 |
69 | POSITIVE REGULATION OF CELL ADHESION | 8 | 376 | 1.334e-07 | 8.994e-06 |
70 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 14 | 1672 | 1.379e-07 | 9.166e-06 |
71 | LIPID BIOSYNTHETIC PROCESS | 9 | 539 | 1.52e-07 | 9.959e-06 |
72 | NEGATIVE REGULATION OF TOR SIGNALING | 4 | 30 | 1.633e-07 | 1.055e-05 |
73 | REGULATION OF PROTEIN MODIFICATION PROCESS | 14 | 1710 | 1.824e-07 | 1.162e-05 |
74 | REGULATION OF TRANSFERASE ACTIVITY | 11 | 946 | 1.856e-07 | 1.167e-05 |
75 | INSULIN RECEPTOR SIGNALING PATHWAY | 5 | 80 | 1.961e-07 | 1.217e-05 |
76 | REGULATION OF CELLULAR COMPONENT MOVEMENT | 10 | 771 | 2.828e-07 | 1.731e-05 |
77 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 13 | 1492 | 2.928e-07 | 1.77e-05 |
78 | POSITIVE REGULATION OF LOCOMOTION | 8 | 420 | 3.101e-07 | 1.839e-05 |
79 | GLUCOSE HOMEOSTASIS | 6 | 170 | 3.161e-07 | 1.839e-05 |
80 | CARBOHYDRATE HOMEOSTASIS | 6 | 170 | 3.161e-07 | 1.839e-05 |
81 | REGULATION OF LIPID METABOLIC PROCESS | 7 | 282 | 3.21e-07 | 1.844e-05 |
82 | REGULATION OF EPITHELIAL CELL PROLIFERATION | 7 | 285 | 3.448e-07 | 1.957e-05 |
83 | POSITIVE REGULATION OF CELL COMMUNICATION | 13 | 1532 | 3.975e-07 | 2.202e-05 |
84 | RESPONSE TO EXTERNAL STIMULUS | 14 | 1821 | 3.968e-07 | 2.202e-05 |
85 | ANGIOGENESIS | 7 | 293 | 4.156e-07 | 2.275e-05 |
86 | MOVEMENT OF CELL OR SUBCELLULAR COMPONENT | 12 | 1275 | 4.33e-07 | 2.343e-05 |
87 | GLYCEROPHOSPHOLIPID METABOLIC PROCESS | 7 | 297 | 4.553e-07 | 2.435e-05 |
88 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 4 | 40 | 5.382e-07 | 2.836e-05 |
89 | REGULATION OF ENDOTHELIAL CELL PROLIFERATION | 5 | 98 | 5.425e-07 | 2.836e-05 |
90 | REGULATION OF CELL ADHESION | 9 | 629 | 5.577e-07 | 2.883e-05 |
91 | RESPONSE TO OXYGEN LEVELS | 7 | 311 | 6.205e-07 | 3.173e-05 |
92 | POSITIVE REGULATION OF GLUCOSE TRANSPORT | 4 | 42 | 6.576e-07 | 3.326e-05 |
93 | POSITIVE REGULATION OF KINASE ACTIVITY | 8 | 482 | 8.776e-07 | 4.391e-05 |
94 | POSITIVE REGULATION OF GLUCOSE IMPORT IN RESPONSE TO INSULIN STIMULUS | 3 | 12 | 8.913e-07 | 4.412e-05 |
95 | REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 6 | 211 | 1.121e-06 | 5.492e-05 |
96 | REGULATION OF LIPID KINASE ACTIVITY | 4 | 48 | 1.135e-06 | 5.502e-05 |
97 | INDUCTION OF POSITIVE CHEMOTAXIS | 3 | 13 | 1.157e-06 | 5.552e-05 |
98 | REGULATION OF IMMUNE SYSTEM PROCESS | 12 | 1403 | 1.203e-06 | 5.711e-05 |
99 | GLYCEROLIPID METABOLIC PROCESS | 7 | 356 | 1.531e-06 | 7.195e-05 |
100 | REGULATED EXOCYTOSIS | 6 | 224 | 1.588e-06 | 7.388e-05 |
101 | PHOSPHOLIPID METABOLIC PROCESS | 7 | 364 | 1.774e-06 | 8.094e-05 |
102 | BLOOD VESSEL MORPHOGENESIS | 7 | 364 | 1.774e-06 | 8.094e-05 |
103 | REGULATION OF CELL CYCLE | 10 | 949 | 1.883e-06 | 8.507e-05 |
104 | REGULATION OF CATABOLIC PROCESS | 9 | 731 | 1.942e-06 | 8.69e-05 |
105 | TOR SIGNALING | 3 | 16 | 2.259e-06 | 9.914e-05 |
106 | POSITIVE REGULATION OF VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 3 | 16 | 2.259e-06 | 9.914e-05 |
107 | POSITIVE REGULATION OF CELL DIVISION | 5 | 132 | 2.375e-06 | 0.0001033 |
108 | POSITIVE REGULATION OF VASCULATURE DEVELOPMENT | 5 | 133 | 2.464e-06 | 0.0001062 |
109 | REGULATION OF TRANSPORT | 13 | 1804 | 2.556e-06 | 0.0001091 |
110 | RESPONSE TO WOUNDING | 8 | 563 | 2.798e-06 | 0.0001184 |
111 | REGULATION OF AUTOPHAGY | 6 | 249 | 2.93e-06 | 0.0001224 |
112 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 5 | 138 | 2.955e-06 | 0.0001224 |
113 | CELL ACTIVATION | 8 | 568 | 2.988e-06 | 0.0001224 |
114 | REGULATION OF PHOSPHOLIPID METABOLIC PROCESS | 4 | 61 | 2.999e-06 | 0.0001224 |
115 | REGULATION OF NEURON DEATH | 6 | 252 | 3.139e-06 | 0.000127 |
116 | PLATELET ACTIVATION | 5 | 142 | 3.4e-06 | 0.0001364 |
117 | LEUKOCYTE MIGRATION | 6 | 259 | 3.676e-06 | 0.0001462 |
118 | T CELL RECEPTOR SIGNALING PATHWAY | 5 | 146 | 3.896e-06 | 0.0001536 |
119 | REGULATION OF DNA TEMPLATED TRANSCRIPTION IN RESPONSE TO STRESS | 4 | 67 | 4.374e-06 | 0.000171 |
120 | POSITIVE REGULATION OF CELL PROLIFERATION | 9 | 814 | 4.687e-06 | 0.0001817 |
121 | REGULATION OF CELL DIVISION | 6 | 272 | 4.872e-06 | 0.0001873 |
122 | RESPONSE TO ACTIVITY | 4 | 69 | 4.922e-06 | 0.0001877 |
123 | CELL CYCLE ARREST | 5 | 154 | 5.058e-06 | 0.0001913 |
124 | POSITIVE REGULATION OF NEUROBLAST PROLIFERATION | 3 | 21 | 5.334e-06 | 0.0002002 |
125 | POSITIVE REGULATION OF TRANSFERASE ACTIVITY | 8 | 616 | 5.436e-06 | 0.0002008 |
126 | RESPONSE TO DRUG | 7 | 431 | 5.41e-06 | 0.0002008 |
127 | ACTIVATION OF PROTEIN KINASE ACTIVITY | 6 | 279 | 5.636e-06 | 0.0002065 |
128 | RESPONSE TO PURINE CONTAINING COMPOUND | 5 | 158 | 5.732e-06 | 0.0002084 |
129 | POSITIVE REGULATION OF PEPTIDYL TYROSINE PHOSPHORYLATION | 5 | 162 | 6.476e-06 | 0.0002336 |
130 | REGULATION OF GROWTH | 8 | 633 | 6.638e-06 | 0.0002376 |
131 | POSITIVE REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 4 | 75 | 6.872e-06 | 0.0002404 |
132 | CELLULAR GLUCOSE HOMEOSTASIS | 4 | 75 | 6.872e-06 | 0.0002404 |
133 | POSITIVE REGULATION OF AUTOPHAGY | 4 | 75 | 6.872e-06 | 0.0002404 |
134 | POSTTRANSCRIPTIONAL REGULATION OF GENE EXPRESSION | 7 | 448 | 6.967e-06 | 0.0002419 |
135 | POSITIVE REGULATION OF CELLULAR RESPONSE TO INSULIN STIMULUS | 3 | 23 | 7.087e-06 | 0.0002443 |
136 | ORGANOPHOSPHATE BIOSYNTHETIC PROCESS | 7 | 450 | 7.173e-06 | 0.0002454 |
137 | LYMPHOCYTE COSTIMULATION | 4 | 78 | 8.037e-06 | 0.0002728 |
138 | REGULATION OF POSITIVE CHEMOTAXIS | 3 | 24 | 8.09e-06 | 0.0002728 |
139 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 11 | 1395 | 8.441e-06 | 0.0002804 |
140 | POSITIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 9 | 876 | 8.496e-06 | 0.0002804 |
141 | NEGATIVE REGULATION OF NEURON DEATH | 5 | 171 | 8.425e-06 | 0.0002804 |
142 | REGULATION OF CARBOHYDRATE METABOLIC PROCESS | 5 | 172 | 8.667e-06 | 0.000284 |
143 | REGULATION OF MAPK CASCADE | 8 | 660 | 9.009e-06 | 0.0002931 |
144 | VASCULATURE DEVELOPMENT | 7 | 469 | 9.392e-06 | 0.0003014 |
145 | POSITIVE REGULATION OF PROTEIN KINASE B SIGNALING | 4 | 81 | 9.342e-06 | 0.0003014 |
146 | POSITIVE REGULATION OF MAPK CASCADE | 7 | 470 | 9.523e-06 | 0.0003014 |
147 | WOUND HEALING | 7 | 470 | 9.523e-06 | 0.0003014 |
148 | EXOCYTOSIS | 6 | 310 | 1.028e-05 | 0.0003234 |
149 | POSITIVE REGULATION OF CELL ACTIVATION | 6 | 311 | 1.048e-05 | 0.0003271 |
150 | POSITIVE REGULATION OF GENE EXPRESSION | 12 | 1733 | 1.088e-05 | 0.0003376 |
151 | CELLULAR LIPID METABOLIC PROCESS | 9 | 913 | 1.185e-05 | 0.0003652 |
152 | REGULATION OF NEUROBLAST PROLIFERATION | 3 | 28 | 1.304e-05 | 0.000399 |
153 | REGULATION OF RESPONSE TO EXTERNAL STIMULUS | 9 | 926 | 1.327e-05 | 0.0004037 |
154 | REGULATION OF RESPONSE TO STRESS | 11 | 1468 | 1.371e-05 | 0.0004143 |
155 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 12 | 1791 | 1.523e-05 | 0.0004571 |
156 | REGULATION OF BODY FLUID LEVELS | 7 | 506 | 1.536e-05 | 0.0004583 |
157 | ANTIGEN RECEPTOR MEDIATED SIGNALING PATHWAY | 5 | 195 | 1.591e-05 | 0.0004707 |
158 | REGULATION OF CELL DIFFERENTIATION | 11 | 1492 | 1.598e-05 | 0.0004707 |
159 | REGULATION OF CELL PROLIFERATION | 11 | 1496 | 1.639e-05 | 0.0004797 |
160 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 11 | 1518 | 1.881e-05 | 0.000547 |
161 | PROTEIN KINASE B SIGNALING | 3 | 34 | 2.365e-05 | 0.0006835 |
162 | REGULATION OF PEPTIDYL TYROSINE PHOSPHORYLATION | 5 | 213 | 2.433e-05 | 0.0006989 |
163 | CELL DEATH | 9 | 1001 | 2.468e-05 | 0.0007044 |
164 | CIRCULATORY SYSTEM PROCESS | 6 | 366 | 2.629e-05 | 0.000746 |
165 | PLATELET DEGRANULATION | 4 | 107 | 2.812e-05 | 0.0007892 |
166 | POSITIVE CHEMOTAXIS | 3 | 36 | 2.816e-05 | 0.0007892 |
167 | CARDIOVASCULAR SYSTEM DEVELOPMENT | 8 | 788 | 3.239e-05 | 0.000897 |
168 | CIRCULATORY SYSTEM DEVELOPMENT | 8 | 788 | 3.239e-05 | 0.000897 |
169 | CELL CYCLE | 10 | 1316 | 3.363e-05 | 0.0009259 |
170 | REGULATION OF CELLULAR RESPONSE TO GROWTH FACTOR STIMULUS | 5 | 229 | 3.442e-05 | 0.0009421 |
171 | REGULATION OF VASCULATURE DEVELOPMENT | 5 | 233 | 3.739e-05 | 0.001017 |
172 | AUTOPHAGY | 6 | 394 | 3.972e-05 | 0.001075 |
173 | SECRETION | 7 | 588 | 4.023e-05 | 0.001082 |
174 | POSITIVE REGULATION OF GROWTH | 5 | 238 | 4.137e-05 | 0.001106 |
175 | IMMUNE SYSTEM PROCESS | 12 | 1984 | 4.263e-05 | 0.001134 |
176 | POSITIVE REGULATION OF CELL DIFFERENTIATION | 8 | 823 | 4.413e-05 | 0.001167 |
177 | POSITIVE REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 3 | 42 | 4.497e-05 | 0.001182 |
178 | POSITIVE REGULATION OF CELL CELL ADHESION | 5 | 243 | 4.567e-05 | 0.001187 |
179 | REGULATION OF PROTEIN KINASE B SIGNALING | 4 | 121 | 4.554e-05 | 0.001187 |
180 | RESPONSE TO ELECTRICAL STIMULUS | 3 | 43 | 4.828e-05 | 0.001248 |
181 | POSITIVE REGULATION OF MITOTIC CELL CYCLE | 4 | 123 | 4.855e-05 | 0.001248 |
182 | REGULATION OF CELL DEVELOPMENT | 8 | 836 | 4.931e-05 | 0.001261 |
183 | PEPTIDYL AMINO ACID MODIFICATION | 8 | 841 | 5.144e-05 | 0.001308 |
184 | ACTIVATION OF IMMUNE RESPONSE | 6 | 427 | 6.211e-05 | 0.001571 |
185 | POSITIVE REGULATION OF PURINE NUCLEOTIDE METABOLIC PROCESS | 4 | 133 | 6.585e-05 | 0.001647 |
186 | POSITIVE REGULATION OF NUCLEOTIDE METABOLIC PROCESS | 4 | 133 | 6.585e-05 | 0.001647 |
187 | CHEMICAL HOMEOSTASIS | 8 | 874 | 6.749e-05 | 0.001653 |
188 | POSITIVE REGULATION OF RESPONSE TO EXTRACELLULAR STIMULUS | 3 | 48 | 6.729e-05 | 0.001653 |
189 | NEGATIVE REGULATION OF CELL CYCLE | 6 | 433 | 6.71e-05 | 0.001653 |
190 | POSITIVE REGULATION OF RESPONSE TO NUTRIENT LEVELS | 3 | 48 | 6.729e-05 | 0.001653 |
191 | NEGATIVE REGULATION OF NEURON APOPTOTIC PROCESS | 4 | 135 | 6.979e-05 | 0.0017 |
192 | RESPONSE TO EXTRACELLULAR STIMULUS | 6 | 441 | 7.424e-05 | 0.001799 |
193 | LIPID METABOLIC PROCESS | 9 | 1158 | 7.718e-05 | 0.001861 |
194 | FC EPSILON RECEPTOR SIGNALING PATHWAY | 4 | 142 | 8.493e-05 | 0.002037 |
195 | CELLULAR RESPONSE TO OXYGEN LEVELS | 4 | 143 | 8.727e-05 | 0.002082 |
196 | MACROAUTOPHAGY | 5 | 281 | 9.085e-05 | 0.002157 |
197 | NEGATIVE REGULATION OF CELL COMMUNICATION | 9 | 1192 | 9.647e-05 | 0.002279 |
198 | POSITIVE REGULATION OF CELL GROWTH | 4 | 148 | 9.97e-05 | 0.002343 |
199 | EPIDERMAL GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 3 | 55 | 0.0001013 | 0.002368 |
200 | REGULATION OF DEVELOPMENTAL GROWTH | 5 | 289 | 0.0001037 | 0.0024 |
201 | POSITIVE REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 5 | 289 | 0.0001037 | 0.0024 |
202 | REGULATION OF PROTEIN SERINE THREONINE KINASE ACTIVITY | 6 | 470 | 0.0001054 | 0.002428 |
203 | POSITIVE REGULATION OF TRANSPORT | 8 | 936 | 0.000109 | 0.002499 |
204 | RESPONSE TO STARVATION | 4 | 154 | 0.0001163 | 0.002652 |
205 | REGULATION OF CELL ACTIVATION | 6 | 484 | 0.0001238 | 0.002809 |
206 | SECRETION BY CELL | 6 | 486 | 0.0001266 | 0.002845 |
207 | IMMUNE EFFECTOR PROCESS | 6 | 486 | 0.0001266 | 0.002845 |
208 | VESICLE MEDIATED TRANSPORT | 9 | 1239 | 0.0001297 | 0.002902 |
209 | POSITIVE REGULATION OF SMOOTH MUSCLE CELL PROLIFERATION | 3 | 60 | 0.0001314 | 0.002924 |
210 | REGULATION OF HOMOTYPIC CELL CELL ADHESION | 5 | 307 | 0.0001376 | 0.003043 |
211 | POSITIVE REGULATION OF STEM CELL PROLIFERATION | 3 | 61 | 0.000138 | 0.003043 |
212 | POSITIVE REGULATION OF VASCULAR PERMEABILITY | 2 | 11 | 0.0001439 | 0.003158 |
213 | HEMOSTASIS | 5 | 311 | 0.0001462 | 0.003193 |
214 | RESPONSE TO OSMOTIC STRESS | 3 | 63 | 0.0001519 | 0.003303 |
215 | REGULATION OF EPITHELIAL CELL MIGRATION | 4 | 166 | 0.0001552 | 0.003359 |
216 | RESPONSE TO CARBOHYDRATE | 4 | 168 | 0.0001625 | 0.003501 |
217 | REGULATION OF MAP KINASE ACTIVITY | 5 | 319 | 0.0001645 | 0.003528 |
218 | FATTY ACID HOMEOSTASIS | 2 | 12 | 0.0001725 | 0.003664 |
219 | POSITIVE REGULATION OF ESTABLISHMENT OF PROTEIN LOCALIZATION | 6 | 514 | 0.0001717 | 0.003664 |
220 | IMMUNE RESPONSE REGULATING CELL SURFACE RECEPTOR SIGNALING PATHWAY | 5 | 323 | 0.0001744 | 0.003688 |
221 | REGULATION OF CELL SUBSTRATE ADHESION | 4 | 173 | 0.0001819 | 0.003824 |
222 | CELLULAR RESPONSE TO DRUG | 3 | 67 | 0.0001824 | 0.003824 |
223 | REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 7 | 750 | 0.0001846 | 0.003852 |
224 | REGULATION OF CELLULAR COMPONENT BIOGENESIS | 7 | 767 | 0.0002119 | 0.004402 |
225 | SINGLE ORGANISM BIOSYNTHETIC PROCESS | 9 | 1340 | 0.0002349 | 0.0048 |
226 | CELLULAR RESPONSE TO ELECTRICAL STIMULUS | 2 | 14 | 0.0002373 | 0.0048 |
227 | REGULATION OF FIBROBLAST APOPTOTIC PROCESS | 2 | 14 | 0.0002373 | 0.0048 |
228 | INSULIN LIKE GROWTH FACTOR RECEPTOR SIGNALING PATHWAY | 2 | 14 | 0.0002373 | 0.0048 |
229 | T CELL MIGRATION | 2 | 14 | 0.0002373 | 0.0048 |
230 | REGULATION OF NEURAL PRECURSOR CELL PROLIFERATION | 3 | 73 | 0.0002353 | 0.0048 |
231 | CELLULAR RESPONSE TO CARBOHYDRATE STIMULUS | 3 | 74 | 0.0002449 | 0.004934 |
232 | GRANULOCYTE MIGRATION | 3 | 75 | 0.0002549 | 0.005112 |
233 | REGULATION OF NEURON APOPTOTIC PROCESS | 4 | 192 | 0.0002709 | 0.00541 |
234 | RESPIRATORY BURST | 2 | 15 | 0.0002735 | 0.005439 |
235 | DEVELOPMENTAL MATURATION | 4 | 193 | 0.0002763 | 0.005471 |
236 | POSITIVE REGULATION OF IMMUNE RESPONSE | 6 | 563 | 0.0002808 | 0.005536 |
237 | POSITIVE REGULATION OF CELLULAR PROTEIN LOCALIZATION | 5 | 360 | 0.0002881 | 0.005656 |
238 | CELL CYCLE PROCESS | 8 | 1081 | 0.0002935 | 0.005737 |
239 | RESPONSE TO ALCOHOL | 5 | 362 | 0.0002956 | 0.005754 |
240 | ERBB SIGNALING PATHWAY | 3 | 79 | 0.0002971 | 0.005761 |
241 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 8 | 1087 | 0.0003047 | 0.005882 |
242 | POSITIVE REGULATION OF LEUKOCYTE CHEMOTAXIS | 3 | 81 | 0.0003199 | 0.00615 |
243 | NEUROGENESIS | 9 | 1402 | 0.0003294 | 0.006307 |
244 | REGULATION OF TRANSLATIONAL INITIATION | 3 | 82 | 0.0003316 | 0.006324 |
245 | REGULATION OF ENERGY HOMEOSTASIS | 2 | 17 | 0.0003535 | 0.006641 |
246 | FC RECEPTOR SIGNALING PATHWAY | 4 | 206 | 0.0003539 | 0.006641 |
247 | MAMMARY GLAND ALVEOLUS DEVELOPMENT | 2 | 17 | 0.0003535 | 0.006641 |
248 | MAMMARY GLAND LOBULE DEVELOPMENT | 2 | 17 | 0.0003535 | 0.006641 |
249 | POSITIVE REGULATION OF MAP KINASE ACTIVITY | 4 | 207 | 0.0003605 | 0.006737 |
250 | REGULATION OF CELL CELL ADHESION | 5 | 380 | 0.0003693 | 0.006847 |
251 | HEART PROCESS | 3 | 85 | 0.0003686 | 0.006847 |
252 | SINGLE ORGANISM BEHAVIOR | 5 | 384 | 0.0003875 | 0.007155 |
253 | CELLULAR RESPONSE TO PROSTAGLANDIN E STIMULUS | 2 | 18 | 0.0003973 | 0.00725 |
254 | RESPONSE TO CAFFEINE | 2 | 18 | 0.0003973 | 0.00725 |
255 | MAST CELL MEDIATED IMMUNITY | 2 | 18 | 0.0003973 | 0.00725 |
256 | NEGATIVE REGULATION OF CYSTEINE TYPE ENDOPEPTIDASE ACTIVITY | 3 | 88 | 0.0004082 | 0.007362 |
257 | REGULATION OF STEM CELL PROLIFERATION | 3 | 88 | 0.0004082 | 0.007362 |
258 | POSITIVE REGULATION OF PEPTIDYL SERINE PHOSPHORYLATION | 3 | 88 | 0.0004082 | 0.007362 |
259 | REGULATION OF CELL GROWTH | 5 | 391 | 0.0004208 | 0.007561 |
260 | REGULATION OF CELL MATRIX ADHESION | 3 | 90 | 0.000436 | 0.007803 |
261 | POSITIVE REGULATION OF CATABOLIC PROCESS | 5 | 395 | 0.0004409 | 0.00783 |
262 | GLAND DEVELOPMENT | 5 | 395 | 0.0004409 | 0.00783 |
263 | REGULATION OF TRANSLATION IN RESPONSE TO STRESS | 2 | 19 | 0.0004436 | 0.007848 |
264 | EMBRYONIC HEMOPOIESIS | 2 | 20 | 0.0004924 | 0.008645 |
265 | RESPONSE TO MUSCLE ACTIVITY | 2 | 20 | 0.0004924 | 0.008645 |
266 | ORGANOPHOSPHATE METABOLIC PROCESS | 7 | 885 | 0.0005049 | 0.008833 |
267 | FC GAMMA RECEPTOR SIGNALING PATHWAY | 3 | 95 | 0.0005108 | 0.008902 |
268 | REGULATION OF LEUKOCYTE CHEMOTAXIS | 3 | 96 | 0.0005267 | 0.009145 |
269 | MAST CELL ACTIVATION | 2 | 21 | 0.0005437 | 0.009369 |
270 | NEGATIVE REGULATION OF LIPID CATABOLIC PROCESS | 2 | 21 | 0.0005437 | 0.009369 |
271 | MYELOID LEUKOCYTE MIGRATION | 3 | 99 | 0.0005763 | 0.009822 |
272 | STRIATED MUSCLE CONTRACTION | 3 | 99 | 0.0005763 | 0.009822 |
273 | POSITIVE REGULATION OF CELL SUBSTRATE ADHESION | 3 | 99 | 0.0005763 | 0.009822 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | KINASE ACTIVITY | 20 | 842 | 8.388e-20 | 7.793e-17 |
2 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 20 | 992 | 2.092e-18 | 9.718e-16 |
3 | PROTEIN SERINE THREONINE KINASE ACTIVITY | 15 | 445 | 9.23e-17 | 2.858e-14 |
4 | PROTEIN KINASE ACTIVITY | 15 | 640 | 1.955e-14 | 4.54e-12 |
5 | PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 7 | 70 | 1.879e-11 | 3.491e-09 |
6 | X1 PHOSPHATIDYLINOSITOL 3 KINASE ACTIVITY | 6 | 43 | 7.283e-11 | 1.128e-08 |
7 | PHOSPHATIDYLINOSITOL KINASE ACTIVITY | 6 | 51 | 2.132e-10 | 2.829e-08 |
8 | ADENYL NUCLEOTIDE BINDING | 15 | 1514 | 4.034e-09 | 4.684e-07 |
9 | RIBONUCLEOTIDE BINDING | 16 | 1860 | 7.382e-09 | 7.62e-07 |
10 | KINASE BINDING | 10 | 606 | 2.989e-08 | 2.777e-06 |
11 | ENZYME BINDING | 14 | 1737 | 2.215e-07 | 1.87e-05 |
12 | PROTEIN SERINE THREONINE TYROSINE KINASE ACTIVITY | 4 | 39 | 4.849e-07 | 3.754e-05 |
13 | KINASE REGULATOR ACTIVITY | 6 | 186 | 5.364e-07 | 3.834e-05 |
14 | ENZYME REGULATOR ACTIVITY | 10 | 959 | 2.07e-06 | 0.0001373 |
15 | PHOSPHATIDYLINOSITOL PHOSPHATE KINASE ACTIVITY | 3 | 16 | 2.259e-06 | 0.0001399 |
16 | GROWTH FACTOR ACTIVITY | 5 | 160 | 6.095e-06 | 0.0003442 |
17 | MOLECULAR FUNCTION REGULATOR | 11 | 1353 | 6.298e-06 | 0.0003442 |
18 | PROTEIN HETERODIMERIZATION ACTIVITY | 7 | 468 | 9.262e-06 | 0.000478 |
19 | CHEMOATTRACTANT ACTIVITY | 3 | 27 | 1.165e-05 | 0.0005697 |
20 | INSULIN RECEPTOR BINDING | 3 | 32 | 1.965e-05 | 0.0009126 |
21 | PROTEIN PHOSPHATASE BINDING | 4 | 120 | 4.408e-05 | 0.00195 |
22 | MACROMOLECULAR COMPLEX BINDING | 10 | 1399 | 5.67e-05 | 0.002394 |
23 | RECEPTOR BINDING | 10 | 1476 | 8.916e-05 | 0.003601 |
24 | PHOSPHATASE BINDING | 4 | 162 | 0.0001413 | 0.005346 |
25 | INSULIN RECEPTOR SUBSTRATE BINDING | 2 | 11 | 0.0001439 | 0.005346 |
26 | INSULIN LIKE GROWTH FACTOR RECEPTOR BINDING | 2 | 15 | 0.0002735 | 0.009773 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | PHOSPHATIDYLINOSITOL 3 KINASE COMPLEX | 7 | 20 | 1.286e-15 | 7.511e-13 |
2 | TRANSFERASE COMPLEX TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 11 | 237 | 7.889e-14 | 2.304e-11 |
3 | EXTRINSIC COMPONENT OF MEMBRANE | 8 | 252 | 6.012e-09 | 1.17e-06 |
4 | TRANSFERASE COMPLEX | 11 | 703 | 8.943e-09 | 1.306e-06 |
5 | CATALYTIC COMPLEX | 11 | 1038 | 4.703e-07 | 5.493e-05 |
6 | PLATELET ALPHA GRANULE LUMEN | 4 | 55 | 1.974e-06 | 0.0001921 |
7 | PLATELET ALPHA GRANULE | 4 | 75 | 6.872e-06 | 0.0005734 |
8 | SECRETORY GRANULE LUMEN | 4 | 85 | 1.132e-05 | 0.0008261 |
9 | PROTEIN KINASE COMPLEX | 4 | 90 | 1.42e-05 | 0.0009213 |
10 | VESICLE LUMEN | 4 | 106 | 2.71e-05 | 0.001582 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | hsa04150_mTOR_signaling_pathway | 33 | 52 | 7.926e-92 | 1.427e-89 | |
2 | hsa04151_PI3K_AKT_signaling_pathway | 22 | 351 | 1.987e-31 | 1.788e-29 | |
3 | hsa04910_Insulin_signaling_pathway | 16 | 138 | 1.138e-26 | 6.826e-25 | |
4 | hsa04914_Progesterone.mediated_oocyte_maturation | 14 | 87 | 2.218e-25 | 9.983e-24 | |
5 | hsa04510_Focal_adhesion | 15 | 200 | 5.203e-22 | 1.873e-20 | |
6 | hsa04722_Neurotrophin_signaling_pathway | 13 | 127 | 7.481e-21 | 2.244e-19 | |
7 | hsa04012_ErbB_signaling_pathway | 11 | 87 | 9.81e-19 | 2.523e-17 | |
8 | hsa04960_Aldosterone.regulated_sodium_reabsorption | 9 | 42 | 1.178e-17 | 2.651e-16 | |
9 | hsa04370_VEGF_signaling_pathway | 9 | 76 | 3.628e-15 | 6.712e-14 | |
10 | hsa04973_Carbohydrate_digestion_and_absorption | 8 | 44 | 3.729e-15 | 6.712e-14 | |
11 | hsa04666_Fc_gamma_R.mediated_phagocytosis | 9 | 95 | 2.932e-14 | 4.797e-13 | |
12 | hsa04014_Ras_signaling_pathway | 11 | 236 | 7.531e-14 | 1.13e-12 | |
13 | hsa04662_B_cell_receptor_signaling_pathway | 8 | 75 | 3.429e-13 | 4.748e-12 | |
14 | hsa04664_Fc_epsilon_RI_signaling_pathway | 8 | 79 | 5.279e-13 | 6.787e-12 | |
15 | hsa04210_Apoptosis | 8 | 89 | 1.413e-12 | 1.696e-11 | |
16 | hsa04620_Toll.like_receptor_signaling_pathway | 8 | 102 | 4.325e-12 | 4.865e-11 | |
17 | hsa04660_T_cell_receptor_signaling_pathway | 8 | 108 | 6.896e-12 | 7.302e-11 | |
18 | hsa04062_Chemokine_signaling_pathway | 9 | 189 | 1.574e-11 | 1.574e-10 | |
19 | hsa04380_Osteoclast_differentiation | 8 | 128 | 2.739e-11 | 2.595e-10 | |
20 | hsa04070_Phosphatidylinositol_signaling_system | 7 | 78 | 4.103e-11 | 3.693e-10 | |
21 | hsa04650_Natural_killer_cell_mediated_cytotoxicity | 8 | 136 | 4.468e-11 | 3.83e-10 | |
22 | hsa04630_Jak.STAT_signaling_pathway | 8 | 155 | 1.278e-10 | 1.046e-09 | |
23 | hsa04670_Leukocyte_transendothelial_migration | 7 | 117 | 7.367e-10 | 5.765e-09 | |
24 | hsa04810_Regulation_of_actin_cytoskeleton | 8 | 214 | 1.663e-09 | 1.247e-08 | |
25 | hsa04720_Long.term_potentiation | 5 | 70 | 9.989e-08 | 7.192e-07 | |
26 | hsa04140_Regulation_of_autophagy | 4 | 34 | 2.75e-07 | 1.904e-06 | |
27 | hsa04114_Oocyte_meiosis | 5 | 114 | 1.151e-06 | 7.673e-06 | |
28 | hsa04010_MAPK_signaling_pathway | 6 | 268 | 4.474e-06 | 2.876e-05 | |
29 | hsa00562_Inositol_phosphate_metabolism | 3 | 57 | 0.0001127 | 0.0006995 | |
30 | hsa04920_Adipocytokine_signaling_pathway | 3 | 68 | 0.0001906 | 0.001144 | |
31 | hsa03013_RNA_transport | 3 | 152 | 0.001987 | 0.01154 | |
32 | hsa04730_Long.term_depression | 2 | 70 | 0.005944 | 0.03344 |
Num | lncRNA | miRNAs | miRNAs count | Gene | Sponge regulatory network | lncRNA log2FC | lncRNA pvalue | Gene log2FC | Gene pvalue | lncRNA-gene Pearson correlation |
---|---|---|---|---|---|---|---|---|---|---|
1 | EMX2OS |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-148a-5p;hsa-miR-15b-3p;hsa-miR-16-1-3p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-224-3p;hsa-miR-26b-5p;hsa-miR-27a-3p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-301a-3p;hsa-miR-32-3p;hsa-miR-33a-3p;hsa-miR-374b-3p;hsa-miR-421;hsa-miR-452-5p;hsa-miR-454-3p;hsa-miR-576-5p;hsa-miR-577;hsa-miR-590-3p;hsa-miR-592;hsa-miR-629-5p;hsa-miR-940 | 29 | IGF1 | Sponge network | 1.057 | 0.31716 | 0.009 | 0.98747 | 0.587 |
2 | EMX2OS |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-32-3p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-362-3p;hsa-miR-374b-5p;hsa-miR-421;hsa-miR-424-5p;hsa-miR-501-3p;hsa-miR-502-3p;hsa-miR-502-5p;hsa-miR-505-3p;hsa-miR-577;hsa-miR-663b;hsa-miR-93-5p | 25 | AKT3 | Sponge network | 1.057 | 0.31716 | 0.457 | 0.53933 | 0.542 |
3 | CECR7 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-1275;hsa-miR-130b-3p;hsa-miR-148a-5p;hsa-miR-15b-3p;hsa-miR-16-1-3p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-1-5p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-26b-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-301a-3p;hsa-miR-32-3p;hsa-miR-33a-3p;hsa-miR-361-5p;hsa-miR-362-5p;hsa-miR-454-3p;hsa-miR-590-3p;hsa-miR-592;hsa-miR-629-5p | 24 | IGF1 | Sponge network | 0.551 | 0.56177 | 0.009 | 0.98747 | 0.513 |
4 | CECR7 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-1275;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-32-3p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-362-3p;hsa-miR-362-5p;hsa-miR-501-3p;hsa-miR-502-3p;hsa-miR-502-5p;hsa-miR-93-5p | 20 | AKT3 | Sponge network | 0.551 | 0.56177 | 0.457 | 0.53933 | 0.508 |
5 | MEG3 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-15a-5p;hsa-miR-15b-5p;hsa-miR-16-5p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-335-3p;hsa-miR-577;hsa-miR-93-5p | 12 | AKT3 | Sponge network | 0.433 | 0.33816 | 0.457 | 0.53933 | 0.405 |
6 | MEG3 |
hsa-miR-130b-3p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-20a-3p;hsa-miR-26b-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-374b-3p;hsa-miR-576-5p;hsa-miR-577 | 10 | IGF1 | Sponge network | 0.433 | 0.33816 | 0.009 | 0.98747 | 0.37 |
7 | CECR7 |
hsa-let-7f-1-3p;hsa-miR-148a-5p;hsa-miR-148b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-32-3p;hsa-miR-335-5p;hsa-miR-582-3p;hsa-miR-590-3p;hsa-miR-590-5p | 11 | PIK3CA | Sponge network | 0.551 | 0.56177 | 0.023 | 0.97942 | 0.368 |
8 | CECR7 |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-let-7g-5p;hsa-miR-106b-5p;hsa-miR-10a-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-19a-3p;hsa-miR-200a-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-26a-1-3p;hsa-miR-26a-2-3p;hsa-miR-26b-5p;hsa-miR-32-3p;hsa-miR-331-3p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-429;hsa-miR-582-5p;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-93-5p | 30 | PRKAA2 | Sponge network | 0.551 | 0.56177 | 1.352 | 0.06117 | 0.309 |
9 | ZNF883 |
hsa-miR-106a-5p;hsa-miR-106b-5p;hsa-miR-107;hsa-miR-17-3p;hsa-miR-17-5p;hsa-miR-20a-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-335-3p;hsa-miR-33a-3p | 10 | AKT3 | Sponge network | 0.913 | 0.16772 | 0.457 | 0.53933 | 0.3 |
10 | EMX2OS |
hsa-let-7d-5p;hsa-let-7f-1-3p;hsa-let-7g-5p;hsa-miR-106b-5p;hsa-miR-10a-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-146a-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-182-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-19a-3p;hsa-miR-200a-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-21-3p;hsa-miR-26a-1-3p;hsa-miR-26a-2-3p;hsa-miR-26b-5p;hsa-miR-32-3p;hsa-miR-331-3p;hsa-miR-335-3p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-577;hsa-miR-590-3p;hsa-miR-7-1-3p;hsa-miR-93-5p | 32 | PRKAA2 | Sponge network | 1.057 | 0.31716 | 1.352 | 0.06117 | 0.292 |
11 | EMX2OS |
hsa-miR-130b-5p;hsa-miR-17-5p;hsa-miR-192-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-21-3p;hsa-miR-26b-5p;hsa-miR-335-5p;hsa-miR-378a-3p;hsa-miR-532-3p;hsa-miR-592;hsa-miR-760;hsa-miR-93-3p | 15 | RPS6KA2 | Sponge network | 1.057 | 0.31716 | 0.145 | 0.89703 | 0.27 |
12 | ZNF883 |
hsa-let-7a-3p;hsa-let-7f-1-3p;hsa-miR-130b-3p;hsa-miR-148a-5p;hsa-miR-15b-3p;hsa-miR-186-5p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-20a-3p;hsa-miR-26b-5p;hsa-miR-29a-3p;hsa-miR-29b-3p;hsa-miR-301a-3p;hsa-miR-33a-3p;hsa-miR-576-5p | 15 | IGF1 | Sponge network | 0.913 | 0.16772 | 0.009 | 0.98747 | 0.269 |
13 | HCG11 | hsa-let-7d-5p;hsa-let-7g-5p;hsa-miR-10a-5p;hsa-miR-130b-3p;hsa-miR-141-3p;hsa-miR-146a-5p;hsa-miR-15b-3p;hsa-miR-16-2-3p;hsa-miR-186-5p;hsa-miR-21-3p;hsa-miR-26a-1-3p;hsa-miR-33a-3p;hsa-miR-576-5p;hsa-miR-590-3p;hsa-miR-7-1-3p | 15 | PRKAA2 | Sponge network | 0.419 | 0.63279 | 1.352 | 0.06117 | 0.258 |
14 | CECR7 |
hsa-miR-130b-5p;hsa-miR-17-5p;hsa-miR-192-3p;hsa-miR-19a-3p;hsa-miR-19b-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-26b-5p;hsa-miR-335-5p;hsa-miR-378a-3p;hsa-miR-429;hsa-miR-532-3p;hsa-miR-592;hsa-miR-760 | 14 | RPS6KA2 | Sponge network | 0.551 | 0.56177 | 0.145 | 0.89703 | 0.258 |
15 | EMX2OS |
hsa-let-7f-1-3p;hsa-miR-148a-5p;hsa-miR-148b-3p;hsa-miR-16-2-3p;hsa-miR-17-5p;hsa-miR-186-5p;hsa-miR-32-3p;hsa-miR-335-5p;hsa-miR-339-5p;hsa-miR-374b-5p;hsa-miR-576-5p;hsa-miR-582-3p;hsa-miR-590-3p | 13 | PIK3CA | Sponge network | 1.057 | 0.31716 | 0.023 | 0.97942 | 0.254 |
16 | DGCR5 | hsa-let-7f-1-3p;hsa-miR-141-3p;hsa-miR-146a-5p;hsa-miR-186-5p;hsa-miR-192-5p;hsa-miR-200a-3p;hsa-miR-200b-3p;hsa-miR-200c-3p;hsa-miR-20a-5p;hsa-miR-30e-3p;hsa-miR-33a-3p;hsa-miR-576-5p | 12 | PRKAA2 | Sponge network | 0.256 | 0.70355 | 1.352 | 0.06117 | 0.251 |