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-140-5p | ABCC9 | 0.84 | 4.0E-5 | -2.76 | 0 | miRanda | -0.19 | 0.04837 | NA | |
2 | hsa-miR-152-3p | ABCD3 | -0.05 | 0.84435 | 0.14 | 0.52609 | MirTarget | -0.18 | 9.0E-5 | NA | |
3 | hsa-miR-140-5p | ABLIM1 | 0.84 | 4.0E-5 | -1.72 | 0 | PITA; miRanda | -0.24 | 0.00036 | NA | |
4 | hsa-miR-140-5p | ACACA | 0.84 | 4.0E-5 | -0.16 | 0.29248 | miRanda | -0.17 | 0 | NA | |
5 | hsa-miR-34a-5p | ACSL4 | 1.9 | 0 | -0.41 | 0.0792 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.13 | 0.00399 | NA | |
6 | hsa-miR-194-5p | ACTR3 | 1.9 | 0 | -0.05 | 0.71644 | mirMAP | -0.11 | 0 | NA | |
7 | hsa-miR-140-5p | ADAM10 | 0.84 | 4.0E-5 | 0.67 | 0.00766 | MirTarget; PITA; miRanda | -0.12 | 0.04176 | NA | |
8 | hsa-miR-34a-5p | ADAM22 | 1.9 | 0 | -1.12 | 0.02589 | MirTarget; miRNATAP | -0.32 | 0.00075 | NA | |
9 | hsa-miR-140-5p | ADAM9 | 0.84 | 4.0E-5 | -0.2 | 0.40665 | PITA; miRanda; miRNATAP | -0.21 | 0.00023 | NA | |
10 | hsa-miR-152-3p | ADAMTS19 | -0.05 | 0.84435 | -2.99 | 0 | MirTarget | -0.65 | 0 | NA | |
11 | hsa-miR-34a-5p | ADAMTS2 | 1.9 | 0 | -0.77 | 0.15763 | MirTarget | -0.53 | 0 | NA | |
12 | hsa-miR-194-5p | ADAMTS5 | 1.9 | 0 | -2.16 | 0 | mirMAP | -0.26 | 0 | NA | |
13 | hsa-miR-34a-5p | ADARB1 | 1.9 | 0 | -1.93 | 0 | miRNAWalker2 validate | -0.48 | 0 | NA | |
14 | hsa-miR-34a-5p | AFAP1L2 | 1.9 | 0 | 0.06 | 0.85809 | miRNAWalker2 validate | -0.18 | 0.00406 | NA | |
15 | hsa-miR-34a-5p | AFF4 | 1.9 | 0 | -0.82 | 0 | miRNATAP | -0.11 | 0.00024 | NA | |
16 | hsa-miR-140-5p | AGAP1 | 0.84 | 4.0E-5 | -0.4 | 0.01021 | miRanda | -0.12 | 0.00085 | NA | |
17 | hsa-miR-34a-5p | AHNAK | 1.9 | 0 | -1.66 | 0 | miRNAWalker2 validate | -0.3 | 0 | NA | |
18 | hsa-miR-140-5p | AKAP11 | 0.84 | 4.0E-5 | -0.8 | 0 | MirTarget; miRanda | -0.18 | 1.0E-5 | NA | |
19 | hsa-miR-140-5p | AKAP13 | 0.84 | 4.0E-5 | -1.15 | 0 | miRanda | -0.16 | 1.0E-5 | NA | |
20 | hsa-miR-34a-5p | AKAP13 | 1.9 | 0 | -1.15 | 0 | mirMAP | -0.21 | 0 | NA | |
21 | hsa-miR-140-5p | AKAP6 | 0.84 | 4.0E-5 | -3.34 | 0 | miRanda | -0.44 | 3.0E-5 | NA | |
22 | hsa-miR-34a-5p | AKAP6 | 1.9 | 0 | -3.34 | 0 | MirTarget | -0.91 | 0 | NA | |
23 | hsa-miR-152-3p | AKAP7 | -0.05 | 0.84435 | -1.26 | 1.0E-5 | MirTarget | -0.18 | 0.00129 | NA | |
24 | hsa-miR-34a-5p | ALCAM | 1.9 | 0 | -0.73 | 0.05647 | MirTarget; miRNATAP | -0.18 | 0.01418 | NA | |
25 | hsa-miR-194-5p | ALDH1L2 | 1.9 | 0 | -1.12 | 0.02448 | mirMAP | -0.62 | 0 | NA | |
26 | hsa-miR-34a-5p | ALDH1L2 | 1.9 | 0 | -1.12 | 0.02448 | MirTarget | -0.67 | 0 | NA | |
27 | hsa-miR-34a-5p | AMOTL2 | 1.9 | 0 | -1.01 | 0.00015 | MirTarget | -0.31 | 0 | NA | |
28 | hsa-miR-194-5p | ANGPTL1 | 1.9 | 0 | -4.51 | 0 | MirTarget | -0.72 | 0 | NA | |
29 | hsa-miR-34a-5p | ANK2 | 1.9 | 0 | -4.32 | 0 | MirTarget; miRNATAP | -0.92 | 0 | NA | |
30 | hsa-miR-140-5p | ANK3 | 0.84 | 4.0E-5 | -0.29 | 0.31896 | miRanda | -0.2 | 0.00341 | NA | |
31 | hsa-miR-140-5p | ANKRD12 | 0.84 | 4.0E-5 | -0.64 | 0.00012 | miRanda | -0.13 | 0.00079 | NA | |
32 | hsa-miR-140-5p | ANKRD17 | 0.84 | 4.0E-5 | -0.09 | 0.56547 | miRanda | -0.12 | 0.00072 | NA | |
33 | hsa-miR-140-5p | ANKRD34A | 0.84 | 4.0E-5 | -0.41 | 0.07282 | miRanda | -0.15 | 0.00586 | NA | |
34 | hsa-miR-140-5p | ANKS1B | 0.84 | 4.0E-5 | -3.65 | 0 | miRanda | -0.26 | 0.03078 | NA | |
35 | hsa-miR-140-5p | ANO6 | 0.84 | 4.0E-5 | -0.74 | 3.0E-5 | miRanda | -0.17 | 7.0E-5 | NA | |
36 | hsa-miR-34a-5p | ANP32B | 1.9 | 0 | 0.07 | 0.67073 | miRNATAP | -0.12 | 7.0E-5 | NA | |
37 | hsa-miR-34a-5p | AP1S2 | 1.9 | 0 | -1.31 | 0 | MirTarget | -0.43 | 0 | NA | |
38 | hsa-miR-34a-5p | AR | 1.9 | 0 | -3.3 | 0 | MirTarget | -0.29 | 0.02683 | 24349627; 22347519; 21343391; 25920548; 25797256; 23145211 | In this study we found loss of miR-34a which targets AR in PCa tissue specimens especially in patients with higher Gleason grade tumors consistent with increased expression of AR; Most importantly BR-DIM intervention in PCa patients prior to radical prostatectomy showed reexpression of miR-34a which was consistent with decreased expression of AR PSA and Notch-1 in PCa tissue specimens; PCa cells treated with BR-DIM and 5-aza-dC resulted in the demethylation of miR-34a promoter concomitant with inhibition of AR and PSA expression in LNCaP and C4-2B cells; These results suggest for the first time epigenetic silencing of miR-34a in PCa which could be reversed by BR-DIM treatment and thus BR-DIM could be useful for the inactivation of AR in the treatment of PCa.This corrects the article on p;In this study we found loss of miR-34a which targets AR in PCa tissue specimens especially in patients with higher Gleason grade tumors consistent with increased expression of AR; Most importantly BR-DIM intervention in PCa patients prior to radical prostatectomy showed re-expression of miR-34a which was consistent with decreased expression of AR PSA and Notch-1 in PCa tissue specimens; PCa cells treated with BR-DIM and 5-aza-dC resulted in the demethylation of miR-34a promoter concomitant with inhibition of AR and PSA expression in LNCaP and C4-2B cells;In particular analysis of clinical prostate cancers confirmed a negative correlation of miR-34a and miR-34c expression with AR levels;To explore further the possible role of miRNAs in the AR pathway LNCaP cell line was treated with 5α-dihydrotestosterone and flutamide showing alteration in miRNAs expression especially miR-34a which was significantly underexpressed after treatment with high doses of 5α-dihydrotestosterone; Our data support a role for miRNAs especially miR-371 and miR-34a in the complex disarrangement of AR signaling pathway and in the behavior of PC;Repression of miR-34a a known AR-targeting miRNA contributes AR expression by XRN1;Inactivation of AR and Notch 1 signaling by miR 34a attenuates prostate cancer aggressiveness; We found that over-expression of miR-34a led to reduced expression of AR PSA and Notch-1; These findings suggest that the loss of miR-34a is directly linked with up-regulation of AR and Notch-1 both of which are highly expressed in PCa and thus finding innovative approaches by which miR-34a expression could be up-regulated will have a huge impact on the treatment of PCa especially for the treatment of mCRPC |
39 | hsa-miR-34a-5p | ARHGAP1 | 1.9 | 0 | -0.88 | 0 | miRNAWalker2 validate; MirTarget; miRNATAP | -0.18 | 0 | NA | |
40 | hsa-miR-194-5p | ARHGAP21 | 1.9 | 0 | -0.23 | 0.20424 | MirTarget; miRNATAP | -0.13 | 0 | NA | |
41 | hsa-miR-194-5p | ARHGAP24 | 1.9 | 0 | -2.02 | 0 | miRNATAP | -0.46 | 0 | NA | |
42 | hsa-miR-140-5p | ARHGAP32 | 0.84 | 4.0E-5 | 0.68 | 0.00492 | miRanda | -0.16 | 0.00502 | NA | |
43 | hsa-miR-140-5p | ARHGEF4 | 0.84 | 4.0E-5 | -1.44 | 0.0131 | miRanda | -0.48 | 0.00046 | NA | |
44 | hsa-miR-140-5p | ARIH1 | 0.84 | 4.0E-5 | -0.41 | 0.00018 | MirTarget; miRanda | -0.12 | 1.0E-5 | NA | |
45 | hsa-miR-152-3p | ARL6IP1 | -0.05 | 0.84435 | 0.96 | 0 | MirTarget | -0.14 | 5.0E-5 | NA | |
46 | hsa-miR-140-5p | ARMC9 | 0.84 | 4.0E-5 | -0.17 | 0.43502 | miRanda | -0.13 | 0.01514 | NA | |
47 | hsa-miR-140-5p | ARSK | 0.84 | 4.0E-5 | -0.17 | 0.31336 | miRanda | -0.1 | 0.01056 | NA | |
48 | hsa-miR-194-5p | ASAP1 | 1.9 | 0 | 0.06 | 0.77944 | MirTarget; miRNATAP | -0.11 | 0.00108 | NA | |
49 | hsa-miR-34a-5p | ASB1 | 1.9 | 0 | -0.87 | 0 | MirTarget; miRNATAP | -0.16 | 0 | NA | |
50 | hsa-miR-140-5p | ASB5 | 0.84 | 4.0E-5 | -6.18 | 0 | miRanda | -0.99 | 0 | NA | |
51 | hsa-miR-140-5p | ASH1L | 0.84 | 4.0E-5 | -0.67 | 0.00016 | miRanda | -0.26 | 0 | NA | |
52 | hsa-miR-34a-5p | ASTN1 | 1.9 | 0 | -2.34 | 2.0E-5 | MirTarget | -0.25 | 0.01797 | NA | |
53 | hsa-miR-140-5p | ASXL2 | 0.84 | 4.0E-5 | -0.51 | 0.09339 | mirMAP | -0.16 | 0.02429 | NA | |
54 | hsa-miR-34a-5p | ASXL2 | 1.9 | 0 | -0.51 | 0.09339 | MirTarget | -0.27 | 0 | NA | |
55 | hsa-miR-194-5p | ATE1 | 1.9 | 0 | -1.09 | 3.0E-5 | MirTarget | -0.1 | 0.0104 | NA | |
56 | hsa-miR-194-5p | ATF2 | 1.9 | 0 | -0.36 | 0.09137 | miRNATAP | -0.11 | 0.00127 | NA | |
57 | hsa-miR-194-5p | ATL3 | 1.9 | 0 | -0.19 | 0.4343 | MirTarget | -0.21 | 0 | NA | |
58 | hsa-miR-194-5p | ATP8B4 | 1.9 | 0 | -1.9 | 0 | MirTarget | -0.42 | 0 | NA | |
59 | hsa-miR-140-5p | ATP9B | 0.84 | 4.0E-5 | -0.61 | 3.0E-5 | miRanda | -0.1 | 0.00301 | NA | |
60 | hsa-miR-34a-5p | AXIN2 | 1.9 | 0 | -1.7 | 6.0E-5 | miRNAWalker2 validate; miRTarBase | -0.32 | 9.0E-5 | 23624843 | p53 regulates nuclear GSK 3 levels through miR 34 mediated Axin2 suppression in colorectal cancer cells; Exogenous miR-34a decreases Axin2 UTR-reporter activity through multiple binding sites within the 5' and 3' UTR of Axin2; Further RNA transcripts of miR-34 target were correlated with Axin2 in clinical data set of colorectal cancer patients |
61 | hsa-miR-34a-5p | AXL | 1.9 | 0 | -1.77 | 0 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.54 | 0 | 26667302; 21814748; 25895459 | Negative feedback regulation of AXL by miR 34a modulates apoptosis in lung cancer cells; To clarify the role of miRNAs in this regulation loop approaches using bioinformatics and molecular techniques were applied revealing that miR-34a may target the 3' UTR of AXL mRNA to inhibit AXL expression; Therefore we propose that AXL is autoregulated by miR-34a in a feedback loop; this may provide a novel opportunity for developing AXL-targeted anticancer therapies;We identified human miR-34a expression as being >3-fold down from its median expression value across all cell lines in MDA-MB-231 cells and identified AXL as a putative mRNA target using multiple miRNA/target prediction algorithms; In reporter assays miR-34a binds to its putative target site within the AXL 3'UTR to inhibit luciferase expression; Finally we present an inverse correlative trend in miR-34a and AXL expression for both cell line and patient tumor samples;MiR 34a suppresses ovarian cancer proliferation and motility by targeting AXL; Overexpression of miR-34a led to the inhibition of AXL expression indicating that AXL is a target gene for miR-34a; Our data suggest that miR-34a may function as a tumor suppressor through repression of oncogenic AXL in ovarian cancer |
62 | hsa-miR-140-5p | BAG4 | 0.84 | 4.0E-5 | 0.14 | 0.55811 | miRanda | -0.16 | 0.00409 | NA | |
63 | hsa-miR-140-5p | BAZ2B | 0.84 | 4.0E-5 | -0.74 | 3.0E-5 | PITA; miRanda; miRNATAP | -0.27 | 0 | NA | |
64 | hsa-miR-140-5p | BBS4 | 0.84 | 4.0E-5 | 0.02 | 0.87409 | miRanda | -0.13 | 4.0E-5 | NA | |
65 | hsa-miR-140-5p | BBS9 | 0.84 | 4.0E-5 | -0.33 | 0.02266 | miRanda | -0.14 | 3.0E-5 | NA | |
66 | hsa-miR-140-5p | BCHE | 0.84 | 4.0E-5 | -4.37 | 0 | miRanda | -0.52 | 0.00051 | NA | |
67 | hsa-miR-34a-5p | BCL2 | 1.9 | 0 | -2.02 | 0 | miRNAWalker2 validate; miRTarBase | -0.31 | 0 | 24565525; 23155233; 24444609; 20687223; 22623155; 24988056; 18803879; 19714243; 25053345; 20433755; 21399894; 22964582; 23862748 | In vitro and in vivo experiments showed that miR-34a and DOX can be efficiently encapsulated into HA-CS NPs and delivered into tumor cells or tumor tissues and enhance anti-tumor effects of DOX by suppressing the expression of non-pump resistance and anti-apoptosis proto-oncogene Bcl-2;The miR-34a expression levels in cells after irradiation at 30 and 60 Gy were 0.17- and 18.7-times the BCL2 and caspase-9 expression levels respectively;Functional analyses further indicate that restoration of miR-34a inhibits B cell lymphoma-2 Bcl-2 protein expression to withdraw the survival advantage of these resistant NSCLC cells;Thus in PC3PR cells reduced expression of miR-34a confers paclitaxel resistance via up-regulating SIRT1 and Bcl2 expression; MiR-34a and its downstream targets SIRT1 and Bcl2 play important roles in the development of paclitaxel resistance all of which can be useful biomarkers and promising therapeutic targets for the drug resistance in hormone-refractory prostate cancer;MiR 34a inhibits proliferation and migration of breast cancer through down regulation of Bcl 2 and SIRT1; In this study we aimed to determine the effect of miR-34a on the growth of breast cancer and to investigate whether its effect is achieved by targeting Bcl-2 and SIRT1; Bcl-2 and SIRT1 as the targets of miR-34a were found to be in reverse correlation with ectopic expression of miR-34a;Target analysis indicated that micro RNA miR-34a directly regulates Bcl-2 and miR-34a overexpression decreased Bcl-2 protein level in gastric cancer cells; We also found that luteolin upregulates miR-34a expression and downregulates Bcl-2 expression; Based on these results we can draw the conclusion that luteolin partly decreases Bcl-2 expression through upregulating miR-34a expression;miR-34 targets Notch HMGA2 and Bcl-2 genes involved in the self-renewal and survival of cancer stem cells; Human gastric cancer cells were transfected with miR-34 mimics or infected with the lentiviral miR-34-MIF expression system and validated by miR-34 reporter assay using Bcl-2 3'UTR reporter; Human gastric cancer Kato III cells with miR-34 restoration reduced the expression of target genes Bcl-2 Notch and HMGA2; Bcl-2 3'UTR reporter assay showed that the transfected miR-34s were functional and confirmed that Bcl-2 is a direct target of miR-34; The mechanism of miR-34-mediated suppression of self-renewal appears to be related to the direct modulation of downstream targets Bcl-2 Notch and HMGA2 indicating that miR-34 may be involved in gastric cancer stem cell self-renewal/differentiation decision-making;Among the target proteins regulated by miR-34 are Notch pathway proteins and Bcl-2 suggesting the possibility of a role for miR-34 in the maintenance and survival of cancer stem cells; Our data support the view that miR-34 may be involved in pancreatic cancer stem cell self-renewal potentially via the direct modulation of downstream targets Bcl-2 and Notch implying that miR-34 may play an important role in pancreatic cancer stem cell self-renewal and/or cell fate determination;Manipulating miR-34a in prostate cancer cells confirms that this miRNA regulates BCL-2 and may in part regulate response to docetaxel;For instance miR-34a up-regulation corresponded with a down-regulation of BCL2 protein; Treating Par-4-overexpressing HT29 cells with a miR-34a antagomir functionally reversed both BCL2 down-regulation and apoptosis by 5-FU;Quantitative PCR and western analysis confirmed decreased expression of two genes BCL-2 and CCND1 in docetaxel-resistant cells which are both targeted by miR-34a;Tumors harvested from these lungs have elevated levels of oncogenic miRNAs miR-21 and miR-155; are deficient for p53-regulated miRNAs; and have heightened expression of miR-34 target genes such as Met and Bcl-2;MicroRNA 34a targets Bcl 2 and sensitizes human hepatocellular carcinoma cells to sorafenib treatment; HCC tissues with lower miR-34a expression displayed higher expression of Bcl-2 protein than those with high expression of miR-34a; therefore an inverse correlation is evident between the miR-34a level and Bcl-2 expression; Bioinformatics and luciferase reporter assays revealed that miR-34a binds the 3'-UTR of the Bcl-2 mRNA and represses its translation; Western blotting analysis and qRT-PCR confirmed that Bcl-2 is inhibited by miR-34a overexpression; Functional analyses indicated that the restoration of miR-34a reduced cell viability promoted cell apoptosis and potentiated sorafenib-induced apoptosis and toxicity in HCC cell lines by inhibiting Bcl-2 expression |
68 | hsa-miR-140-5p | BCL2L2 | 0.84 | 4.0E-5 | -1.27 | 0 | PITA; miRanda; miRNATAP | -0.2 | 0 | NA | |
69 | hsa-miR-140-5p | BCL9 | 0.84 | 4.0E-5 | 0.12 | 0.4783 | MirTarget; PITA; miRanda; miRNATAP | -0.16 | 8.0E-5 | NA | |
70 | hsa-miR-152-3p | BHLHE41 | -0.05 | 0.84435 | -0.07 | 0.8646 | MirTarget | -0.5 | 0 | NA | |
71 | hsa-miR-194-5p | BICD2 | 1.9 | 0 | -0.46 | 0.01378 | miRNATAP | -0.16 | 0 | NA | |
72 | hsa-miR-34a-5p | BIRC3 | 1.9 | 0 | -1.15 | 0.00716 | miRNAWalker2 validate | -0.22 | 0.0078 | NA | |
73 | hsa-miR-34a-5p | BMP1 | 1.9 | 0 | 0.19 | 0.45337 | mirMAP | -0.15 | 0.0018 | NA | |
74 | hsa-miR-152-3p | BMP3 | -0.05 | 0.84435 | -0.54 | 0.56709 | MirTarget | -1.11 | 0 | NA | |
75 | hsa-miR-140-5p | BMPR1A | 0.84 | 4.0E-5 | -0.77 | 0 | miRanda | -0.2 | 0 | NA | |
76 | hsa-miR-194-5p | BNC1 | 1.9 | 0 | -0.29 | 0.77524 | MirTarget | -1.14 | 0 | NA | |
77 | hsa-miR-34a-5p | BNC2 | 1.9 | 0 | -2.95 | 0 | miRNATAP | -0.8 | 0 | NA | |
78 | hsa-miR-194-5p | BRMS1L | 1.9 | 0 | -0.51 | 0.00391 | MirTarget | -0.19 | 0 | NA | |
79 | hsa-miR-152-3p | BTAF1 | -0.05 | 0.84435 | -0.16 | 0.37827 | MirTarget | -0.14 | 0.00019 | NA | |
80 | hsa-miR-140-5p | BTBD7 | 0.84 | 4.0E-5 | -0.3 | 0.03144 | PITA | -0.17 | 0 | NA | |
81 | hsa-miR-34a-5p | C17orf51 | 1.9 | 0 | -0.68 | 0.02254 | mirMAP | -0.25 | 1.0E-5 | NA | |
82 | hsa-miR-194-5p | C1orf21 | 1.9 | 0 | -1.51 | 0 | mirMAP; miRNATAP | -0.16 | 1.0E-5 | NA | |
83 | hsa-miR-34a-5p | C1orf21 | 1.9 | 0 | -1.51 | 0 | mirMAP | -0.22 | 0 | NA | |
84 | hsa-miR-34a-5p | C3orf70 | 1.9 | 0 | -2.6 | 0 | miRNATAP | -0.47 | 0 | NA | |
85 | hsa-miR-194-5p | C6orf106 | 1.9 | 0 | -0.16 | 0.26914 | mirMAP | -0.11 | 0 | NA | |
86 | hsa-miR-34a-5p | C6orf106 | 1.9 | 0 | -0.16 | 0.26914 | miRNATAP | -0.1 | 0.00011 | NA | |
87 | hsa-miR-152-3p | CABP7 | -0.05 | 0.84435 | 0.93 | 0.03157 | MirTarget | -0.26 | 0.0025 | NA | |
88 | hsa-miR-34a-5p | CACHD1 | 1.9 | 0 | -1.73 | 0 | MirTarget | -0.41 | 0 | NA | |
89 | hsa-miR-140-5p | CACNA1C | 0.84 | 4.0E-5 | -2.53 | 0 | PITA; miRNATAP | -0.34 | 0.00027 | NA | |
90 | hsa-miR-34a-5p | CACNA1C | 1.9 | 0 | -2.53 | 0 | MirTarget | -0.48 | 0 | NA | |
91 | hsa-miR-34a-5p | CALD1 | 1.9 | 0 | -2.47 | 0 | miRNAWalker2 validate | -0.73 | 0 | NA | |
92 | hsa-miR-34a-5p | CAMK2B | 1.9 | 0 | 0.67 | 0.19425 | mirMAP | -0.26 | 0.00749 | NA | |
93 | hsa-miR-140-5p | CAMK2N1 | 0.84 | 4.0E-5 | 0.6 | 0.15571 | PITA; miRanda | -0.35 | 0.00036 | NA | |
94 | hsa-miR-34a-5p | CAPN6 | 1.9 | 0 | -3.48 | 0 | miRNATAP | -0.83 | 0 | NA | |
95 | hsa-miR-140-5p | CASD1 | 0.84 | 4.0E-5 | -0.65 | 0.0001 | miRNAWalker2 validate | -0.11 | 0.0058 | NA | |
96 | hsa-miR-140-5p | CAST | 0.84 | 4.0E-5 | -0.66 | 0.00074 | miRanda | -0.22 | 0 | NA | |
97 | hsa-miR-140-5p | CBR4 | 0.84 | 4.0E-5 | -0.14 | 0.45863 | miRanda | -0.11 | 0.01278 | NA | |
98 | hsa-miR-140-5p | CCDC146 | 0.84 | 4.0E-5 | -0.73 | 0.00616 | miRanda | -0.19 | 0.00226 | NA | |
99 | hsa-miR-34a-5p | CCDC50 | 1.9 | 0 | -0.78 | 0 | miRNATAP | -0.18 | 0 | NA | |
100 | hsa-miR-152-3p | CCDC71 | -0.05 | 0.84435 | 0.3 | 0.02893 | MirTarget | -0.18 | 0 | NA | |
101 | hsa-miR-194-5p | CD302 | 1.9 | 0 | -1.68 | 0 | mirMAP | -0.15 | 0 | NA | |
102 | hsa-miR-34a-5p | CD44 | 1.9 | 0 | -0.8 | 0.04276 | miRNAWalker2 validate; miRTarBase | -0.28 | 0.00023 | 25572695; 24423412; 25551284; 25044638; 21240262; 26231042; 27497057; 23314380 | The c-Myc and CD44 were confirmed as direct targets of miR-34a in EJ cell apoptosis induced by PRE;Furthermore we identified CD44 as being targeted by miR-34a in MIBC cells following cisplatin treatment and increased CD44 expression could efficiently reverse the effect of miR-34a on MIBC cell proliferation colongenic potential and chemosensitivity; Cisplatin-based chemotherapy induced demethylation of miR-34a promoter and increased miR-34a expression which in turn sensitized MIBC cells to cisplatin and decreased the tumorigenicity and proliferation of cancer cells that by reducing the production of CD44;MicroRNA 34a functions as an anti metastatic microRNA and suppresses angiogenesis in bladder cancer by directly targeting CD44; In this study we focus on it that microRNA-34a functions as an anti-metastatic microRNA and suppress angiogenesis in bladder cancer by directly targeting CD44; Our study defines a major metastasis and angiogenesis suppressive role for mir-34a a microRNA functions as a tumor suppressor in bladder cancer by directly targeting CD44 which would be helpful as a therapeutic approach to block bladder cancer metastasis;Nanocomplex-assisted delivery of miR-34a induces cell apoptosis and suppresses migration proliferation and tumor growth of breast cancer cells via targeting CD44 and a Notch-1-signaling pathway;The microRNA miR 34a inhibits prostate cancer stem cells and metastasis by directly repressing CD44; We identified and validated CD44 as a direct and functional target of miR-34a and found that CD44 knockdown phenocopied miR-34a overexpression in inhibiting prostate cancer regeneration and metastasis;Registered report: the microRNA miR 34a inhibits prostate cancer stem cells and metastasis by directly repressing CD44; Tumors with exogenous miR-34a showed reduced levels of CD44 expression Figure 4A and mutation of two putative miR-34a binding sites in the CD33 3' UTR partially abrogated signal repression in a luciferase assay Figure 4D;Nanovesicle mediated systemic delivery of microRNA 34a for CD44 overexpressing gastric cancer stem cell therapy; MicroRNA-34a miR-34a is a promising candidate for CD44 repression-based cancer therapy as it has been reported to inhibit proliferation metastasis and survival of CD44-positive CSCs; Here we used nanovesicles containing PLI/miR complexes NVs/miR to systemically deliver miR-34a and induce miR-34a-triggered CD44 suppression in orthotopically and subcutaneously implanted tumors in nude mice;miR 34a inhibits the metastasis of osteosarcoma cells by repressing the expression of CD44; The ectopic overexpression of miR-34a significantly inhibited the migration and invasive ability of osteosarcoma cells by repressing the expression of CD44; These data suggest that miR-34a plays a tumor suppressor role in the metastasis of osteosarcoma cells by repressing the expression of CD44; Therefore it can be concluded that through the inhibition of CD44 expression levels miR-34a plays a significant role in the migration and invasion of osteosarcoma cells |
103 | hsa-miR-34a-5p | CD47 | 1.9 | 0 | -0.16 | 0.4808 | miRNATAP | -0.2 | 0 | NA | |
104 | hsa-miR-194-5p | CDC42BPA | 1.9 | 0 | -1.41 | 0 | mirMAP | -0.17 | 0 | NA | |
105 | hsa-miR-34a-5p | CDC5L | 1.9 | 0 | -0.01 | 0.91454 | miRNAWalker2 validate | -0.1 | 2.0E-5 | NA | |
106 | hsa-miR-194-5p | CDH2 | 1.9 | 0 | -0.37 | 0.51007 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.65 | 0 | 21845495; 20979124 | The results of real-time PCR and western blot highlighted that miR-194 interacted with N-cadherin and negatively regulated its expression at the translational level;The overexpression of miR-194 in liver mesenchymal-like cancer cells reduced the expression of the mesenchymal cell marker N-cadherin and suppressed invasion and migration of the mesenchymal-like cancer cells both in vitro and in vivo |
107 | hsa-miR-140-5p | CDH26 | 0.84 | 4.0E-5 | 0.92 | 0.14799 | miRanda | -0.3 | 0.04839 | NA | |
108 | hsa-miR-194-5p | CDK14 | 1.9 | 0 | -0.63 | 0.09517 | MirTarget | -0.34 | 0 | NA | |
109 | hsa-miR-152-3p | CDK19 | -0.05 | 0.84435 | -0.08 | 0.56132 | MirTarget | -0.1 | 0.0001 | NA | |
110 | hsa-miR-34a-5p | CDK6 | 1.9 | 0 | -0.77 | 0.06479 | miRNAWalker2 validate; miRTarBase; miRNATAP | -0.52 | 0 | 21702042; 26104764 | Molecular analyses identified Cdk6 and sirtuin SIRT-1 as being targeted by miR-34a in MI-TCC cells however inhibition of Cdk6 and SIRT-1 was not as effective as pre-miR-34a in mediating chemosensitization;The expression of microRNA 34a is inversely correlated with c MET and CDK6 and has a prognostic significance in lung adenocarcinoma patients; We found significant inverse correlations between miR-34a and c-MET R = -0.316 P = 0.028 and CDK6 expression R = -0.4582 P = 0.004 |
111 | hsa-miR-140-5p | CDK8 | 0.84 | 4.0E-5 | -0.22 | 0.28192 | miRanda | -0.15 | 0.00247 | NA | |
112 | hsa-miR-140-5p | CDKL5 | 0.84 | 4.0E-5 | -0.88 | 0.05367 | miRanda | -0.25 | 0.01826 | NA | |
113 | hsa-miR-34a-5p | CDKN1C | 1.9 | 0 | -1.45 | 4.0E-5 | miRNATAP | -0.28 | 3.0E-5 | NA | |
114 | hsa-miR-34a-5p | CDKN2C | 1.9 | 0 | 0.23 | 0.43313 | miRNAWalker2 validate | -0.22 | 6.0E-5 | NA | |
115 | hsa-miR-34a-5p | CDON | 1.9 | 0 | -2.61 | 0 | miRNAWalker2 validate | -0.69 | 0 | NA | |
116 | hsa-miR-34a-5p | CEBPB | 1.9 | 0 | -0.38 | 0.12583 | miRNAWalker2 validate | -0.11 | 0.02632 | NA | |
117 | hsa-miR-34a-5p | CELF2 | 1.9 | 0 | -3.05 | 0 | miRNATAP | -0.63 | 0 | NA | |
118 | hsa-miR-194-5p | CEP170 | 1.9 | 0 | -0.11 | 0.58268 | miRNATAP | -0.15 | 0 | NA | |
119 | hsa-miR-34a-5p | CEP170 | 1.9 | 0 | -0.11 | 0.58268 | miRNAWalker2 validate | -0.25 | 0 | NA | |
120 | hsa-miR-140-5p | CEP350 | 0.84 | 4.0E-5 | -0.04 | 0.77047 | MirTarget; miRanda | -0.14 | 1.0E-5 | NA | |
121 | hsa-miR-140-5p | CHD6 | 0.84 | 4.0E-5 | -0.22 | 0.2394 | miRanda | -0.14 | 0.00233 | NA | |
122 | hsa-miR-194-5p | CHD9 | 1.9 | 0 | -0.8 | 1.0E-5 | miRNATAP | -0.13 | 0 | NA | |
123 | hsa-miR-140-5p | CHIC1 | 0.84 | 4.0E-5 | -1.03 | 0 | miRanda | -0.2 | 1.0E-5 | NA | |
124 | hsa-miR-34a-5p | CHM | 1.9 | 0 | -0.35 | 0.02247 | MirTarget | -0.15 | 0 | NA | |
125 | hsa-miR-194-5p | CIITA | 1.9 | 0 | -0.02 | 0.95968 | mirMAP | -0.21 | 0.0028 | NA | |
126 | hsa-miR-34a-5p | CKAP5 | 1.9 | 0 | 0.47 | 0.00244 | miRNAWalker2 validate | -0.11 | 0.00011 | NA | |
127 | hsa-miR-194-5p | CLIP4 | 1.9 | 0 | -1.61 | 0 | MirTarget | -0.46 | 0 | NA | |
128 | hsa-miR-34a-5p | CLOCK | 1.9 | 0 | -0.51 | 0.03689 | MirTarget | -0.2 | 1.0E-5 | NA | |
129 | hsa-miR-34a-5p | CNST | 1.9 | 0 | -0.93 | 0 | MirTarget | -0.15 | 0 | NA | |
130 | hsa-miR-140-5p | CNTN1 | 0.84 | 4.0E-5 | -4.98 | 0 | PITA; miRanda | -0.87 | 1.0E-5 | NA | |
131 | hsa-miR-34a-5p | CNTN2 | 1.9 | 0 | -3.83 | 0 | MirTarget; miRNATAP | -0.54 | 0 | NA | |
132 | hsa-miR-34a-5p | CNTNAP1 | 1.9 | 0 | -1.47 | 0 | MirTarget; miRNATAP | -0.36 | 0 | NA | |
133 | hsa-miR-34a-5p | CNTNAP2 | 1.9 | 0 | -1.31 | 0.11505 | miRNATAP | -0.67 | 2.0E-5 | NA | |
134 | hsa-miR-34a-5p | COL12A1 | 1.9 | 0 | 0.61 | 0.13434 | MirTarget; miRNATAP | -0.28 | 0.00031 | NA | |
135 | hsa-miR-34a-5p | COL5A2 | 1.9 | 0 | 0.19 | 0.64093 | MirTarget | -0.41 | 0 | NA | |
136 | hsa-miR-34a-5p | CORO1C | 1.9 | 0 | -1.12 | 0 | MirTarget; miRNATAP | -0.39 | 0 | NA | |
137 | hsa-miR-34a-5p | CPEB2 | 1.9 | 0 | -1.81 | 0 | miRNATAP | -0.29 | 0 | NA | |
138 | hsa-miR-34a-5p | CPEB3 | 1.9 | 0 | -1.3 | 0 | miRNATAP | -0.15 | 7.0E-5 | NA | |
139 | hsa-miR-34a-5p | CR2 | 1.9 | 0 | -1.53 | 0.0725 | MirTarget | -0.79 | 0 | NA | |
140 | hsa-miR-34a-5p | CREB5 | 1.9 | 0 | -2.28 | 0 | miRNATAP | -0.5 | 0 | NA | |
141 | hsa-miR-34a-5p | CRY2 | 1.9 | 0 | -1.68 | 0 | MirTarget | -0.17 | 0 | NA | |
142 | hsa-miR-140-5p | CRYAB | 0.84 | 4.0E-5 | -3.8 | 0 | miRanda | -0.34 | 0.00352 | NA | |
143 | hsa-miR-140-5p | CRYBG3 | 0.84 | 4.0E-5 | -1.11 | 5.0E-5 | miRanda | -0.13 | 0.0437 | NA | |
144 | hsa-miR-140-5p | CSDE1 | 0.84 | 4.0E-5 | -0.72 | 0 | miRanda | -0.18 | 0 | NA | |
145 | hsa-miR-34a-5p | CSF1R | 1.9 | 0 | -1.05 | 0.01797 | MirTarget; miRNATAP | -0.46 | 0 | NA | |
146 | hsa-miR-34a-5p | CTCFL | 1.9 | 0 | 0.39 | 0.13775 | MirTarget | -0.13 | 0.01043 | NA | |
147 | hsa-miR-34a-5p | CTDSP2 | 1.9 | 0 | -0.39 | 0.00969 | miRNATAP | -0.22 | 0 | NA | |
148 | hsa-miR-140-5p | CTNNA1 | 0.84 | 4.0E-5 | -0.28 | 0.01517 | miRanda | -0.12 | 3.0E-5 | NA | |
149 | hsa-miR-140-5p | CTNNA3 | 0.84 | 4.0E-5 | -1.94 | 0.00013 | miRanda | -0.25 | 0.03981 | NA | |
150 | hsa-miR-140-5p | CTSF | 0.84 | 4.0E-5 | -1.38 | 0 | miRanda | -0.15 | 0.02452 | NA |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | NEUROGENESIS | 124 | 1402 | 1.072e-17 | 4.988e-14 |
2 | REGULATION OF CELL DIFFERENTIATION | 125 | 1492 | 5.353e-16 | 1.033e-12 |
3 | CELL DEVELOPMENT | 121 | 1426 | 6.66e-16 | 1.033e-12 |
4 | TISSUE DEVELOPMENT | 122 | 1518 | 2.695e-14 | 3.135e-11 |
5 | CELL PROJECTION ORGANIZATION | 85 | 902 | 8.181e-14 | 7.613e-11 |
6 | MOVEMENT OF CELL OR SUBCELLULAR COMPONENT | 105 | 1275 | 4.956e-13 | 3.524e-10 |
7 | CELLULAR COMPONENT MORPHOGENESIS | 83 | 900 | 5.302e-13 | 3.524e-10 |
8 | CENTRAL NERVOUS SYSTEM DEVELOPMENT | 81 | 872 | 7.1e-13 | 4.13e-10 |
9 | REGULATION OF MULTICELLULAR ORGANISMAL DEVELOPMENT | 126 | 1672 | 9.796e-13 | 5.065e-10 |
10 | NEURON DIFFERENTIATION | 80 | 874 | 2.132e-12 | 9.918e-10 |
11 | INTRACELLULAR SIGNAL TRANSDUCTION | 118 | 1572 | 7.623e-12 | 3.224e-09 |
12 | REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 122 | 1656 | 1.097e-11 | 3.676e-09 |
13 | REGULATION OF ANATOMICAL STRUCTURE MORPHOGENESIS | 87 | 1021 | 1.042e-11 | 3.676e-09 |
14 | REGULATION OF CELL DEVELOPMENT | 76 | 836 | 1.106e-11 | 3.676e-09 |
15 | HEAD DEVELOPMENT | 68 | 709 | 1.364e-11 | 4.232e-09 |
16 | NEURON PROJECTION DEVELOPMENT | 56 | 545 | 6.991e-11 | 2.033e-08 |
17 | REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 126 | 1784 | 7.895e-11 | 2.161e-08 |
18 | POSITIVE REGULATION OF DEVELOPMENTAL PROCESS | 91 | 1142 | 1.236e-10 | 3.194e-08 |
19 | NEURON DEVELOPMENT | 64 | 687 | 1.903e-10 | 4.66e-08 |
20 | CELL PART MORPHOGENESIS | 60 | 633 | 3.676e-10 | 8.551e-08 |
21 | ANATOMICAL STRUCTURE FORMATION INVOLVED IN MORPHOGENESIS | 79 | 957 | 4.553e-10 | 1.009e-07 |
22 | PROTEIN PHOSPHORYLATION | 78 | 944 | 5.672e-10 | 1.2e-07 |
23 | REGULATION OF PHOSPHORUS METABOLIC PROCESS | 114 | 1618 | 8.535e-10 | 1.727e-07 |
24 | REGULATION OF NEURON DIFFERENTIATION | 53 | 554 | 2.94e-09 | 5.7e-07 |
25 | NEGATIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 64 | 740 | 3.796e-09 | 7.064e-07 |
26 | ORGAN MORPHOGENESIS | 69 | 841 | 7.974e-09 | 1.427e-06 |
27 | POSITIVE REGULATION OF CELL COMMUNICATION | 106 | 1532 | 9.684e-09 | 1.581e-06 |
28 | FOREBRAIN DEVELOPMENT | 39 | 357 | 1.073e-08 | 1.581e-06 |
29 | REGULATION OF CELL PROJECTION ORGANIZATION | 52 | 558 | 1.012e-08 | 1.581e-06 |
30 | MUSCLE STRUCTURE DEVELOPMENT | 44 | 432 | 1.047e-08 | 1.581e-06 |
31 | NEURON PROJECTION MORPHOGENESIS | 42 | 402 | 1.087e-08 | 1.581e-06 |
32 | LOCOMOTION | 84 | 1114 | 9.184e-09 | 1.581e-06 |
33 | CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 49 | 513 | 1.24e-08 | 1.749e-06 |
34 | REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 63 | 750 | 1.534e-08 | 2.099e-06 |
35 | POSITIVE REGULATION OF NEURON DIFFERENTIATION | 35 | 306 | 1.91e-08 | 2.469e-06 |
36 | REGULATION OF CELL MORPHOGENESIS | 51 | 552 | 1.867e-08 | 2.469e-06 |
37 | POSITIVE REGULATION OF MOLECULAR FUNCTION | 118 | 1791 | 2.04e-08 | 2.565e-06 |
38 | REGULATION OF ACTIN FILAMENT BASED PROCESS | 35 | 312 | 3.131e-08 | 3.834e-06 |
39 | REGULATION OF PROTEIN MODIFICATION PROCESS | 113 | 1710 | 3.655e-08 | 4.328e-06 |
40 | ESTABLISHMENT OR MAINTENANCE OF CELL POLARITY | 22 | 141 | 3.72e-08 | 4.328e-06 |
41 | POSITIVE REGULATION OF GENE EXPRESSION | 114 | 1733 | 4.021e-08 | 4.563e-06 |
42 | TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 60 | 724 | 5.541e-08 | 6.139e-06 |
43 | SENSORY ORGAN DEVELOPMENT | 46 | 493 | 7.034e-08 | 7.611e-06 |
44 | CELL MORPHOGENESIS INVOLVED IN NEURON DIFFERENTIATION | 38 | 368 | 7.434e-08 | 7.861e-06 |
45 | CYTOSKELETON ORGANIZATION | 66 | 838 | 8.095e-08 | 8.371e-06 |
46 | POSITIVE REGULATION OF CELL DIFFERENTIATION | 65 | 823 | 9.205e-08 | 9.311e-06 |
47 | REGULATION OF HYDROLASE ACTIVITY | 92 | 1327 | 9.451e-08 | 9.357e-06 |
48 | REGULATION OF CELLULAR COMPONENT MOVEMENT | 62 | 771 | 9.773e-08 | 9.474e-06 |
49 | REGULATION OF TRANSPORT | 116 | 1804 | 1.019e-07 | 9.676e-06 |
50 | CELLULAR RESPONSE TO ENDOGENOUS STIMULUS | 75 | 1008 | 1.045e-07 | 9.727e-06 |
51 | REGULATION OF NEURON PROJECTION DEVELOPMENT | 40 | 408 | 1.378e-07 | 1.257e-05 |
52 | REGULATION OF MUSCLE CELL DIFFERENTIATION | 22 | 152 | 1.469e-07 | 1.314e-05 |
53 | POSITIVE REGULATION OF CELL PROJECTION ORGANIZATION | 33 | 303 | 1.56e-07 | 1.369e-05 |
54 | NEURON PROJECTION GUIDANCE | 26 | 205 | 1.685e-07 | 1.426e-05 |
55 | PHOSPHORYLATION | 86 | 1228 | 1.676e-07 | 1.426e-05 |
56 | RESPONSE TO ENDOGENOUS STIMULUS | 97 | 1450 | 2.2e-07 | 1.828e-05 |
57 | NEURON MIGRATION | 18 | 110 | 3.078e-07 | 2.513e-05 |
58 | REGULATION OF GTPASE ACTIVITY | 55 | 673 | 3.166e-07 | 2.54e-05 |
59 | EPITHELIUM DEVELOPMENT | 70 | 945 | 3.372e-07 | 2.559e-05 |
60 | CELLULAR RESPONSE TO OXYGEN CONTAINING COMPOUND | 62 | 799 | 3.41e-07 | 2.559e-05 |
61 | CELL MOTILITY | 64 | 835 | 3.383e-07 | 2.559e-05 |
62 | LOCALIZATION OF CELL | 64 | 835 | 3.383e-07 | 2.559e-05 |
63 | POSITIVE REGULATION OF TRANSCRIPTION FROM RNA POLYMERASE II PROMOTER | 73 | 1004 | 3.802e-07 | 2.808e-05 |
64 | PHOSPHATE CONTAINING COMPOUND METABOLIC PROCESS | 122 | 1977 | 4.166e-07 | 3.028e-05 |
65 | CARDIOVASCULAR SYSTEM DEVELOPMENT | 61 | 788 | 4.616e-07 | 3.254e-05 |
66 | CIRCULATORY SYSTEM DEVELOPMENT | 61 | 788 | 4.616e-07 | 3.254e-05 |
67 | POSITIVE REGULATION OF MULTICELLULAR ORGANISMAL PROCESS | 93 | 1395 | 4.687e-07 | 3.255e-05 |
68 | POSITIVE REGULATION OF RESPONSE TO STIMULUS | 119 | 1929 | 6.032e-07 | 4.128e-05 |
69 | MUSCLE ORGAN DEVELOPMENT | 30 | 277 | 6.405e-07 | 4.319e-05 |
70 | HEART DEVELOPMENT | 42 | 466 | 6.62e-07 | 4.4e-05 |
71 | POSITIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 40 | 437 | 8.255e-07 | 5.41e-05 |
72 | EAR DEVELOPMENT | 24 | 195 | 8.675e-07 | 5.564e-05 |
73 | REGULATION OF CELLULAR LOCALIZATION | 86 | 1277 | 8.73e-07 | 5.564e-05 |
74 | REGULATION OF MAPK CASCADE | 53 | 660 | 8.914e-07 | 5.605e-05 |
75 | POSITIVE REGULATION OF CELL DEVELOPMENT | 42 | 472 | 9.266e-07 | 5.749e-05 |
76 | NEGATIVE REGULATION OF CELL DIFFERENTIATION | 50 | 609 | 9.614e-07 | 5.886e-05 |
77 | POSITIVE REGULATION OF BIOSYNTHETIC PROCESS | 112 | 1805 | 1.032e-06 | 6.239e-05 |
78 | NEGATIVE REGULATION OF CELL COMMUNICATION | 81 | 1192 | 1.314e-06 | 7.839e-05 |
79 | TELENCEPHALON DEVELOPMENT | 26 | 228 | 1.345e-06 | 7.919e-05 |
80 | TAXIS | 41 | 464 | 1.492e-06 | 8.679e-05 |
81 | REGULATION OF CYTOPLASMIC TRANSPORT | 42 | 481 | 1.513e-06 | 8.694e-05 |
82 | MUSCLE TISSUE DEVELOPMENT | 29 | 275 | 1.692e-06 | 9.486e-05 |
83 | NEGATIVE REGULATION OF DEVELOPMENTAL PROCESS | 60 | 801 | 1.687e-06 | 9.486e-05 |
84 | REGULATION OF CELL MORPHOGENESIS INVOLVED IN DIFFERENTIATION | 33 | 337 | 1.754e-06 | 9.6e-05 |
85 | POSITIVE REGULATION OF INTRACELLULAR SIGNAL TRANSDUCTION | 64 | 876 | 1.752e-06 | 9.6e-05 |
86 | POSITIVE REGULATION OF NEURON PROJECTION DEVELOPMENT | 26 | 232 | 1.868e-06 | 0.0001011 |
87 | POSITIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 72 | 1036 | 2.397e-06 | 0.0001268 |
88 | POSITIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 72 | 1036 | 2.397e-06 | 0.0001268 |
89 | NEGATIVE REGULATION OF GENE EXPRESSION | 95 | 1493 | 2.662e-06 | 0.0001392 |
90 | REGULATION OF MUSCLE SYSTEM PROCESS | 23 | 195 | 3.051e-06 | 0.0001577 |
91 | ENZYME LINKED RECEPTOR PROTEIN SIGNALING PATHWAY | 53 | 689 | 3.205e-06 | 0.0001639 |
92 | EMBRYO DEVELOPMENT | 64 | 894 | 3.435e-06 | 0.0001737 |
93 | CEREBRAL CORTEX DEVELOPMENT | 16 | 105 | 3.653e-06 | 0.0001828 |
94 | FAT CELL DIFFERENTIATION | 16 | 106 | 4.147e-06 | 0.0002053 |
95 | ACTIN FILAMENT BASED PROCESS | 39 | 450 | 4.272e-06 | 0.0002092 |
96 | REGULATION OF CYTOSKELETON ORGANIZATION | 42 | 502 | 4.472e-06 | 0.0002167 |
97 | POSITIVE REGULATION OF MUSCLE CELL DIFFERENTIATION | 14 | 84 | 5.03e-06 | 0.0002388 |
98 | EMBRYONIC MORPHOGENESIS | 44 | 539 | 5.008e-06 | 0.0002388 |
99 | POSITIVE REGULATION OF HYDROLASE ACTIVITY | 64 | 905 | 5.111e-06 | 0.0002402 |
100 | POSITIVE REGULATION OF CATALYTIC ACTIVITY | 95 | 1518 | 5.323e-06 | 0.0002452 |
101 | CELLULAR RESPONSE TO ORGANIC SUBSTANCE | 111 | 1848 | 5.303e-06 | 0.0002452 |
102 | SKELETAL SYSTEM DEVELOPMENT | 39 | 455 | 5.551e-06 | 0.0002532 |
103 | RESPONSE TO OXYGEN CONTAINING COMPOUND | 88 | 1381 | 6.089e-06 | 0.000275 |
104 | RESPONSE TO GROWTH FACTOR | 40 | 475 | 6.453e-06 | 0.0002887 |
105 | REGULATION OF MEMBRANE POTENTIAL | 32 | 343 | 6.939e-06 | 0.0003075 |
106 | TISSUE MORPHOGENESIS | 43 | 533 | 8.592e-06 | 0.0003772 |
107 | REGULATION OF HOMEOSTATIC PROCESS | 38 | 447 | 8.825e-06 | 0.0003838 |
108 | TUBE DEVELOPMENT | 44 | 552 | 9.151e-06 | 0.0003941 |
109 | ENDOMEMBRANE SYSTEM ORGANIZATION | 39 | 465 | 9.232e-06 | 0.0003941 |
110 | PALLIUM DEVELOPMENT | 19 | 153 | 1.032e-05 | 0.0004366 |
111 | NEGATIVE REGULATION OF RESPONSE TO STIMULUS | 86 | 1360 | 1.048e-05 | 0.0004393 |
112 | NEGATIVE REGULATION OF PHOSPHORUS METABOLIC PROCESS | 43 | 541 | 1.239e-05 | 0.0005101 |
113 | NEGATIVE REGULATION OF PHOSPHATE METABOLIC PROCESS | 43 | 541 | 1.239e-05 | 0.0005101 |
114 | REGULATION OF SYSTEM PROCESS | 41 | 507 | 1.312e-05 | 0.0005354 |
115 | PROTEIN LOCALIZATION | 107 | 1805 | 1.418e-05 | 0.0005736 |
116 | NEGATIVE REGULATION OF NITROGEN COMPOUND METABOLIC PROCESS | 93 | 1517 | 1.53e-05 | 0.0006138 |
117 | POSITIVE REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 9 | 39 | 1.664e-05 | 0.0006618 |
118 | EYE DEVELOPMENT | 30 | 326 | 1.738e-05 | 0.0006852 |
119 | STRIATED MUSCLE CELL DIFFERENTIATION | 20 | 173 | 1.784e-05 | 0.0006977 |
120 | GROWTH | 35 | 410 | 1.815e-05 | 0.0007037 |
121 | CELLULAR RESPONSE TO ACID CHEMICAL | 20 | 175 | 2.113e-05 | 0.0008127 |
122 | RHYTHMIC PROCESS | 28 | 298 | 2.254e-05 | 0.0008597 |
123 | NEGATIVE REGULATION OF PROTEIN METABOLIC PROCESS | 71 | 1087 | 2.304e-05 | 0.0008715 |
124 | NEGATIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 50 | 684 | 2.392e-05 | 0.0008977 |
125 | REGULATION OF HEART CONTRACTION | 23 | 221 | 2.427e-05 | 0.0009036 |
126 | POSITIVE REGULATION OF CELLULAR COMPONENT ORGANIZATION | 74 | 1152 | 2.688e-05 | 0.0009904 |
127 | MODULATION OF SYNAPTIC TRANSMISSION | 28 | 301 | 2.703e-05 | 0.0009904 |
128 | GLAND MORPHOGENESIS | 14 | 97 | 2.755e-05 | 0.001002 |
129 | CELLULAR MACROMOLECULE LOCALIZATION | 78 | 1234 | 2.813e-05 | 0.001014 |
130 | CONNECTIVE TISSUE DEVELOPMENT | 21 | 194 | 3.021e-05 | 0.001081 |
131 | NEGATIVE REGULATION OF CELL DEVELOPMENT | 28 | 303 | 3.046e-05 | 0.001082 |
132 | IMMUNE SYSTEM DEVELOPMENT | 44 | 582 | 3.331e-05 | 0.00115 |
133 | RESPONSE TO EXTERNAL STIMULUS | 106 | 1821 | 3.336e-05 | 0.00115 |
134 | NEGATIVE REGULATION OF PHOSPHORYLATION | 35 | 422 | 3.316e-05 | 0.00115 |
135 | REGULATION OF MUSCLE ADAPTATION | 11 | 63 | 3.284e-05 | 0.00115 |
136 | REGULATION OF INTRACELLULAR TRANSPORT | 46 | 621 | 3.662e-05 | 0.001253 |
137 | CELL FATE COMMITMENT | 23 | 227 | 3.714e-05 | 0.001261 |
138 | MEMBRANE ASSEMBLY | 7 | 25 | 3.825e-05 | 0.00129 |
139 | REGULATION OF PROTEIN LOCALIZATION | 63 | 950 | 4.33e-05 | 0.001449 |
140 | REGULATION OF EMBRYONIC DEVELOPMENT | 15 | 114 | 4.387e-05 | 0.001458 |
141 | VENTRICULAR SYSTEM DEVELOPMENT | 7 | 26 | 5.056e-05 | 0.001669 |
142 | CELL PROJECTION ASSEMBLY | 25 | 264 | 5.366e-05 | 0.001758 |
143 | PLASMA MEMBRANE ORGANIZATION | 21 | 203 | 5.903e-05 | 0.001921 |
144 | LATERAL VENTRICLE DEVELOPMENT | 5 | 12 | 6.037e-05 | 0.001951 |
145 | MORPHOGENESIS OF AN EPITHELIUM | 33 | 400 | 6.12e-05 | 0.001964 |
146 | COGNITION | 24 | 251 | 6.452e-05 | 0.002056 |
147 | REGULATION OF CELL DEATH | 88 | 1472 | 6.554e-05 | 0.002075 |
148 | PEPTIDYL THREONINE MODIFICATION | 9 | 46 | 6.75e-05 | 0.002122 |
149 | REGULATION OF CELL PROLIFERATION | 89 | 1496 | 7.067e-05 | 0.002207 |
150 | CIRCADIAN REGULATION OF GENE EXPRESSION | 10 | 57 | 7.15e-05 | 0.002218 |
151 | MUSCLE CELL DIFFERENTIATION | 23 | 237 | 7.255e-05 | 0.002229 |
152 | RESPONSE TO OXIDATIVE STRESS | 30 | 352 | 7.281e-05 | 0.002229 |
153 | ACTIN FILAMENT BASED MOVEMENT | 13 | 93 | 7.432e-05 | 0.00226 |
154 | PEPTIDYL SERINE MODIFICATION | 17 | 148 | 8.079e-05 | 0.002436 |
155 | AXON EXTENSION | 8 | 37 | 8.116e-05 | 0.002436 |
156 | BIOLOGICAL ADHESION | 66 | 1032 | 8.438e-05 | 0.002517 |
157 | REGULATION OF PROTEIN KINASE B SIGNALING | 15 | 121 | 8.798e-05 | 0.002608 |
158 | POSITIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 71 | 1135 | 8.987e-05 | 0.002646 |
159 | TUBE MORPHOGENESIS | 28 | 323 | 9.373e-05 | 0.002743 |
160 | GLIAL CELL DIFFERENTIATION | 16 | 136 | 9.757e-05 | 0.002837 |
161 | PROTEIN LOCALIZATION TO CELL PERIPHERY | 17 | 151 | 0.0001038 | 0.003 |
162 | SKELETAL MUSCLE ORGAN DEVELOPMENT | 16 | 137 | 0.0001065 | 0.003059 |
163 | REGULATION OF SMALL GTPASE MEDIATED SIGNAL TRANSDUCTION | 25 | 278 | 0.0001232 | 0.003516 |
164 | CELLULAR RESPONSE TO NITROGEN COMPOUND | 38 | 505 | 0.0001244 | 0.003531 |
165 | REGULATION OF STRIATED MUSCLE CELL DIFFERENTIATION | 12 | 85 | 0.0001265 | 0.003568 |
166 | MEMBRANE BIOGENESIS | 7 | 30 | 0.0001363 | 0.00382 |
167 | MICROTUBULE CYTOSKELETON ORGANIZATION | 29 | 348 | 0.0001411 | 0.003932 |
168 | NEGATIVE REGULATION OF CELL DEATH | 57 | 872 | 0.0001465 | 0.004059 |
169 | BONE DEVELOPMENT | 17 | 156 | 0.000155 | 0.004268 |
170 | DEVELOPMENTAL GROWTH | 28 | 333 | 0.0001572 | 0.004304 |
171 | BONE CELL DEVELOPMENT | 6 | 22 | 0.0001637 | 0.004404 |
172 | REGULATION OF ORGANELLE ORGANIZATION | 72 | 1178 | 0.0001622 | 0.004404 |
173 | SUBPALLIUM DEVELOPMENT | 6 | 22 | 0.0001637 | 0.004404 |
174 | REGULATION OF PHOSPHATASE ACTIVITY | 15 | 128 | 0.0001667 | 0.004445 |
175 | SIGNAL TRANSDUCTION BY PROTEIN PHOSPHORYLATION | 32 | 404 | 0.0001672 | 0.004445 |
176 | POSITIVE REGULATION OF PROTEIN METABOLIC PROCESS | 87 | 1492 | 0.0001696 | 0.004483 |
177 | OSSIFICATION | 23 | 251 | 0.000172 | 0.004521 |
178 | ESTABLISHMENT OF CELL POLARITY | 12 | 88 | 0.0001772 | 0.004633 |
179 | MYELOID CELL DIFFERENTIATION | 19 | 189 | 0.0001901 | 0.004943 |
180 | STEM CELL DIFFERENTIATION | 19 | 190 | 0.0002036 | 0.005264 |
181 | NEURON PROJECTION EXTENSION | 9 | 53 | 0.000212 | 0.00545 |
182 | REGULATION OF CELLULAR COMPONENT BIOGENESIS | 51 | 767 | 0.0002172 | 0.005541 |
183 | RESPONSE TO REACTIVE OXYGEN SPECIES | 19 | 191 | 0.0002179 | 0.005541 |
184 | ESTABLISHMENT OF LOCALIZATION IN CELL | 95 | 1676 | 0.0002293 | 0.005799 |
185 | CARTILAGE DEVELOPMENT | 16 | 147 | 0.000243 | 0.006048 |
186 | MICROTUBULE BASED PROCESS | 38 | 522 | 0.0002425 | 0.006048 |
187 | ENSHEATHMENT OF NEURONS | 12 | 91 | 0.0002444 | 0.006048 |
188 | AXON ENSHEATHMENT | 12 | 91 | 0.0002444 | 0.006048 |
189 | GLAND DEVELOPMENT | 31 | 395 | 0.000247 | 0.006052 |
190 | REGULATION OF INSULIN RECEPTOR SIGNALING PATHWAY | 8 | 43 | 0.0002471 | 0.006052 |
191 | REGULATION OF METAL ION TRANSPORT | 27 | 325 | 0.0002484 | 0.006052 |
192 | ODONTOGENESIS | 13 | 105 | 0.0002587 | 0.00627 |
193 | POSITIVE REGULATION OF CELL GROWTH | 16 | 148 | 0.0002627 | 0.006334 |
194 | VASCULATURE DEVELOPMENT | 35 | 469 | 0.0002657 | 0.006373 |
195 | RESPONSE TO HORMONE | 57 | 893 | 0.0002697 | 0.006435 |
196 | REGULATION OF STRIATED MUSCLE CONTRACTION | 11 | 79 | 0.0002713 | 0.006441 |
197 | REGULATION OF MYELOID CELL APOPTOTIC PROCESS | 6 | 24 | 0.000276 | 0.00652 |
198 | POSITIVE REGULATION OF PHOSPHOPROTEIN PHOSPHATASE ACTIVITY | 5 | 16 | 0.0002917 | 0.006786 |
199 | MEGAKARYOCYTE DEVELOPMENT | 5 | 16 | 0.0002917 | 0.006786 |
200 | STRIATUM DEVELOPMENT | 5 | 16 | 0.0002917 | 0.006786 |
201 | CELL GROWTH | 15 | 135 | 0.0003005 | 0.006957 |
202 | SINGLE ORGANISM CELLULAR LOCALIZATION | 57 | 898 | 0.0003103 | 0.007148 |
203 | NEGATIVE REGULATION OF NERVOUS SYSTEM DEVELOPMENT | 23 | 262 | 0.0003207 | 0.007351 |
204 | CELLULAR COMPONENT ASSEMBLY INVOLVED IN MORPHOGENESIS | 22 | 246 | 0.000332 | 0.007572 |
205 | SINGLE ORGANISM BEHAVIOR | 30 | 384 | 0.0003337 | 0.007573 |
206 | REGULATION OF TRANSPORTER ACTIVITY | 19 | 198 | 0.0003451 | 0.007795 |
207 | CIRCADIAN RHYTHM | 15 | 137 | 0.0003527 | 0.007927 |
208 | REGULATION OF CELLULAR PROTEIN LOCALIZATION | 39 | 552 | 0.0003672 | 0.008213 |
209 | REGULATION OF PHOSPHATIDYLINOSITOL 3 KINASE SIGNALING | 15 | 138 | 0.0003815 | 0.008493 |
210 | BEHAVIOR | 37 | 516 | 0.0003892 | 0.008583 |
211 | CELLULAR RESPONSE TO OXIDATIVE STRESS | 18 | 184 | 0.0003876 | 0.008583 |
212 | EMBRYO DEVELOPMENT ENDING IN BIRTH OR EGG HATCHING | 39 | 554 | 0.0003942 | 0.008652 |
213 | ANATOMICAL STRUCTURE ARRANGEMENT | 5 | 17 | 0.0003998 | 0.008693 |
214 | MYELIN ASSEMBLY | 5 | 17 | 0.0003998 | 0.008693 |
215 | MAINTENANCE OF LOCATION IN CELL | 12 | 96 | 0.0004041 | 0.008706 |
216 | CARDIOCYTE DIFFERENTIATION | 12 | 96 | 0.0004041 | 0.008706 |
217 | REGULATION OF ION HOMEOSTASIS | 19 | 201 | 0.0004169 | 0.008939 |
218 | REGULATION OF EPITHELIAL CELL PROLIFERATION | 24 | 285 | 0.0004418 | 0.009431 |
219 | POSITIVE REGULATION OF AXON EXTENSION | 7 | 36 | 0.0004545 | 0.009656 |
220 | NEGATIVE REGULATION OF PROTEIN MODIFICATION PROCESS | 42 | 616 | 0.0004632 | 0.009796 |
221 | POSITIVE REGULATION OF DEPHOSPHORYLATION | 8 | 47 | 0.0004661 | 0.009814 |
222 | POSITIVE REGULATION OF DEVELOPMENTAL GROWTH | 16 | 156 | 0.000476 | 0.009977 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | ENZYME BINDING | 133 | 1737 | 6.055e-14 | 5.625e-11 |
2 | CYTOSKELETAL PROTEIN BINDING | 71 | 819 | 4.565e-10 | 2.121e-07 |
3 | RNA POLYMERASE II TRANSCRIPTION FACTOR ACTIVITY SEQUENCE SPECIFIC DNA BINDING | 59 | 629 | 7.753e-10 | 2.401e-07 |
4 | BETA CATENIN BINDING | 18 | 84 | 3.857e-09 | 8.958e-07 |
5 | NUCLEIC ACID BINDING TRANSCRIPTION FACTOR ACTIVITY | 89 | 1199 | 6.764e-09 | 1.257e-06 |
6 | KINASE BINDING | 55 | 606 | 9.504e-09 | 1.472e-06 |
7 | ACTIN BINDING | 41 | 393 | 1.697e-08 | 2.252e-06 |
8 | KINASE ACTIVITY | 67 | 842 | 4.348e-08 | 5.049e-06 |
9 | PROTEIN KINASE ACTIVITY | 55 | 640 | 6.117e-08 | 5.958e-06 |
10 | TRANSCRIPTION FACTOR BINDING | 48 | 524 | 6.414e-08 | 5.958e-06 |
11 | REGULATORY REGION NUCLEIC ACID BINDING | 65 | 818 | 7.353e-08 | 6.21e-06 |
12 | ACTIVATING TRANSCRIPTION FACTOR BINDING | 13 | 57 | 2.604e-07 | 2.016e-05 |
13 | TRANSCRIPTION FACTOR ACTIVITY RNA POLYMERASE II CORE PROMOTER PROXIMAL REGION SEQUENCE SPECIFIC BINDING | 34 | 328 | 3.293e-07 | 2.353e-05 |
14 | PROTEIN SERINE THREONINE KINASE ACTIVITY | 41 | 445 | 5.072e-07 | 3.366e-05 |
15 | MACROMOLECULAR COMPLEX BINDING | 92 | 1399 | 9.815e-07 | 5.735e-05 |
16 | TRANSFERASE ACTIVITY TRANSFERRING PHOSPHORUS CONTAINING GROUPS | 71 | 992 | 9.877e-07 | 5.735e-05 |
17 | TRANSCRIPTIONAL ACTIVATOR ACTIVITY RNA POLYMERASE II TRANSCRIPTION REGULATORY REGION SEQUENCE SPECIFIC BINDING | 32 | 315 | 1.135e-06 | 6.202e-05 |
18 | SEQUENCE SPECIFIC DNA BINDING | 71 | 1037 | 4.758e-06 | 0.0002456 |
19 | TRANSMEMBRANE RECEPTOR PROTEIN TYROSINE KINASE ACTIVITY | 12 | 64 | 6.754e-06 | 0.0003302 |
20 | DOUBLE STRANDED DNA BINDING | 56 | 764 | 7.181e-06 | 0.0003336 |
21 | MOLECULAR FUNCTION REGULATOR | 86 | 1353 | 8.618e-06 | 0.0003813 |
22 | PROTEIN DOMAIN SPECIFIC BINDING | 48 | 624 | 9.354e-06 | 0.000395 |
23 | GUANYL NUCLEOTIDE EXCHANGE FACTOR ACTIVITY | 29 | 303 | 1.141e-05 | 0.0004489 |
24 | TRANSCRIPTIONAL ACTIVATOR ACTIVITY RNA POLYMERASE II CORE PROMOTER PROXIMAL REGION SEQUENCE SPECIFIC BINDING | 24 | 226 | 1.16e-05 | 0.0004489 |
25 | RAS GUANYL NUCLEOTIDE EXCHANGE FACTOR ACTIVITY | 24 | 228 | 1.345e-05 | 0.0004999 |
26 | TRANSMEMBRANE RECEPTOR PROTEIN KINASE ACTIVITY | 13 | 81 | 1.663e-05 | 0.0005941 |
27 | SMAD BINDING | 12 | 72 | 2.364e-05 | 0.0007947 |
28 | ADENYL NUCLEOTIDE BINDING | 92 | 1514 | 2.395e-05 | 0.0007947 |
29 | TRANSCRIPTION COFACTOR BINDING | 7 | 24 | 2.851e-05 | 0.0009133 |
30 | GTPASE BINDING | 27 | 295 | 4.958e-05 | 0.001535 |
31 | CHROMATIN BINDING | 35 | 435 | 6.153e-05 | 0.001786 |
32 | RNA POLYMERASE II TRANSCRIPTION FACTOR BINDING | 14 | 104 | 6.067e-05 | 0.001786 |
33 | RNA POLYMERASE II ACTIVATING TRANSCRIPTION FACTOR BINDING | 8 | 36 | 6.588e-05 | 0.001855 |
34 | PHOSPHATASE BINDING | 18 | 162 | 7.799e-05 | 0.002128 |
35 | CORE PROMOTER PROXIMAL REGION DNA BINDING | 31 | 371 | 8.019e-05 | 0.002128 |
36 | PROTEIN COMPLEX BINDING | 61 | 935 | 9.076e-05 | 0.002342 |
37 | RIBONUCLEOTIDE BINDING | 105 | 1860 | 0.0001221 | 0.003067 |
38 | TRANSCRIPTION FACTOR ACTIVITY PROTEIN BINDING | 42 | 588 | 0.0001754 | 0.004288 |
39 | PROTEIN KINASE A BINDING | 8 | 42 | 0.0002083 | 0.004962 |
40 | TUBULIN BINDING | 24 | 273 | 0.0002349 | 0.005456 |
41 | CALCIUM ION BINDING | 47 | 697 | 0.0002786 | 0.006312 |
42 | UBIQUITIN LIKE PROTEIN LIGASE BINDING | 23 | 264 | 0.0003575 | 0.007907 |
Num | GO | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|
1 | CELL JUNCTION | 105 | 1151 | 6.163e-16 | 3.599e-13 |
2 | CYTOSKELETON | 146 | 1967 | 3.389e-14 | 9.897e-12 |
3 | ANCHORING JUNCTION | 53 | 489 | 3.179e-11 | 5.4e-09 |
4 | MEMBRANE REGION | 92 | 1134 | 3.699e-11 | 5.4e-09 |
5 | ACTIN CYTOSKELETON | 49 | 444 | 9.563e-11 | 1.117e-08 |
6 | CELL PROJECTION | 125 | 1786 | 1.711e-10 | 1.666e-08 |
7 | SYNAPSE | 66 | 754 | 1.312e-09 | 1.094e-07 |
8 | PLASMA MEMBRANE REGION | 76 | 929 | 1.499e-09 | 1.094e-07 |
9 | CELL LEADING EDGE | 40 | 350 | 1.888e-09 | 1.225e-07 |
10 | CELL SUBSTRATE JUNCTION | 43 | 398 | 2.639e-09 | 1.472e-07 |
11 | NEURON PROJECTION | 76 | 942 | 2.772e-09 | 1.472e-07 |
12 | CYTOSKELETAL PART | 102 | 1436 | 4.936e-09 | 2.402e-07 |
13 | POSTSYNAPSE | 39 | 378 | 5.121e-08 | 2.3e-06 |
14 | SYNAPSE PART | 53 | 610 | 7.508e-08 | 3.132e-06 |
15 | CYTOPLASMIC REGION | 32 | 287 | 1.401e-07 | 5.456e-06 |
16 | CELL CELL JUNCTION | 38 | 383 | 2.09e-07 | 7.628e-06 |
17 | EXCITATORY SYNAPSE | 25 | 197 | 2.869e-07 | 9.855e-06 |
18 | NEURON PART | 87 | 1265 | 3.089e-07 | 1.002e-05 |
19 | MICROTUBULE CYTOSKELETON | 76 | 1068 | 5.013e-07 | 1.541e-05 |
20 | CELL CORTEX | 27 | 238 | 9.364e-07 | 2.734e-05 |
21 | CELL CORTEX PART | 18 | 119 | 1.021e-06 | 2.8e-05 |
22 | CONTRACTILE FIBER | 25 | 211 | 1.055e-06 | 2.8e-05 |
23 | LAMELLIPODIUM | 22 | 172 | 1.283e-06 | 3.257e-05 |
24 | CORTICAL ACTIN CYTOSKELETON | 12 | 58 | 2.28e-06 | 5.549e-05 |
25 | SOMATODENDRITIC COMPARTMENT | 51 | 650 | 2.809e-06 | 6.562e-05 |
26 | APICAL JUNCTION COMPLEX | 18 | 128 | 3.003e-06 | 6.745e-05 |
27 | MEMBRANE MICRODOMAIN | 29 | 288 | 4.261e-06 | 9.215e-05 |
28 | DENDRITE | 39 | 451 | 4.504e-06 | 9.393e-05 |
29 | CELL PROJECTION PART | 65 | 946 | 1.089e-05 | 0.0002192 |
30 | MAIN AXON | 11 | 58 | 1.454e-05 | 0.000283 |
31 | SYNAPTIC MEMBRANE | 26 | 261 | 1.596e-05 | 0.0003006 |
32 | I BAND | 16 | 121 | 2.316e-05 | 0.0004227 |
33 | MICROTUBULE | 34 | 405 | 3.35e-05 | 0.0005929 |
34 | COSTAMERE | 6 | 19 | 6.592e-05 | 0.001132 |
35 | CORTICAL CYTOSKELETON | 12 | 81 | 7.858e-05 | 0.001311 |
36 | SARCOPLASMIC RETICULUM MEMBRANE | 8 | 38 | 9.926e-05 | 0.00161 |
37 | GLYCOPROTEIN COMPLEX | 6 | 21 | 0.0001232 | 0.001944 |
38 | MICROTUBULE ORGANIZING CENTER | 44 | 623 | 0.0001593 | 0.002448 |
39 | CELL CELL CONTACT ZONE | 10 | 64 | 0.0001954 | 0.002926 |
40 | NODE OF RANVIER | 5 | 15 | 0.0002073 | 0.003026 |
41 | CELL CELL ADHERENS JUNCTION | 9 | 54 | 0.0002456 | 0.003498 |
42 | AXON | 32 | 418 | 0.0003075 | 0.004261 |
43 | A BAND | 7 | 34 | 0.0003137 | 0.004261 |
44 | FILOPODIUM | 12 | 94 | 0.000332 | 0.004309 |
45 | SARCOPLASM | 10 | 68 | 0.0003254 | 0.004309 |
46 | PHOSPHATASE COMPLEX | 8 | 48 | 0.0005402 | 0.006712 |
47 | POSTSYNAPTIC MEMBRANE | 19 | 205 | 0.0005325 | 0.006712 |
48 | APICAL PLASMA MEMBRANE | 24 | 292 | 0.0006252 | 0.007606 |
49 | INTERCALATED DISC | 8 | 51 | 0.0008212 | 0.009788 |
Num | Pathway | Pathview | Overlap | Size | P Value | Adj. P Value |
---|---|---|---|---|---|---|
1 | MAPK_signaling_pathway_hsa04010 | 30 | 295 | 2.388e-06 | 7.557e-05 | |
2 | Hippo_signaling_pathway_hsa04390 | 20 | 154 | 3.044e-06 | 7.557e-05 | |
3 | Adherens_junction_hsa04520 | 13 | 72 | 4.36e-06 | 7.557e-05 | |
4 | Rap1_signaling_pathway_hsa04015 | 21 | 206 | 7.304e-05 | 0.0009496 | |
5 | Gap_junction_hsa04540 | 12 | 88 | 0.0001772 | 0.001763 | |
6 | Wnt_signaling_pathway_hsa04310 | 16 | 146 | 0.0002247 | 0.001763 | |
7 | Regulation_of_actin_cytoskeleton_hsa04810 | 20 | 208 | 0.0002373 | 0.001763 | |
8 | Focal_adhesion_hsa04510 | 19 | 199 | 0.0003677 | 0.00239 | |
9 | HIF_1_signaling_pathway_hsa04066 | 12 | 100 | 0.0005886 | 0.003401 | |
10 | PI3K_Akt_signaling_pathway_hsa04151 | 27 | 352 | 0.0008555 | 0.004449 | |
11 | Autophagy_animal_hsa04140 | 13 | 128 | 0.001711 | 0.008087 | |
12 | Calcium_signaling_pathway_hsa04020 | 16 | 182 | 0.002445 | 0.01003 | |
13 | Sphingolipid_signaling_pathway_hsa04071 | 12 | 118 | 0.002508 | 0.01003 | |
14 | Hippo_signaling_pathway_multiple_species_hsa04392 | 5 | 29 | 0.005179 | 0.01747 | |
15 | Ras_signaling_pathway_hsa04014 | 18 | 232 | 0.00521 | 0.01747 | |
16 | Phospholipase_D_signaling_pathway_hsa04072 | 13 | 146 | 0.005376 | 0.01747 | |
17 | Phosphatidylinositol_signaling_system_hsa04070 | 10 | 99 | 0.005833 | 0.01784 | |
18 | ErbB_signaling_pathway_hsa04012 | 9 | 85 | 0.006421 | 0.01855 | |
19 | mTOR_signaling_pathway_hsa04150 | 13 | 151 | 0.007098 | 0.01943 | |
20 | Apelin_signaling_pathway_hsa04371 | 12 | 137 | 0.00831 | 0.02134 | |
21 | AMPK_signaling_pathway_hsa04152 | 11 | 121 | 0.008617 | 0.02134 | |
22 | Hedgehog_signaling_pathway_hsa04340 | 6 | 47 | 0.01019 | 0.02322 | |
23 | Oocyte_meiosis_hsa04114 | 11 | 124 | 0.01027 | 0.02322 | |
24 | cGMP_PKG_signaling_pathway_hsa04022 | 13 | 163 | 0.01302 | 0.02821 | |
25 | FoxO_signaling_pathway_hsa04068 | 11 | 132 | 0.01587 | 0.033 | |
26 | Signaling_pathways_regulating_pluripotency_of_stem_cells_hsa04550 | 11 | 139 | 0.02241 | 0.04483 | |
27 | Cellular_senescence_hsa04218 | 12 | 160 | 0.02555 | 0.04921 | |
28 | Cell_adhesion_molecules_.CAMs._hsa04514 | 11 | 145 | 0.02944 | 0.05468 | |
29 | Tight_junction_hsa04530 | 12 | 170 | 0.03821 | 0.06852 | |
30 | Notch_signaling_pathway_hsa04330 | 5 | 48 | 0.04051 | 0.07022 | |
31 | ECM_receptor_interaction_hsa04512 | 7 | 82 | 0.0437 | 0.07331 | |
32 | TGF_beta_signaling_pathway_hsa04350 | 7 | 84 | 0.04873 | 0.07918 | |
33 | cAMP_signaling_pathway_hsa04024 | 13 | 198 | 0.05185 | 0.08171 | |
34 | Jak_STAT_signaling_pathway_hsa04630 | 11 | 162 | 0.05762 | 0.08614 | |
35 | Cell_cycle_hsa04110 | 9 | 124 | 0.05798 | 0.08614 | |
36 | Endocytosis_hsa04144 | 14 | 244 | 0.1064 | 0.1537 | |
37 | TNF_signaling_pathway_hsa04668 | 7 | 108 | 0.1367 | 0.1922 | |
38 | Apoptosis_multiple_species_hsa04215 | 3 | 33 | 0.141 | 0.193 | |
39 | VEGF_signaling_pathway_hsa04370 | 4 | 59 | 0.2051 | 0.2734 | |
40 | Cytokine_cytokine_receptor_interaction_hsa04060 | 13 | 270 | 0.2743 | 0.3566 | |
41 | Apoptosis_hsa04210 | 7 | 138 | 0.3064 | 0.3886 | |
42 | NF_kappa_B_signaling_pathway_hsa04064 | 5 | 95 | 0.3237 | 0.4007 | |
43 | Necroptosis_hsa04217 | 7 | 164 | 0.4745 | 0.5738 | |
44 | ABC_transporters_hsa02010 | 2 | 45 | 0.5368 | 0.6344 | |
45 | Peroxisome_hsa04146 | 3 | 83 | 0.6437 | 0.7438 | |
46 | Lysosome_hsa04142 | 4 | 123 | 0.7228 | 0.803 | |
47 | p53_signaling_pathway_hsa04115 | 2 | 68 | 0.7568 | 0.8198 | |
48 | Neuroactive_ligand_receptor_interaction_hsa04080 | 7 | 278 | 0.9272 | 0.9462 |