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. Author manuscript; available in PMC: 2017 Jun 1.
Published in final edited form as: Diabetologia. 2016 Mar 21;59(6):1297–1306. doi: 10.1007/s00125-016-3913-8

Table 1.

Commonly enriched canonical pathways among the representative shared subnetworks

Pathway description No. of
significant
pathways
Tissue comparison Diabetes comparison
Glom: STZ vs
db/db
SCN: STZ vs
db/db
STZ: SCN vs
Glom
db/db SCN vs
Glom
AKT(PKB)-Bad signalling (EPO signalling pathway (JAK2 STAT1 STAT3 STAT5)) 4 0.010 <0.001 0.020 <0.001
AKT(PKB)-Bad signalling (IL-7 signalling (JAK1 JAK3 STAT5)) 4 0.032 <0.001 0.020 <0.001
Angiopoietin receptor Tie2-mediated signalling 4 <0.001 <0.001 0.004 <0.001
Cytokine receptor degradation signalling (JAK STAT Pathway and Regulation) 4 0.005 <0.001 0.003 0.002
Gene expression (VEGF signalling pathway) 4 0.013 <0.001 0.040 <0.001
IL-6 signalling pathway (JAK1 JAK2 STAT3) 4 0.013 <0.001 0.025 0.032
IL6-mediated signalling events 4 <0.001 <0.001 0.010 0.006
Reelin signalling pathway 4 0.004 0.001 <0.001 <0.001
SHP2 signalling 4 0.013 <0.001 0.003 <0.001
TGFBR 4 0.025 0.004 0.001 <0.001
VEGFR3 signalling in lymphatic endothelium 4 <0.001 <0.001 0.020 0.001
Bioactive peptide-induced signalling pathway 3 0.032 0.013 <0.001
Co-regulation of androgen receptor activity 3 0.032 0.050 0.005
Cyclins and cell cycle regulation 3 <0.001 0.002 0.005
Ephrin B reverse signalling 3 0.032 0.006 0.010
HIF-1-α transcription factor network 3 0.001 0.013 0.002
IGF-1 pathway 3 0.001 0.006 0.016
IGF-1 signalling pathway 3 <0.001 0.050 0.016
Inhibition of cellular proliferation by Gleevec 3 <0.001 0.013 0.025
Integrins in angiogenesis 3 0.013 0.016 0.003
JAK_STAT_MolecularVariation_1 3 0.008 0.020 0.020
JAK_STAT_MolecularVariation_2 3 <0.001 <0.001 0.016
KitReceptor 3 <0.001 0.032 0.016
Regulation of bad phosphorylation 3 0.004 <0.001 0.025
Signalling events mediated by TCPTP 3 0.003 0.016 0.025
Signalling events mediated by VEGFR1 and VEGFR2 3 0.003 0.040 0.006
Syndecan-2-mediated signalling events 3 0.013 0.005 0.020
Syndecan-4-mediated signalling events 3 <0.001 0.002 0.005
IGF-1 receptor and longevity 3 <0.001 0.025 0.001
Validated targets of C-MYC transcriptional repression 3 <0.001 0.005 0.005

The values reported in this table represent the false discovery rate (FDR) for each comparison. No. of significant pathways: the number of comparisons in which the corresponding signalling pathway was significantly over-represented. C-MYC, c-myc avian myelocytomatosis viral oncogene homolog; EPO, erythropoietin; HIF-1-α, hypoxia-inducible factor 1-alpha; SPH2, SH2 domain-containing tyrosine phosphatase; TCPTP, T-cell protein tyrosine phosphatase; TGFBR, transforming growth factor beta receptor; VEGF, vascular endothelial growth factor