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. 2019 Apr 15;9:6060. doi: 10.1038/s41598-019-42584-1

Table 1.

Results of microarray studies after IPA analysis.

Ingenuity (IPA) Canonical Pathways Molecules
(A) GD patients vs. controls
Interferon Signalling IFIT3, IFIT1**, OAS1, IFI6, IRF9, STAT1, TAP1, ISG15
Activation of IRF by Cytosolic Pattern Recognition Receptors IFIH1, IRF9, STAT1, IFIT2, ISG15
Protein Ubiquitination Pathway UCHL1, B2M, PSME1, DNAJB4, TAP1, UBE2L6, UCHL3
Oncostatin M Signalling PLAU, STAT1
Coagulation System PLAU, TFPI
Hepatic Fibrosis/Hepatic Stellate Cell Activation LY96, COL4A5, IGFBP5, STAT1
Adipogenesis pathway LPIN1, SMAD9, TXNIP
Parkinson’s Signalling UCHL1
Glioma Invasiveness Signalling RND3, PLAU
VDR/RXR Activation IGFBP5, KLF4
Inhibition of Matrix Metalloproteases THBS2
LXR/RXR Activation LY96, MYLIP
Glucocorticoid Receptor Signalling BCL2L1, PLAU, STAT1
(B) GD patients vs. NPC patients
Interferon Signalling IFIT3,IFIT1,OAS1,MX1,STAT1,TAP1,ISG15
Protein Ubiquitination Pathway PSMA6,DNAJB4,HSPA9,PSME2,TAP1,UCHL3, UCHL1,USO1, HSP90B1,HLA-C,PSMA4,HSPB7, PSMD14,PSMC2,UBE2E1
Activation of IRF by Cytosolic Pattern Recognition Receptors STAT1,NFKB1,IFIT2,ISG15
Glioma Invasiveness Signalling RND3,RHOB,MMP2,PLAU
Oncostatin M Signalling PLAU,STAT1
Coagulation System PROS1,PLAU
IL-17A Signalling in Fibroblasts FOS***, NFKB1
Prostanoid Biosynthesis PTGIS
Glucocorticoid Receptor Signalling FOS,HSP90B1,HSPA9,POLR2H,PLAU,STAT1,NFKB1
Parkinson’s Signalling UCHL1

Cellular canonical pathways with most differentially expressed genes. Comparison ‘GD patients vs. controls’ (part A) and comparison ‘GD patients vs. NPC patients’ (part B)*. *Data were analysed through the use of IPA (QIAGEN Inc., https://www.qiagenbioinformatics.com/products/ingenuity-pathway-analysis).

**Bolded and underlined are genes with most enhanced or inhibited expression after microarray study. *** and 64 other pathways in which FOS was involved, see Supplementary Table S4 part A (all canonical pathways with changed expression).