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. 2016 May 11;6:25619. doi: 10.1038/srep25619

Table 4. Top 15 Ingenuity Canonical Pathways predicted to be enriched (p < 0.05) based on the integrated “verified” dataset.

# Ingenuity Canonical Pathways Molecules Rank, Cell extract Rank, ER/Golgi Rank, CM Rank, Glad4U Rank, BCCluster
1 Interferon Signaling IFIT1, STAT1, IFIT3, ISG15, MX1, IFI35, BAX 5 3 Not predicted 303 272
2 Superoxide Radicals Degradation SOD2, SOD3, CAT, NQO1 34 92 (n.s.) 8 313 Not predicted
3 Caveolar-mediated Endocytosis Signaling HLA-A, ITGAV, DNM2, ITGB1, ITGA6, B2M, HLA-B, FLOT2 28 5 20 282 233
4 Hepatic Fibrosis / Hepatic Stellate Cell Activation NFKB2, IGFBP4, COL12A1, STAT1, CSF1, BAX, IL6, ICAM1, VEGFC, COL18A1, CXCL8, MYH9 200 (n.s.) 197 (n.s.) 2 4 8
5 Role of Tissue Factor in Cancer ITGAV, ITGB1, CSF1, ITGA6, CXCL1, YES1, VEGFC, CXCL8, ARRB1 100 (n.s.) 19 34 27 15
6 Role of IL-17F in Allergic Inflammatory Airway Diseases NFKB2, CXCL6, CXCL10, CXCL1, IL6, CXCL8 275 (n.s.) Not predicted 11 120 242
7 Putrescine Degradation III ALDH3A2, IL4I1, ALDH3A1, ALDH1A3 19 45 149 (n.s.) 348 (n.s.) 336 (n.s.)
8 Tryptophan Degradation X (Mammalian, via Tryptamine) ALDH3A2, IL4I1, ALDH3A1, ALDH1A3 21 47 154 (n.s.) 351 (n.s.) 340 (n.s.)
9 Ethanol Degradation IV ALDH3A2, CAT, ALDH3A1, ALDH1A3 6 52 Not predicted 357 (n.s.) 420 (n.s.)
10 Complement System CFB, C3, C1QBP, C1S, C1R Not predicted 195 (n.s.) 3 Not predicted 339 (n.s.)
11 Dopamine Degradation ALDH3A2, IL4I1, ALDH3A1, ALDH1A3 27 59 168 (n.s.) 320 362 (n.s.)
12 IL-8 Signaling ITGAV, PLD3, CXCL1, GNG12, BAX, LASP1, RAC2, ICAM1, VEGFC, CXCL8 75 17 62 8 4
13 Virus Entry via Endocytic Pathways HLA-A, DNM2, ITGB1, ITGA6, B2M, HLA-B, RAC2 72 4 24 213 99
14 Role of Pattern Recognition Receptors in Recognition of Bacteria and Viruses EIF2AK2, NFKB2, C3, OAS3, OAS2, DDX58, IL6, CXCL8 59 128 (n.s.) 23 55 166
15 Pentose Phosphate Pathway TKT, G6PD, PGLS 8 26 26 380 (n.s.) 391 (n.s.)

Pathways were ranked based on the significance level. Subsequently, the overlap between the top 15 pathways, as defined based on the integrated “verified” dataset, and pathways predicted based on the individual proteomics datasets (CE, ER/Golgi, CM) and literature mined dataset was established. The respective rank for the overlapping pathways is indicated. Significant pathways with the rank ≤ 15 are marked in bold, while significant pathways with rank > 15 are marked in italics. (n.s. not significant results).