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. 2021 Jan 19;106(5):e2299–e2308. doi: 10.1210/clinem/dgaa964

Table 1.

Significantly enriched pathways in tumor tissue

No Pathway P-value FDR P-value
1 Cell adhesion_ECM remodeling 2.76–07 0.0001247
2 Cell adhesion_Chemokines and adhesion 1.06–05 0.0024
3 Immune response_Antigen presentation by MHC class II 4.31–05 0.006169
4 Cell adhesion_Endothelial cell contacts by non-junctional mechanisms 5.47-05 0.006169
5 Cell adhesion_Integrin-mediated cell adhesion and migration 1.93–04 0.01743
6 LRRK2 in neurons in Parkinson’s disease 2.68–04 0.02018
7 Cell adhesion_Plasmin signaling 3.57–04 0.02275
8 Development_Hedgehog and PTH signaling pathways in bone and cartilage development 4.08-04 0.02275
9 Cytoskeleton remodeling_Cytoskeleton remodeling 4.54-04 0.02275
10 Transport_Macropinocytosis regulation by growth factors 8.59-04 0.03225
11 Development_Leptin signaling via JAK/STAT and MAPK cascades 9.20-04 0.03225
12 Development_Regulation of epithelial-to-mesenchymal transition (EMT) 9.34-04 0.03225
13 Cell adhesion_Cadherin-mediated cell adhesion 1.07–03 0.03225
14 Immune response_IL-10 signaling pathway 1.07–03 0.03225
15 Development_S1P2 and S1P3 receptors in cell proliferation and differentiation 1.07–03 0.03225
16 Regulation of degradation of deltaF508 CFTR in CF 1.24–03 0.035
17 Development_Slit-Robo signaling 1.86–03 0.04935

Table shows significantly enriched pathways (FDR P-value < 0.05) in tumor tissue based on identified differentially expressed genes. Common up- and downregulated genes were identified upon comparing tumor tissue to both adjacent and skin tissue. Pathway names, raw P-value, and FDR P-value are given.