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. 2019 Oct 15;10:1200. doi: 10.3389/fphar.2019.01200

Table 2.

Significant pathways with related pathogenic genes and predicted genes.

Significant Pathways 20 Pathogenic Genes and 18 Interacted Genes P value
Epithelial to mesenchymal transition in colorectal cancer COL4A6, WNT8B, SPARC, WNT1 0.00083567
Focal Adhesion-PI3K-Akt-mTOR-signaling pathway COL4A6, COL5A2, COL1A1, COL1A2, CREB3L1 0.0010862
miR-509-3p alteration of YAP1/ECM axis COL1A1, SPARC 0.0011611
Focal Adhesion COL4A6, COL5A2, COL1A1, COL1A2 0.0018166
Inflammatory Response Pathway COL1A1, COL1A2 0.0035058
miRNA targets in ECM and membrane receptors COL5A2, COL1A2 0.0059006
PI3K-Akt Signaling Pathway COL4A6, COL1A1, COL1A2, CREB3L1 0.012283
Sterol Regulatory Element-Binding Proteins (SREBP) signaling MBTPS2, SEC24D 0.01637
Hypothetical Craniofacial Development Pathway WNT1 0.021586
ncRNAs involved in Wnt signaling in hepatocellular carcinoma SERPINF1, WNT1 0.023282
LncRNA involvement in canonical Wnt signaling and colorectal cancer SERPINF1, WNT1 0.031757
Senescence and Autophagy in Cancer COL1A1, SPARC 0.034042
EDA Signaling in Hair Follicle Development BMP1 0.037488
Osteoblast Signaling COL1A1 0.037488
Wnt Signaling Pathway SERPINF1, WNT1 0.040029
Canonical and Non-Canonical TGF-B signaling BMP1 0.045347
Regulation of Wnt/B-catenin Signaling by Small Molecule Compounds WNT1 0.047953
Adipogenesis BMP1, WNT1 0.04837

Eighteen significant pathways (P < 0.05) were identified with 20 OI causative genes and their 18 interacting gene partners from protein–protein interaction network. Candidate genes (the predicted gene set B) are represented in bold font.