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. 2019 Jan 11;10(4):480–493. doi: 10.18632/oncotarget.26558

Table 1. Ontology for biological processes represented in the top 300 enriched proteins identified in post-IACC samples.

Biological Process REFLIST Protein Hits Expected Fold Enrichment Raw P-value FDR
MAPK cascade (GO:0000165) 340 34 5.36 6.34 1.15E-16 2.81E-14
intracellular signal transduction (GO:0035556) 1071 53 16.9 3.14 4.26E-13 5.20E-11
signal transduction (GO:0007165) 2318 83 36.57 2.27 1.91E-12 1.55E-10
cell surface receptor signaling pathway (GO:0007166) 1206 55 19.03 2.89 3.22E-12 1.97E-10
developmental process (GO:0032502) 1501 62 23.68 2.62 6.31E-12 3.08E-10
response to stimulus (GO:0050896) 2677 87 42.24 2.06 5.37E-11 2.19E-09
negative regulation of apoptotic process (GO:0043066) 99 15 1.56 9.6 2.81E-10 9.79E-09
regulation of catalytic activity (GO:0050790) 359 26 5.66 4.59 4.05E-10 1.24E-08
cell communication (GO:0007154) 2686 85 42.38 2.01 5.07E-10 1.38E-08
transmembrane receptor PTK signaling pathway (GO:0007169) 151 17 2.38 7.14 1.17E-09 2.86E-08
regulation of phosphate metabolic process (GO:0019220) 537 30 8.47 3.54 5.81E-09 1.18E-07
regulation of molecular function (GO:0065009) 441 27 6.96 3.88 5.69E-09 1.26E-07
immune system process (GO:0002376) 669 33 10.56 3.13 1.76E-08 3.31E-07
apoptotic process (GO:0006915) 336 22 5.3 4.15 5.09E-08 8.87E-07
immune response (GO:0006955) 383 23 6.04 3.81 1.10E-07 1.79E-06
cell death (GO:0008219) 356 22 5.62 3.92 1.32E-07 1.89E-06
death (GO:0016265) 356 22 5.62 3.92 1.32E-07 2.01E-06
cell differentiation (GO:0030154) 548 25 8.65 2.89 3.86E-06 4.70E-05
biological regulation (GO:0065007) 2985 79 47.1 1.68 3.82E-06 4.90E-05
locomotion (GO:0040011) 310 18 4.89 3.68 4.24E-06 4.92E-05
response to external stimulus (GO:0009605) 351 19 5.54 3.43 5.99E-06 6.64E-05
regulation of biological process (GO:0050789) 2463 67 38.86 1.72 1.05E-05 1.07E-04
cytokine-mediated signaling pathway (GO:0019221) 60 8 0.95 8.45 1.02E-05 1.09E-04
biological adhesion (GO:0022610) 356 16 5.62 2.85 2.55E-04 2.31E-03
cell adhesion (GO:0007155) 356 16 5.62 2.85 2.55E-04 2.40E-03
angiogenesis (GO:0001525) 18 4 0.28 14.08 3.35E-04 2.82E-03
cellular component movement (GO:0006928) 480 19 7.57 2.51 3.27E-04 2.85E-03
protein phosphorylation (GO:0006468) 81 7 1.28 5.48 4.43E-04 3.60E-03
cell-cell adhesion (GO:0016337) 141 9 2.22 4.05 5.77E-04 4.40E-03
protein folding (GO:0006457) 94 7 1.48 4.72 1.01E-03 7.48E-03
response to stress (GO:0006950) 653 22 10.3 2.14 1.19E-03 8.32E-03
proteolysis (GO:0006508) 448 17 7.07 2.41 1.68E-03 1.11E-02
cell-matrix adhesion (GO:0007160) 51 5 0.8 6.21 1.75E-03 1.13E-02
cellular calcium ion homeostasis (GO:0006874) 115 7 1.81 3.86 2.99E-03 1.82E-02
response to interferon-gamma (GO:0034341) 58 5 0.92 5.46 2.95E-03 1.85E-02
cellular process (GO:0009987) 8247 157 130.12 1.21 3.19E-03 1.90E-02
behavior (GO:0007610) 61 5 0.96 5.2 3.61E-03 2.10E-02
induction of apoptosis (GO:0006917) 41 4 0.65 6.18 5.16E-03 2.86E-02
ectoderm development (GO:0007398) 212 9 3.34 2.69 7.90E-03 4.10E-02

To analyse our proteomic data, we used Gene PANTHER (Protein ANnotation THrough Evolutionary Relationships) classification system (http://www.pantherdb.org/) that combines gene function, ontology, pathways and statistical analysis tools to analyze large-scale, genome-wide data from proteomics experiments. The False Discovery Rate (FDR) adjusts the value at which a test is considered “significant” based on the rank of the predicted level of significance.