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. 2021 Jul 12;53(8):358–371. doi: 10.1152/physiolgenomics.00001.2021

Table 3.

Canonical pathways affected by OVX and OVX in the context of CBA

Ingenuity Canonical Pathway P Value of Overlap Ratio
OVX effects
Acute phase response signaling 6.57E-13 13/179
LXR/RXR activation* 2.23E-09 9/121
FXR/RXR activation* 3.19E-09 9/126
Clathrin-mediated endocytosis signaling* 1.30E-07 9/193
Coagulation system 3.55E-07 5/35
Atherosclerosis signaling 1.66E-05 6/127
Neuroprotective role of THOP1 in Alzheimer’s disease 1.34E-04 5/116
Production of nitric oxide and reactive oxygen species in macrophages 1.48E-04 6/188
IL-12 signaling and production in macrophages 2.45E-04 5/132
Intrinsic prothrombin activation pathway 7.43E-04 3/42
Sirtuin signaling pathway* 1.48E-03 6/291
Extrinsic prothrombin activation pathway 2.04E-03 2/16
Caveolar-mediated endocytosis signaling 3.66E-03 3/73
Macropinocytosis signaling 4.10E-03 3/76
Acetyl-CoA biosynthesis III (from Citrate)* 4.22E-03 1/1
Apelin liver signaling pathway 5.37E-03 2/26
Xenobiotic metabolism AHR signaling pathway* 5.61E-03 3/85
Palmitate biosynthesis I (animals)* 8.43E-03 1/2
Fatty acid biosynthesis Initiation II* 8.43E-03 1/2
PPARα/RXRα activation* 8.64E-03 4/190
Xenobiotic metabolism PXR signaling pathway 8.95E-03 4/192
OVX in the context of CBA
Mitochondrial dysfunction 1.05E-12 13/171
Oxidative phosphorylation 7.55E-11 10/109
Sirtuin signaling pathway* 8.18E-10 13/291
Glutaryl-CoA degradation 7.21E-07 4/16
Valine degradation I 1.52E-06 4/19
Tryptophan degradation III (eukaryotic) 3.42E-06 4/23
Ketolysis 1.09E-05 3/10
Fatty acid β-oxidation I 1.35E-05 4/32
Ketogenesis 1.49E-05 3/11
LXR/RXR activation* 1.99E-05 6/121
Mevalonate pathway I 3.26E-05 3/14
Isoleucine degradation I 4.99E-05 3/16
Biotin-carboxyl carrier protein assembly 6.20E-05 2/3
Stearate biosynthesis I (animals) 6.88E-05 4/48
Superpathway of geranylgeranyldiphosphate biosynthesis I (via mevalonate) 7.22E-05 3/18
TCA cycle II (eukaryotic) 1.75E-04 3/24
NRF2-mediated oxidative stress response 2.35E-04 6/189
Superpathway of cholesterol biosynthesis 3.12E-04 3/29
Ethanol degradation II 4.19E-04 3/32
Iron homeostasis signaling pathway 4.21E-04 5/137
Acetyl-CoA biosynthesis I (pyruvate dehydrogenase complex) 4.29E-04 2/7
AMPK signaling 4.57E-04 6/214
Noradrenaline and adrenaline degradation 5.47E-04 3/35
Superoxide radicals degradation 5.70E-04 2/8
Xenobiotic metabolism AHR signaling pathway* 6.29E-04 4/85
Sucrose degradation V (mammalian) 7.31E-04 2/9
Folate transformations I 7.31E-04 2/9
Glycine betaine degradation 9.10E-04 2/10
Acyl-CoA hydrolysis 1.56E-03 2/13
PPARα/RXRα activation* 1.82E-03 5/190
Clathrin-mediated endocytosis signaling* 1.95E-03 5/193
FXR/RXR activation* 2.70E-03 4/126
Serotonin degradation 3.60E-03 3/67
LPS/IL-1 mediated inhibition of RXR function 3.71E-03 5/224
Aryl hydrocarbon receptor signaling 4.24E-03 4/143
Acetyl-CoA biosynthesis III (from citrate)* 4.57E-03 1/1
Glycolysis I 6.27E-03 2/26
Gluconeogenesis I 6.27E-03 2/26
Palmitate biosynthesis I (animals)* 9.13E-03 1/2
Fatty acid biosynthesis initiation II* 9.13E-03 1/2
Glycine biosynthesis I 9.13E-03 1/2

Ratio is the number of differentially expressed proteins in our data set that were implicated in the pathway relative to the total number of proteins in that pathway. AHR, aryl hydrocarbon receptor; AMPK, adenosine monophosphate-activated protein kinase; CBA, chronic binge alcohol; FXR, farnesoid X receptor; LXR, liver X receptor; OVX, ovariectomy; PPARα, peroxisome proliferator-activated receptor alpha; RXR, retinoid X receptor. Only pathways with P value of overlap 10−3 are shown. *Pathways that are enriched in both comparisons.