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. 2017 Nov 13;9(11):366. doi: 10.3390/toxins9110366

Table 4.

Comparison of the five most significant canonical pathways altered in bovine macrophage cells (BoMac) after 24 h of exposure to citrinin (CIT), ochratoxin A (OTA) or citrinin + ochratoxin A (CIT/OTA).

Most-Altered Canonical Pathways 1 Ratio 2 p Value 3
Citrinin
Superpathway of cholesterol biosynthesis 17/23 (0.739) ***
Cholesterol biosynthesis I 8/10 (0.80) ***
Cholesterol biosynthesis II (via 24, 25-dihydrolanosterol) 8/10 (0.80) ***
Cholesterol biosynthesis III (via desmosterol) 8/10 (0.80) ***
tRNA charging 16/32 (0.5) ***
Ochratoxin A
P2Y purigenic receptor signaling pathway 43/93 **
Breast cancer regulation by Stathmin1 58/137 **
PPAR signaling 33/69 (0.478) **
CREB signaling in neurons 50/117 (0.427) **
GADD45 Signaling 11/17 (0.647) **
Citrinin + Ochratoxin A
EIF2 signaling 85/182 (0.443) ***
Regulation of eIF4 and p70S6K signaling 57/146 (0.39) ***
Molecular mechanisms of cancer 114/365 (0.312) ***
mTOR signaling 67/188 (0.356) ***
Germ cell-Sertoli cell junction signaling 56/160 (0.35) ***

1 Differentially expressed genes in CIT, OTA and CIT + OTA groups at 6 h after PM exposure underwent Core analysis, which interprets the data set in the context of biological processes, pathways and molecular networks (Ingenuity® Systems); 2 (Differentially expressed genes)/(Total number of genes on the pathway); 3 A p-value associated with a pathway was calculated using Fisher’s exact test to determine the probability that the association between affected genes and a canonical pathway is explained by chance alone; * denotes significance at p < 0.05; ** denotes significance at p < 0.01; *** denotes significance at p < 0.01.