TABLE 3.
FDR-q val | ↑ or ↓ | Database | |
WD + vitamin D | |||
CHEMOKINE_SIGNALING_PATHWAY | <0.000 | ↑ | REACTOME |
LEISHMANIA_INFECTION | <0.000 | ↑ | KEGG |
INTERFERON_ALPHA_BETA_SIGNALING | <0.000 | ↑ | REACTOME |
CYTOKINE_CYTOKINE_RECEPTOR_INTERACTION | <0.000 | ↑ | KEGG |
NOD_LIKE_RECEPTOR_SIGNALING_PATHWAY | <0.000 | ↑ | KEGG |
ASTHMA | <0.000 | ↑ | KEGG |
IL12_2PATHWAY | <0.000 | ↑ | PID |
G1_S_TRANSITION | <0.000 | ↑ | REACTOME |
INTEGRIN1_PATHWAY | <0.000 | ↑ | PID |
INTERFERON_GAMMA_SIGNALING | <0.000 | ↑ | REACTOME |
CELL_ADHESION_MOLECULES_CAMS | <0.000 | ↑ | KEGG |
ANTIGEN_PROCESSING_AND_PRESENTATION | <0.001 | ↑ | KEGG |
MITOTIC_G1_G1_S_PHASES | <0.001 | ↑ | REACTOME |
IL23PATHWAY | <0.001 | ↑ | PID |
CHEMOKINE_ACTIVITY | <0.000 | ↑ | GO |
CYTOKINE_ACTIVITY | <0.000 | ↑ | GO |
INFLAMMATORY_RESPONSE | <0.000 | ↑ | GO |
IMMUNE_RESPONSE | <0.000 | ↑ | GO |
EXTRACELLULAR_REGION | <0.001 | ↑ | GO |
REGULATION_OF_CELL_CYCLE | <0.001 | ↑ | GO |
WD + vitamin D + 2 g Ca/d | |||
CHEMOKINE_RECEPTORS_BIND_CHEMOKINES | <0.001 | ↑ | REACTOME |
CHEMOKINE_ACTIVITY | 0.011 | ↑ | GO |
IMMUNE_RESPONSE | 0.049 | ↑ | GO |
PEROXISOME | <0.001 | ↓ | KEGG |
EXCRETION | <0.001 | ↓ | GO |
PEROXISOME | 0.005 | ↓ | GO |
SECRETION | 0.012 | ↓ | GO |
The full list is shown in Supplemental Table 4. The WD was designed as high in fat content (40% of calories) and low in vitamin D (estimated as ∼150–200 IU/d) and calcium (∼400 mg/d). We determined the effects of vitamin D (0.5 μg calcitriol) with or without 2 g supplemental Ca/d on rectosigmoid mucosal gene expression. Note that most of the pathways or processes changed by vitamin D occurred in immune or inflammatory genes with some contribution of cell cycle genes and extracellular matrix protein genes. Most of these effects of vitamin D were abrogated by calcium supplementation. FDR-q val, false discovery rate adjusted significance (q value); WD, Western-style diet; ↑, increase; ↓, decrease.