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. 2022 May 18;12:8299. doi: 10.1038/s41598-022-12443-7

Table 1.

List of enriched up/down-regulated pathways.

Group Pathway Fold enrichment P value Genes
Group A Tyrosine metabolism 20.7 8.3E−04 PNMT, MAOA, ADH1B, AOX1
Cytokine-cytokine receptor interaction 3.7 4.0E−02 LEP, CCL3L3, IL1R2, IL18, IFNLR1
Amphetamine addiction 8.2 4.9E−02 GRIA1, MAOA, PPP1R1B
Drug metabolism—cytochrome P450 8.0 5.1E−02 MAOA, ADH1B, AOX1
Neuroactive ligand-receptor interaction  − 5.3 4.0E−03 GRIN2A, GABRA4, TACR1, GRPR, MCHR1, NTSR1
Cytokine-cytokine receptor interaction  − 5.1 1.4E−02 IL1A, CSF2, IL1B, TNFRSF9, CXCR4
Calcium signaling pathway  − 5.5 3.2E−02 GRIN2A, TACR1, GRPR, NTSR1
Salmonella infection  − 8.9 4.2E−02 IL1A, CSF2, IL1B
Hematopoietic cell lineage  − 8.5 4.5E−02 IL1A, CSF2, IL1B
Rheumatoid arthritis  − 8.4 4.6E−02 IL1A, CSF2, IL1B
Group B Drug metabolism—cytochrome P450 15.2 3.6E−05 ADH4, MAOA, ADH1B, ADH1A, AOX1, FMO2
Tyrosine metabolism 24.6 4.1E−05 ADH4, MAOA, ADH1B, ADH1A, AOX1
Retinol metabolism 10.7 5.5E−03 ADH4, ADH1B, ADH1A, AOX1
Fatty acid degradation 12.3 2.3E−02 ADH4, ADH1B, ADH1A
Glycolysis/gluconeogenesis 7.7 5.5E−02 ADH4, ADH1B, ADH1A
Chemical carcinogenesis 6.4 7.5E−02 ADH4, ADH1B, ADH1A
Cell adhesion molecules (CAMs)  − 4.6 8.6E−06 ICAM2, SELE, SELP, HLA-DMB, CDH3, CLDN3, CDH1, PECAM1, HLA-DRA, HLA-DOA, HLA-DQA2, HLA-DQA1, HLA-DRB1, HLA-DQB1
Allograft rejection  − 8.9 1.1E−04 HLA-DMB, HLA-DRA, HLA-DOA, HLA-DQA2, HLA-DRB1, HLA-DQA1, HLA-DQB1
Basal cell carcinoma  − 6.9 1.3E−04 WNT10B, SHH, WNT10A, WNT7B, PTCH2, FZD10, WNT2, WNT4
Type I diabetes mellitus  − 7.8 2.3E−04 HLA-DMB, HLA-DRA, HLA-DOA, HLA-DQA2, HLA-DRB1, HLA-DQA1, HLA-DQB1
Inflammatory bowel disease (IBD)  − 5.8 3.8E−04 HLA-DMB, RORC, HLA-DRA, HLA-DOA, HLA-DQA2, HLA-DRB1, HLA-DQA1, HLA-DQB1
Autoimmune thyroid disease  − 6.3 7.5E−04 HLA-DMB, HLA-DRA, HLA-DOA, HLA-DQA2, HLA-DRB1, HLA-DQA1, HLA-DQB1
Pancreatic secretion  − 4.0 3.5E−03 CPA3, CPB1, FXYD2, KCNQ1, PLA2G2A, CLCA2, CD38, ATP1A2
cAMP signaling pathway  − 2.6 9.2E−03 GRIA2, CHRM1, NPY, FXYD2, PDE3B, CNGA1, ADRB1, ATP1A2, SSTR1, SSTR2, GRIN1
Hippo signaling pathway  − 2.8 1.5E−02 WNT10B, WNT10A, CDH1, WNT7B, RASSF6, FZD10, WNT2, BMP7, WNT4
Wnt signaling pathway  − 2.7 2.7E−02 WNT10B, WNT10A, SFRP2, MMP7, WNT7B, FZD10, WNT2, WNT4
Signaling pathways regulating pluripotency of stem cells  − 2.7 2.9E−02 WNT10B, WNT10A, WNT7B, IGF1, FZD10, WNT2, ISL1, WNT4
Pathways in cancer  − 1.8 3.9E−02 WNT10B, WNT10A, WNT7B, PTCH2, CBLC, KLK3, FZD10, IGF1, MMP9, SHH, GNG4, CDH1, WNT2, NKX3-1, WNT4
cGMP-PKG signaling pathway  − 2.4 5.1E−02 NOS3, FXYD2, PDE2A, PDE3B, CNGA1, ADRB1, ATP1A2, ADRA2A
Adrenergic signaling in cardiomyocytes  − 2.4 7.3E−02 MYL4, TNNT2, FXYD2, KCNQ1, ADRB1, ATP1A2, CACNG4
Cardiac muscle contraction  − 3.1 7.5E−02 MYL4, TNNT2, FXYD2, ATP1A2, CACNG4
Group C Tyrosine metabolism 45.4 2E−3 MAOA, ADH1B, AOX1
Drug metabolism—cytochrome P450 23.3 6E−3 MAOA, ADH1B, AOX1
Tryptophan metabolism 26.5 6.8E−2 MAOA, AOX1
Group D Cytokine-cytokine receptor interaction 4.5 5.1E−2 CCL3L3, IL1R2, IL18, IFNLR1
Neuroactive ligand-receptor interaction  − 5.4 1.1E−2 GRIN2A, GABRA4, TACR1, GRPR, NTSR1
Calcium signaling pathway  − 6.7 1.9E−2 GRIN2A, TACR1, GRPR, NTSR1
Salmonella infection  − 10.8 2.8E−2 IL1A, CSF2, IL1B
Hematopoietic cell lineage  − 10.3 3.1E−2 IL1A, CSF2, IL1B
Rheumatoid arthritis  − 10.2 3.2E−2 IL1A, CSF2, IL1B
Amoebiasis  − 8.5 4.4E−2 CSF2, SERPINB2, IL1B
Measles  − 6.7 6.7E−2 IL1A, IL1B, TACR1
Circadian rhythm  − 19.3 9.5E−2 PER3, NR1D1
Group E Drug metabolism—cytochrome P450 10.5 3.1E−2 ADH4, ADH1A, FMO2
Rap1 signaling pathway 4.5 5.2E−2 FPR1, KDR, FGFR4, RAPGEF5
Cell adhesion molecules (CAMs)  − 4.8 0.000 ICAM2, SELE, SELP, HLA-DMB, CDH3, CLDN3, CDH1, PECAM1, HLA-DRA, HLA-DOA, HLA-DQA2, HLA-DQA1, HLA-DRB1, HLA-DQB1
Type I diabetes mellitus  − 8.2 0.000 HLA-DMB, HLA-DRA, HLA-DOA, HLA-DQA2, HLA-DRB1, HLA-DQA1, HLA-DQB1
Antigen processing and presentation  − 5.2 1E−3 CD74, HLA-DMB, HLA-DRA, HLA-DOA, HLA-DQA2, HLA-DRB1, HLA-DQA1, HLA-DQB1
cAMP signaling pathway  − 2.7 7E-3 GRIA2, CHRM1, NPY, FXYD2, PDE3B, CNGA1, ADRB1, ATP1A2, SSTR1, SSTR2, GRIN1
Proteoglycans in cancer  − 2.7 7E−3 WNT10B, WNT10A, HPSE2, WNT7B, CBLC, IGF1, FZD10, WNT2, HOXD10, MMP9, WNT4
Wnt signaling pathway  − 2.8 2.1E−2 WNT10B, WNT10A, SFRP2, MMP7, WNT7B, FZD10, WNT2, WNT4
Signaling pathways regulating pluripotency of stem cells  − 2.8 2.3E−2 WNT10B, WNT10A, WNT7B, IGF1, FZD10, WNT2, ISL1, WNT4
Pathways in cancer  − 1.9 2.7E−2 WNT10B, WNT10A, WNT7B, PTCH2, CBLC, KLK3, FZD10, IGF1, MMP9, SHH, GNG4, CDH1, WNT2, NKX3-1, WNT4
Phagosome  − 2.6 3.2E−2 HLA-DMB, SFTPA2, HLA-DRA, HLA-DOA, HLA-DQA2, HLA-DRB1, HLA-DQA1, HLA-DQB1
Hippo signaling pathway  − 2.6 3.3E−2 WNT10B, WNT10A, CDH1, WNT7B, FZD10, WNT2, BMP7, WNT4
cGMP-PKG signaling pathway  − 2.5 4.1E−2 NOS3, FXYD2, PDE2A, PDE3B, CNGA1, ADRB1, ATP1A2, ADRA2A
Adrenergic signaling in cardiomyocytes  − 2.5 6E−2 MYL4, TNNT2, FXYD2, KCNQ1, ADRB1, ATP1A2, CACNG4
Cardiac muscle contraction  − 3.3 6.5E−2 MYL4, TNNT2, FXYD2, ATP1A2, CACNG4
Dilated cardiomyopathy  − 2.9 9E−2 DES, TNNT2, ADRB1, IGF1, CACNG4

Group A: DEGs between DEX and ETH treated for short duration (16 h); Group B: DEGs between DEX and ETH treated for longer duration (7 d); Group C: DEGs that overlapping between Group A and Group B; Group D: Uniquely expressed DEGs of HTM cells exposed for 16 h (Group A minus Group C); Group E: Uniquely expressed DEGs of HTM cells exposed for 7 d (Group B minus Group C).