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. Author manuscript; available in PMC: 2019 Apr 1.
Published in final edited form as: Drug Metab Pharmacokinet. 2018 Mar 10;33(2):133–140. doi: 10.1016/j.dmpk.2018.03.003

Table 2.

Significantly altered biological pathways in the Hep3B, HepG2, and Huh7 cell lines compared to human livers.

Hep3B vs HLM HepG2 vs HLM Huh7vs HLM
Pathway name q-value Trend Pathway name q-value Trend Pathway name q-value Trend
Non-alcoholic fatty liver disease 6.0E−03 Chemical carcinogenesis 4.5E−04 Ribosome 5.4E−05
Metabolism of xenobiotics by cytochrome P450 6.0E−03 Metabolism of xenobiotics by cytochrome P450 5.2E−04 Metabolism of xenobiotics by cytochrome P450 2.2E−04
Steroid hormone biosynthesis 7.0E−03 Parkinson’s disease 7.0E−03 Drug metabolism-cytochrome P450 2.0E−03
Alzheimer’s disease 7.0E−03 Alzheimer’s disease 7.0E−03 Alzheimer’s disease 2.0E−03
Spliceosome 9.0E−03 Drug metabolism-cytochrome P450 1.9E−02 Steroid hormone biosynthesis 3.0E−03
Drug metabolism-cytochrome P450 1.2E−02 Metabolic pathways 1.9E−02 Chemical carcinogenesis 5.0E−03
Metabolic pathways 1.3E−02 Biosynthesis of amino acids 1.9E−02 Non-alcoholic fatty liver disease 2.4E−02
Peroxisome 1.5E−02 Non-alcoholic fatty liver disease 1.9E−02 Drug metabolism - other enzymes 2.6E−02
Chemical carcinogenesis 2.7E−02 Spliceosome 2.3E−02 Retinol metabolism 3.8E−02
Parkinson’s disease 2.9E−02 Drug metabolism - other enzymes 3.0E−02 Spliceosome 3.9E−02
Oxidative phosphorylation 3.4E−02 Steroid hormone biosynthesis 3.0E−02 Parkinson’s disease 4.5E−02
mRNA surveillance pathway 4.0E−02