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Table 1 A total of 10 hub genes screened by MCC, MNC and Degree methods, and showed the functions by literature search

From: Comparative analysis of gene expression between mice and humans in acetaminophen-induced liver injury by integrating bioinformatics analysis

Name

Express by bioinformatics analysis

Function

CYP7A1

down

Catalyze a rate-limiting step in cholesterol catabolism and bile acid biosynthesis [29].

LSS

down

Synthesize lanosterol in the key cyclization reaction of l cholesterol biosynthesis and associated with glutathione peroxidase activity (Gpx) levels [30].

SREBF1

down

Regulate transcription of the LDL receptor gene as well as the fatty acid and to a lesser degree the cholesterol synthesis pathway [31].

FASN

down

Catalyze the formation of long- chain fatty acids from acetyl-CoA, malonyl-CoA and NADPH [32].

CD44

up

The Chi3l1/CD44 axis as a critical pathway mediating APAP-induced hepatic platelet recruitment and tissue injury [33].

SPP1

up

Characterize bile duct–associated macrophages and correlates with liver fibrosis severity [35, 36].

ITGAV

up

Play a central role in the progression of liver fibrosis as a known profibrogenic cytokine [38].

ANXA5

up

Regulate hepatic macrophage polarization [34].

LGALS3

up

Act as a mediator of acute inflammatory responses, including neutrophil activation and adhesion, monocyte macrophage hemoattraction, etc. [37].

PDGFRA

up

Play an essential role in the regulation of embryonic development, cell proliferation, survival and chemotaxis [39].