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. 2016 Aug;7(4):570–579. doi: 10.21037/jgo.2016.04.01

Table S3. Genes and potential biomarkers present for each risk factor for HCC-CC.

Gene function Gene name General Infectious Metabolic Congenital Autoimmune Carcinogen Vascular
Cirrhosis PHTN Hepatitis C Hepatitis B Cholangitis Opisthorchiasis Recurrent cholangitis NAFLD NASH Tyrosinemia Cystic disease of liver Biliary cyst Choledochal cyst Other congenital malformations of gallbladder AIH PBC PSC Alcoholic fatty liver Alcohol Aflatoxin PVT
Embryonic AFP F
CEACAM3
GPC3
Hormonal CCKBR
SCT
Cell Adhesion HGF
MET
Cytokeratin KRT7
KRT8
KRT18
KRT19
Mucin Production MUC2
MUC5AC
Metalloproteins MME
MMP7
RECK
TIMP3
Ras Signaling KRAS
RAF1
RASSF1
Metabolism ALPL
ALPP
ALPPL2
CHKA
GGT1
NAT2
PTGS2
Apoptosis MCL1
PIK3CA
TERT

HCC-CC, hepatocellular carcinoma-cholangiocarcinoma; HCC, hepatocellular carcinoma; CC, cholangiocarcinoma; ECM, extracellular membrane; ER, endoplasmic reticulum; MMP, matrix metalloproteinase, GTPase, guanyl triphosphatase; COX, cyclo-oxygenase; BCL-2, B-cell lymphoma 2; ATP, adenosine tri-phosphate; PHTN, portal hypertension; NAFLD, non-alcoholic fatty liver disease; NASH, non-alcoholic steatohepatitis; AIH, autoimmune hepatitis; PBC, primary biliary cirrhosis; PSC, primary sclerosing cholangitis; PVT, portal vein thrombosis.