Table 1. Genes and potential biomarkers identified for HCC-CC, HCC, CC and associated conditions.
Conditions | Total genes |
---|---|
HCC-CC | 50 |
HCC | 690 |
HCC pathologic subtypes | |
Fibrolamellar HCC | 5 |
Scirrhous HCC | 2 |
Sarcomatoid HCC | 11 |
Lympho-epithelial-like HCC | 94 |
HCC risk factors | |
Cirrhosis | 352 |
Portal hypertension | 30 |
Infectious | |
Hepatitis C | 272 |
Hepatitis B | 293 |
Toxin | |
Alcoholic fatty liver | 30 |
Aflatoxin | 6 |
Peliosis hepatis | 2 |
Autoimmune | |
Autoimmune hepatitis | 206 |
Primary biliary cirrhosis | 118 |
Granulomatous, hepatitis | 11 |
Metabolic | |
Fatty liver disease | 125 |
Nonalcoholic steatohepatitis | 9 |
Hemochromatosis | 52 |
Glycogen storage diseases | 52 |
Wilson disease | 26 |
Porphyria cutanea tarda | 20 |
Alpha-1, antitrypsin | 20 |
Tyrosinemia | 15 |
Vascular | |
Portal vein thrombosis | 9 |
Budd-Chiari syndrome | 5 |
CC | 98 |
CC pathologic subtypes | |
Intraductal papillary CC | 2 |
Intestinal-type CC | 8 |
Clear cell CC | 12 |
Signet-ring CC | 0 |
Squamous Cell CC | 54 |
Small cell CC | 39 |
CC risk factors | |
Primary sclerosing cholangitis | 41 |
Congenital | |
Cystic disease of liver | 97 |
Biliary cyst | 20 |
Choledochal cyst | 8 |
Caroli disease | 2 |
Other congenital malformations of bile ducts | 1 |
Other congenital malformations of gallbladder | 1 |
Infectious | |
Cholangitis | 58 |
Schistosomiasis | 43 |
Opisthorchiasis | 12 |
Clonorchiasis | 12 |
Recurrent cholangitis | 7 |
Anatomic | |
Biliary stricture | 2 |
HCC-CC, hepatocellular carcinoma-cholangiocarcinoma; HCC, hepatocellular carcinoma; CC, cholangiocarcinoma.