Detailed information |
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CancerLivER ID | 2506 |
Biomarker | Zinc finger protein, integrin alpha 6, hepatoma derived growth factor, TGF beta induced, Macrophage inhibitory cytokine 1, lymphocyte antigen, aldehyde oxidase, c-myc purine binding transcription factor puf, plasminogen, vitronectin, hemoglobin alpha subunit, cytosolic superoxide dismutase, methylen |
Biomarker Name/Symbol (given in Publication) | Zinc finger protein, integrin alpha 6, hepatoma derived growth factor, TGF beta induced, Macrophage inhibitory cytokine 1, lymphocyte antigen, aldehyde oxidase, c-myc purine binding transcription factor puf, plasminogen, vitronectin, hemoglobin alpha subunit, cytosolic superoxide dismutase, methylenetetrahydrofolate dehydrogease, Dihydro-orotate dehydrogenas |
Biomolecule | RNAs |
Subject | Human |
Degree of Validity | Potential diagnostic marker for HCC and diffrenetially expressed in moderately differentiated HCC v/s poorly differentiated HCC; but not validated on independent dataset |
Experimental Condition | moderately differentiated HCC v/s poorly differentiated HCC |
Cancer type | Hepatocellular carcinoma |
Regulation | Diffrenetially expressed in moderately differentiated HCC v/s poorly differentiated HCC |
Level of significance | p < 0.01 |
Source | Tissue |
PMID | 11973655 |
Type of Biomarker | Diagnostic |
Pathway | Metabolic pathways, growth factor, regulate immune response, cell cycle, cytoskelton |
Cohort | 15 HCC patients: 8 HCV positive-HCC, 6 HBV-positive HCC and one HCV and HBV associated HCC. Histological analysis of non-tumour tissues showed that 11 HCCs had developed on cirrhotic and 4 on non-cirrhotic tissues; 5 well differentiated HCCs, and 10 moderately or poorly differentiated HCC. |
Sensitivity | NA |
Specificity | NA |
Accuracy | NA |
AUC | NA |
Disease | moderately differentiated HCC v/s poorly differentiated HCC |
Year of Publication | 2002 |
Clinical trial | NO |
Clinical trial (NCT Number) | NA |