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Med Oncol ; 29(5): 3055-62, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22653756

ABSTRACT

Progression from chronic hepatitis C virus infection to cirrhosis then to hepatocellular carcinoma usually results in some protein changes in peripheral blood. We evaluated MAGE-4 mRNA, TGFß1 and AFP in peripheral blood as potential biochemical markers for diagnosis and prognosis of some complications of HCV infection. MAGE-4 mRNA in blood by reverse transcription polymerase chain reaction, serum TGF-Β1 and AFP by ELISA was assayed in seventy-five individuals who were classified into five groups: group I (control) comprised fifteen apparently healthy volunteers, group II involved fifteen HCV-infected patients without cirrhosis, group III involved fifteen HCV fifteen HCV-infected patients with cirrhosis, group IV included fifteen HCV-infected patients with cirrhosis and early stage HCC, and group V included fifteen HCV cirrhotic patients and late-stage HCC. We found that the frequency of positivity of MAGE-4 among the late hepatoma group was 40 %, while in the early hepatoma group the positivity was 6.7 %. The results for TGF-Β1 revealed a significant increase in serum TGF-Β1 in groups IV and V as compared to control, II, III groups. The obtained results of AFP showed a significant positive increase in serum AFP in groups IV and V when compared to groups II and III. Detection of MAGE-4 transcripts in blood, especially with follow-up survey, may help to predict the prognosis and monitoring of the response to the therapy, and serum TGF-Β1 level in HCC patients is directly correlated with metastasis and recurrence of tumors and increases gradually with the progression of HCC.


Subject(s)
Antigens, Neoplasm/blood , Biomarkers, Tumor/analysis , Carcinoma, Hepatocellular/blood , Hepatitis C/complications , Liver Neoplasms/blood , Neoplasm Proteins/blood , Transforming Growth Factor beta1/blood , Antigens, Neoplasm/genetics , Biomarkers, Tumor/blood , Biomarkers, Tumor/genetics , Carcinoma, Hepatocellular/genetics , Carcinoma, Hepatocellular/virology , Disease Progression , Enzyme-Linked Immunosorbent Assay , Hepatitis C/blood , Hepatitis C/genetics , Humans , Liver Cirrhosis/blood , Liver Cirrhosis/virology , Liver Neoplasms/genetics , Liver Neoplasms/virology , Neoplasm Proteins/genetics , RNA, Messenger/blood , Reverse Transcriptase Polymerase Chain Reaction , Transforming Growth Factor beta1/analysis
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