Background: During the past three decades, the incidence of hepatocellular carcinoma in the United States hastripled. The neuroendocrine character has been observed in some tumor cells within some hepatocellularcarcinoma nodules and elevated serum chromogranin A also been reported in patients with hepatocellularcarcinoma. The aim of this work was to investigate the role of serum concentration of chromogranin A in patientswith hepatocellular carcinoma at different stages.Methods: The study population consisted of 96 patients (63 males and 33 females age range 52-84) at their firsthospital admission for hepatocellular carcinoma. The control group consisted of 35 volunteers (20 males and 15females age range 50-80). The hepatocellular carcinoma patients were stratified according the Barcelona-Clinic LiverCancer classification. Venous blood samples were collected before treatment from each patients before surgery,centrifuged to obtain serum samples and stored at -80° C until assayed.Results: The chromogranin A serum levels were elevated (> 100 ng/ml) in 72/96 patients with hepatocellularcarcinoma. The serum levels of chromogranin A were significantly correlated (p<0.05) with alpha-fetoprotein. Incomparison with controls, the hepatocellular carcinoma patients showed a significant increase (p<0.001) vscontrols. The chromogranin A levels in the Barcelona staging of hepatocellular carcinoma was higher in stage Dcompared to stage C (p<0.01), to stage B (p<0.001), and to stage A (p<0.001).Conclusions: Molecular markers, such as chromogranin A, could be very useful tools for hepatocellular carcinomadiagnosis. However the molecular classification should be incorporated into a staging scheme, which effectivelyseparated patients into groups with homogeneous prognosis and response to treatment, and thus serves to aid inthe selection of appropriate therapy.

Elevated serum levels of Chromogranin A in hepatocellular carcinoma

BIONDI, Antonio Giuseppe;D'AGATA, VELIA MARIA;BASILE, Francesco;DRAGO, Filippo;BERTINO, Gaetano
2012-01-01

Abstract

Background: During the past three decades, the incidence of hepatocellular carcinoma in the United States hastripled. The neuroendocrine character has been observed in some tumor cells within some hepatocellularcarcinoma nodules and elevated serum chromogranin A also been reported in patients with hepatocellularcarcinoma. The aim of this work was to investigate the role of serum concentration of chromogranin A in patientswith hepatocellular carcinoma at different stages.Methods: The study population consisted of 96 patients (63 males and 33 females age range 52-84) at their firsthospital admission for hepatocellular carcinoma. The control group consisted of 35 volunteers (20 males and 15females age range 50-80). The hepatocellular carcinoma patients were stratified according the Barcelona-Clinic LiverCancer classification. Venous blood samples were collected before treatment from each patients before surgery,centrifuged to obtain serum samples and stored at -80° C until assayed.Results: The chromogranin A serum levels were elevated (> 100 ng/ml) in 72/96 patients with hepatocellularcarcinoma. The serum levels of chromogranin A were significantly correlated (p<0.05) with alpha-fetoprotein. Incomparison with controls, the hepatocellular carcinoma patients showed a significant increase (p<0.001) vscontrols. The chromogranin A levels in the Barcelona staging of hepatocellular carcinoma was higher in stage Dcompared to stage C (p<0.01), to stage B (p<0.001), and to stage A (p<0.001).Conclusions: Molecular markers, such as chromogranin A, could be very useful tools for hepatocellular carcinomadiagnosis. However the molecular classification should be incorporated into a staging scheme, which effectivelyseparated patients into groups with homogeneous prognosis and response to treatment, and thus serves to aid inthe selection of appropriate therapy.
2012
Hepatocellular carcinoma; Chromogranin A
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/31569
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