Abstract

BackgroundThe most common primary liver cancer in adults is hepatocellular carcinoma (HCC) which is commonly presented with a poor prognosis. Therefore, it is important to explore effective biomarkers and therapeutic targets for HCC patients. Autophagy is involved in the development and prevention of cancer. Mammalian Beclin-1 is needed for an autophagic vesicle in HCC. Autophagy-related protein-5 (ATG5) is an important molecule involved in cell death during autophagy. The objective is to investigate serum ATG 5 and Beclin 1 levels in HCV-induced liver cirrhosis with and without HCC. The study was conducted on 80 individuals classified into 3 groups:Group 1: 30 patients with HCV-induced liver cirrhosis without HCC.Group 2: 30 patients with HCV-induced liver cirrhosis with HCC.Group 3: 20 healthy subjects (control group).ResultsSerum ATG 5 was significantly lower in HCC than liver cirrhosis patients. Serum Beclin 1 was significantly higher in HCC than liver cirrhosis patients. A cutoff value of < 95.7 and > 5.3 of serum ATG5 and Beclin 1 could be suggested for diagnosis of HCC among patients with HCV-related cirrhosis.ConclusionSerum Beclin 1 and ATG 5 could be used as a novel diagnostic marker for HCC. Moreover, scoring of serum BECLIN 1, ATG 5, and cachexia might be a future promising tool to predict the risk of HCC development.

Highlights

  • The most common primary liver cancer in adults is hepatocellular carcinoma (HCC) which is commonly presented with a poor prognosis

  • All causes of cirrhosis can be complicated by Hepatocellular carcinoma (HCC), but the risk increased in patients with viral hepatitis

  • Increased autophagy flux was detected in advanced cases of HCC and an increased autophagy response was found to be associated with malignant development and poor prognosis of HCC [4, 5]

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Summary

Introduction

The most common primary liver cancer in adults is hepatocellular carcinoma (HCC) which is commonly presented with a poor prognosis. The objective is to investigate serum ATG 5 and Beclin 1 levels in HCV-induced liver cirrhosis with and without HCC. The study was conducted on 80 individuals classified into 3 groups: Group 1: 30 patients with HCV-induced liver cirrhosis without HCC. Group 2: 30 patients with HCV-induced liver cirrhosis with HCC. All causes of cirrhosis can be complicated by HCC, but the risk increased in patients with viral hepatitis. Around one-third of cirrhotic patients will develop HCC during lifetime [2]. Autophagy helps HCC invasion by having effect on the epithelial–mesenchymal transition [6]. It explains why HCC develops in cirrhotic liver rather than in normal liver

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