The mechanism of dysbiosis in alcoholic liver disease leading to liver cancer

• 作者: Alejandro Valencia-Rodríguez Alfonso Vera-Barajas David Q.-H. Wang Emidio Scarpellini Guadalupe Ponciano-Rodríguez Ludovico Abenavoli Nahum Méndez-Sánchez
• 来源期刊: 肝癌研究（英文版）
• 年，卷（期）: 2020,（2）
• 页码范围: 20-32
• 页数: 13页
• 语种: 英文
• DOI: 10.20517/2394-5079.2019.29

摘要

Currently, alcoholic liver disease (ALD) is one of the most prevalent chronic liver diseases worldwide, representing one of the main etiologies of cirrhosis and hepatocellular carcinoma (HCC). Although we do not know the exact mechanisms by which only a selected group of patients with ALD progress to the final stage of HCC, the role of the gut microbiota within the progression to HCC has been intensively studied in recent years. To date, we know that alcohol-induced gut dysbiosis is an important feature of ALD with important repercussions on the severity of this disease. In essence, an increased metabolism of ethanol in the gut induced by an excessive alcohol consumption promotes gut dysfunction and bacterial overgrowth, setting a leaky gut. This causes the translocation of bacteria, endotoxins, and ethanol metabolites across the enterohepatic circulation reaching the liver, where the recognition of the pathogen-associated molecular patterns via specific Toll-like receptors of liver cells will induce the activation of the nuclear factor kappa-B pathway, which releases pro-inflammatory cytokines and chemokines. In addition, the mitogenic activity of hepatocytes will be promoted and cellular apoptosis will be inhibited, resulting in the development of HCC. In this context, it is not surprising that microbiota-regulating drugs have proven effectiveness in prolonging the overall survival of patients with HCC, making attractive the implementation of these drugs as co-adjuvant for HCC treatment.