Yadav Satyam, Kumar Ranjeet
ISF College of Pharmacy, Department of Pharmacy Practice, Moga, Punjab, India.
Narayan Institute of Pharmacy, Gopal Narayan Singh University, Sasaram, Rohtas, Bihar, 821305, India.
Anticancer Agents Med Chem. 2025 Mar 13. doi: 10.2174/0118715206364200250304034753.
Hepatocellular carcinoma (HCC) is among the most prevalent and fatal cancers globally. The gut-liver axis, involving intricate interactions between gut microbiota and the liver, has emerged as a critical pathway in HCC development. This review comprehensively examines the molecular mechanisms by which gut microbiota contribute to hepatocarcinogenesis. It discusses factors that either protect against or promote HCC, such as bacterial translocation, and explores the biological processes that drive carcinogenesis, while addressing clinical and pathophysiological complexities. Special attention is given to the role of toll-like receptors (TLRs) and inflammation in liver cells, where microbial components trigger changes in TLR activation, leading to increased inflammation and fibrosis. Additionally, the review covers obesity-related HCC, highlighting the impact of gut microbiota alterations on this cancer type. It critically assesses current literature on therapeutic interventions targeting gut microbiota in HCC, focusing on strategies like probiotics and antibiotics that could modulate microbial composition to prevent HCC progression. The review also explores gut microbiota-derived biomarkers for early detection and monitoring of HCC and discusses personalized therapies based on individual gut-liver interactions. Finally, it identifies research gaps and suggests future studies to deepen understanding of how gut microbiota can be leveraged as an adjunct therapy in HCC. Overall, the review underscores the pivotal role of gut microbiota in HCC pathogenesis and treatment, pointing to microbiome modulation as a promising therapeutic avenue.
肝细胞癌(HCC)是全球最常见且致命的癌症之一。肠道-肝脏轴涉及肠道微生物群与肝脏之间复杂的相互作用,已成为HCC发展的关键途径。本综述全面研究了肠道微生物群促成肝癌发生的分子机制。它讨论了诸如细菌易位等预防或促进HCC的因素,并探讨了驱动致癌作用的生物学过程,同时阐述了临床和病理生理复杂性。特别关注了Toll样受体(TLR)和炎症在肝细胞中的作用,其中微生物成分会引发TLR激活的变化,导致炎症和纤维化增加。此外,该综述涵盖了与肥胖相关的HCC,强调了肠道微生物群改变对这种癌症类型的影响。它批判性地评估了目前关于针对HCC肠道微生物群的治疗干预措施的文献,重点关注益生菌和抗生素等可调节微生物组成以预防HCC进展的策略。该综述还探索了用于早期检测和监测HCC的肠道微生物群衍生生物标志物,并讨论了基于个体肠道-肝脏相互作用的个性化疗法。最后,它确定了研究差距,并建议开展未来研究以加深对如何将肠道微生物群用作HCC辅助治疗的理解。总体而言,该综述强调了肠道微生物群在HCC发病机制和治疗中的关键作用,指出微生物群调节是一条有前景的治疗途径。