From Liver Cirrhosis to Cancer: The Role of Micro-RNAs in Hepatocarcinogenesis

Int J Mol Sci. 2021 Feb 2;22(3):1492. doi: 10.3390/ijms22031492.

Abstract

In almost all cases, hepatocellular carcinoma (HCC) develops as the endpoint of a sequence that starts with chronic liver injury, progresses to liver cirrhosis, and finally, over years and decades, results in liver cancer. Recently, the role of non-coding RNA such as microRNA (miRNA) has been demonstrated in the context of chronic liver diseases and HCC. Moreover, data from a phase II trial suggested a potential role of microRNAs as therapeutics in hepatitis-C-virus infection, representing a significant risk factor for development of liver cirrhosis and HCC. Despite progress in the clinical management of chronic liver diseases, pharmacological treatment options for patients with liver cirrhosis and/or advanced HCC are still limited. With their potential to regulate whole networks of genes, miRNA might be used as novel therapeutics in these patients but could also serve as biomarkers for improved patient stratification. In this review, we discuss available data on the role of miRNA in the transition from liver cirrhosis to HCC. We highlight opportunities for clinical translation and discuss open issues applicable to future developments.

Keywords: biomarker; hepatocellular carcinoma; miRNA; translational.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use
  • Carcinogenesis / genetics*
  • Carcinoma, Hepatocellular / etiology
  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / therapy
  • Cell Transformation, Neoplastic
  • Clinical Trials as Topic
  • Gene Expression Regulation, Neoplastic
  • Hepatitis, Chronic / complications
  • Hepatitis, Chronic / genetics
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use
  • Immunotherapy
  • Liver Cirrhosis / complications
  • Liver Cirrhosis / genetics*
  • Liver Neoplasms / etiology
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / therapy
  • Mice
  • MicroRNAs / genetics*
  • MicroRNAs / therapeutic use
  • Neoplasm Proteins / antagonists & inhibitors
  • Oligonucleotides / therapeutic use
  • Protein Kinase Inhibitors / therapeutic use
  • RNA, Neoplasm / genetics*
  • Xenograft Model Antitumor Assays

Substances

  • Antineoplastic Agents
  • Immune Checkpoint Inhibitors
  • MicroRNAs
  • Neoplasm Proteins
  • Oligonucleotides
  • Protein Kinase Inhibitors
  • RNA, Neoplasm
  • miravirsen