Interplay among extracellular vesicles, cancer stemness and immune regulation in driving hepatocellular carcinoma progression

Cancer Lett. 2024 Aug 10:597:217084. doi: 10.1016/j.canlet.2024.217084. Epub 2024 Jun 25.

Abstract

The intricate interplay among extracellular vesicles, cancer stemness properties, and the immune system significantly impacts hepatocellular carcinoma (HCC) progression, treatment response, and patient prognosis. Extracellular vesicles (EVs), which are membrane-bound structures, play a pivotal role in conveying proteins, lipids, and nucleic acids between cells, thereby serving as essential mediators of intercellular communication. Since a lot of current research focuses on small extracellular vesicles (sEVs), with diameters ranging from 30 nm to 200 nm, this review emphasizes the role of sEVs in the context of interactions between HCC stemness-bearing cells and the immune cells. sEVs offer promising opportunities for the clinical application of innovative diagnostic and prognostic biomarkers in HCC. By specifically targeting sEVs, novel therapeutics aimed at cancer stemness can be developed. Ongoing investigations into the roles of sEVs in cancer stemness and immune regulation in HCC will broaden our understanding and ultimately pave the way for groundbreaking therapeutic interventions.

Keywords: Cancer stemness; Extracellular vesicles; Hepatocellular carcinoma; Immune regulation; Interplay.

Publication types

  • Review

MeSH terms

  • Animals
  • Biomarkers, Tumor / immunology
  • Biomarkers, Tumor / metabolism
  • Carcinoma, Hepatocellular* / immunology
  • Carcinoma, Hepatocellular* / metabolism
  • Carcinoma, Hepatocellular* / pathology
  • Cell Communication / immunology
  • Disease Progression*
  • Extracellular Vesicles* / immunology
  • Extracellular Vesicles* / metabolism
  • Humans
  • Liver Neoplasms* / immunology
  • Liver Neoplasms* / metabolism
  • Liver Neoplasms* / pathology
  • Neoplastic Stem Cells* / immunology
  • Neoplastic Stem Cells* / metabolism
  • Neoplastic Stem Cells* / pathology
  • Tumor Microenvironment / immunology

Substances

  • Biomarkers, Tumor