Current Understanding of Exosomal MicroRNAs in Glioma Immune Regulation and Therapeutic Responses

Front Immunol. 2022 Jan 14:12:813747. doi: 10.3389/fimmu.2021.813747. eCollection 2021.

Abstract

Exosomes, the small extracellular vesicles, are released by multiple cell types, including tumor cells, and represent a novel avenue for intercellular communication via transferring diverse biomolecules. Recently, microRNAs (miRNAs) were demonstrated to be enclosed in exosomes and therefore was protected from degradation. Such exosomal miRNAs can be transmitted to recipient cells where they could regulate multiple cancer-associated biological processes. Accumulative evidence suggests that exosomal miRNAs serve essential roles in modifying the glioma immune microenvironment and potentially affecting the malignant behaviors and therapeutic responses. As exosomal miRNAs are detectable in almost all kinds of biofluids and correlated with clinicopathological characteristics of glioma, they might be served as promising biomarkers for gliomas. We reviewed the novel findings regarding the biological functions of exosomal miRNAs during glioma pathogenesis and immune regulation. Furthermore, we elaborated on their potential clinical applications as biomarkers in glioma diagnosis, prognosis and treatment response prediction. Finally, we summarized the accessible databases that can be employed for exosome-associated miRNAs identification and functional exploration of cancers, including glioma.

Keywords: biomarker; exosomes; glioma; microRNAs; therapeutic response.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Biomarkers, Tumor
  • Cell Communication
  • Cell Proliferation
  • Databases, Genetic
  • Disease Management
  • Disease Susceptibility
  • Exosomes / metabolism*
  • Glioma / etiology*
  • Glioma / metabolism*
  • Glioma / pathology
  • Glioma / therapy
  • Humans
  • Immunomodulation*
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Molecular Targeted Therapy
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / metabolism
  • RNA Transport
  • Signal Transduction

Substances

  • Biomarkers, Tumor
  • MicroRNAs