Non-coding RNAs shuttled via exosomes reshape the hypoxic tumor microenvironment

J Hematol Oncol. 2020 Jun 5;13(1):67. doi: 10.1186/s13045-020-00893-3.

Abstract

Exosomes are small extracellular vesicles secreted by almost all the cells. Molecular cargos of exosomes can partially reflect the characteristics of originating cells. Exosome-mediated cell-to-cell interactions in the microenvironment are critical in cancer progression. Hypoxia, a key pro-cancerous feature of the tumor microenvironment, alters the releasing and contents of exosomes. A growing body of evidence shows that hypoxia induces more aggressive phenotypes in cancer. Of note, non-coding RNAs shuttled in hypoxic tumor-derived exosomes have been demonstrated as fundamental molecules in regulating cancer biology and remodeling tumor microenvironment. Furthermore, these hypoxic tumor-derived exosomal non-coding RNAs can be detected in the body fluids, serving as promising diagnostic and prognostic biomarkers. The current review discusses changes in cancer behaviors regulated by exosomes-secreted non-coding RNAs under hypoxic conditions.

Keywords: Exosomes; Hypoxia; LncRNA; MiRNA; Non-coding RNA; Tumor microenvironment.

Publication types

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

MeSH terms

  • Biomarkers, Tumor
  • Cell Division / genetics
  • Cell Hypoxia / genetics*
  • Drug Resistance, Neoplasm / genetics
  • Exocytosis
  • Exosomes / metabolism*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Liquid Biopsy
  • Neoplasm Invasiveness / genetics
  • Neoplasm Metastasis
  • Neoplasm Proteins / metabolism
  • Neoplasms / blood supply
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Neoplasms / pathology*
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / metabolism
  • Prognosis
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism*
  • RNA, Untranslated / genetics
  • RNA, Untranslated / metabolism*
  • Stromal Cells / metabolism
  • Stromal Cells / pathology
  • Tumor Escape / genetics
  • Tumor Microenvironment / genetics*

Substances

  • Biomarkers, Tumor
  • Neoplasm Proteins
  • RNA, Neoplasm
  • RNA, Untranslated