Communication in tiny packages: Exosomes as means of tumor-stroma communication

Biochim Biophys Acta Rev Cancer. 2020 Apr;1873(2):188340. doi: 10.1016/j.bbcan.2020.188340. Epub 2020 Jan 8.

Abstract

Tumor-derived exosomes are nano-sized vesicles acting as multi-signal devices influencing tumor growth at local and distant sites. Exosomes are derived from the endolysosomal compartment and can shuttle diverse biomolecules like nucleic acids (microRNAs and DNA fragments), lipids, proteins, and even pharmacological compounds from a donor cell to recipient cells. The transfer of cargo to recipient cells enables tumor-derived exosomes to influence diverse cellular functions like proliferation, cell survival, and migration in recipient cells, highlighting tumor-derived exosomes as important players in communication within the tumor microenvironment and at distant sites. In this review, we discuss the mechanisms associated with exosome biogenesis and cargo sorting. In addition, we highlight the communication of tumor-derived exosomes in the tumor microenvironment during different phases of tumor development, focusing on angiogenesis, immune escape mechanisms, drug resistance, and metastasis.

Keywords: Communication; Exosomes; Metastasis; Tumor microenvironment; Tumor-derived exosomes; Tumor-stroma.

Publication types

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

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Carcinogenesis / genetics
  • Carcinogenesis / immunology
  • Carcinogenesis / pathology*
  • Cell Communication*
  • Cell Movement
  • Cell Proliferation
  • Cell Survival
  • DNA, Neoplasm / metabolism
  • Drug Resistance, Neoplasm
  • Exosomes / metabolism*
  • Humans
  • Lipid Metabolism
  • MicroRNAs / metabolism
  • Neoplasm Metastasis
  • Neoplasms / drug therapy
  • Neoplasms / genetics
  • Neoplasms / immunology
  • Neoplasms / pathology*
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / immunology
  • Neovascularization, Pathologic / pathology
  • Tumor Escape
  • Tumor Microenvironment*

Substances

  • Antineoplastic Agents
  • DNA, Neoplasm
  • MicroRNAs