Exosome-mediated communication in the tumor microenvironment contributes to hepatocellular carcinoma development and progression

J Hematol Oncol. 2019 May 29;12(1):53. doi: 10.1186/s13045-019-0739-0.

Abstract

The tumor microenvironment (TME) is an essential intrinsic portion of hepatocellular carcinoma (HCC) for the regulation of its origination, development, invasion, and metastasis. As emerging components of the tumor-host interaction, exosomes are increasingly recognized as professional carriers of information in TME and as pivotal molecular entities involved in tumorigenic microenvironment setup. However, much remains unknown about the role of the exosome communication system within TME in the development and progression of HCC. In this review, we focus on the roles and probable mechanisms of TME in HCC and show the exosome-based immune regulation in TME to promote HCC. Multiple processes are involved in HCC, including tumor survival, growth, angiogenesis, invasion, and metastasis. We also discuss the specific roles of exosomes in HCC processes by molding hospitable TME for HCC, such as providing energy, transmitting protumor signals, and evading inhibitory signals. In addition, exosomes induce angiogenesis by changing the biological characteristics of endothelial cells and directly regulating proangiogenic and propermeability factors. Furthermore, exosomes may lead to HCC metastatic invasion by epithelial-mesenchymal transformation, extracellular matrix degradation, and vascular leakage. Finally, we summarize the therapeutic usage of exosomes in the HCC microenvironment and attempt to provide a theoretical reference for modern antitumor agents designed to target these mechanisms.

Keywords: Exosomes; Hepatocellular carcinoma; Immune regulation; Therapy; Tumor microenvironment.

Publication types

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

MeSH terms

  • Animals
  • Carcinogenesis / immunology
  • Carcinogenesis / pathology
  • Carcinoma, Hepatocellular / immunology
  • Carcinoma, Hepatocellular / pathology*
  • Disease Progression
  • Exosomes / immunology
  • Exosomes / pathology*
  • Humans
  • Liver Neoplasms / immunology
  • Liver Neoplasms / pathology*
  • Neoplasm Invasiveness / immunology
  • Neoplasm Invasiveness / pathology
  • Neovascularization, Pathologic / immunology
  • Neovascularization, Pathologic / pathology
  • Tumor Microenvironment*