Research advances of tissue-derived extracellular vesicles in cancers

J Cancer Res Clin Oncol. 2024 Apr 10;150(4):184. doi: 10.1007/s00432-023-05596-z.

Abstract

Background: Extracellular vesicles (EVs) can mediate cell-to-cell communication and affect various physiological and pathological processes in both parent and recipient cells. Currently, extensive research has focused on the EVs derived from cell cultures and various body fluids. However, insufficient attention has been paid to the EVs derived from tissues. Tissue EVs can reflect the microenvironment of the specific tissue and the cross-talk of communication among different cells, which can provide more accurate and comprehensive information for understanding the development and progression of diseases.

Methods: We review the state-of-the-art technologies involved in the isolation and purification of tissue EVs. Then, the latest research progress of tissue EVs in the mechanism of tumor occurrence and development is presented. And finally, the application of tissue EVs in the clinical diagnosis and treatment of cancer is anticipated.

Results: We evaluate the strengths and weaknesses of various tissue processing and EVs isolation methods, and subsequently analyze the significance of protein characterization in determining the purity of tissue EVs. Furthermore, we focus on outlining the importance of EVs derived from tumor and adipose tissues in tumorigenesis and development, as well as their potential applications in early tumor diagnosis, prognosis, and treatment.

Conclusion: When isolating and characterizing tissue EVs, the most appropriate protocol needs to be specified based on the characteristics of different tissues. Tissue EVs are valuable in the diagnosis, prognosis, and treatment of tumors, and the potential risks associated with tissue EVs need to be considered as therapeutic agents.

Keywords: Cancer diagnosis and treatment; Density gradient centrifugation; Enzymatic digestion; Tissue culture; Tissue-derived extracellular vesicles.

Publication types

  • Review

MeSH terms

  • Body Fluids*
  • Carcinogenesis
  • Cell Communication
  • Extracellular Vesicles*
  • Humans
  • Neoplasms*
  • Tumor Microenvironment