Recent advances in conventional and unconventional vesicular secretion pathways in the tumor microenvironment

J Biomed Sci. 2022 Aug 5;29(1):56. doi: 10.1186/s12929-022-00837-8.

Abstract

All cells in the changing tumor microenvironment (TME) need a class of checkpoints to regulate the balance among exocytosis, endocytosis, recycling and degradation. The vesicular trafficking and secretion pathways regulated by the small Rab GTPases and their effectors convey cell growth and migration signals and function as meditators of intercellular communication and molecular transfer. Recent advances suggest that Rab proteins govern conventional and unconventional vesicular secretion pathways by trafficking widely diverse cargoes and substrates in remodeling TME. The mechanisms underlying the regulation of conventional and unconventional vesicular secretion pathways, their action modes and impacts on the cancer and stromal cells have been the focus of much attention for the past two decades. In this review, we discuss the current understanding of vesicular secretion pathways in TME. We begin with an overview of the structure, regulation, substrate recognition and subcellular localization of vesicular secretion pathways. We then systematically discuss how the three fundamental vesicular secretion processes respond to extracellular cues in TME. These processes are the conventional protein secretion via the endoplasmic reticulum-Golgi apparatus route and two types of unconventional protein secretion via extracellular vesicles and secretory autophagy. The latest advances and future directions in vesicular secretion-involved interplays between tumor cells, stromal cell and host immunity are also described.

Keywords: Exocytosis; Extracellular vesicle; Rab GTPase; Secretory autophagy; Tumor microenvironment; Vesicle trafficking.

Publication types

  • Review

MeSH terms

  • Endoplasmic Reticulum / metabolism
  • Golgi Apparatus / metabolism
  • Protein Transport
  • Secretory Pathway*
  • Tumor Microenvironment*
  • rab GTP-Binding Proteins / metabolism

Substances

  • rab GTP-Binding Proteins