Target intelligence / Profile preview

Extracellular vesicle (Exosome) (EV)

Target
EV
Molecular classification
Extracellular vesicle, Lipid bilayer, Signal transduction vehicle
01

Overview

Extracellular vesicles (EVs), including exosomes, are nano-sized, membrane-bound particles (30–150 nm) secreted by almost all cell types into the extracellular environment (Kalluri & LeBleu, 2020, Science). They serve as critical mediators of intercellular communication by transporting a diverse cargo of proteins, lipids, and various RNA species, such as microRNA and messenger RNA, to recipient cells (Pegtel & Gould, 2019, Annu Rev Biochem). In the context of disease, exosomes play a dual role; they can facilitate the progression of cancer by remodeling the tumor microenvironment and promoting metastasis, or they can contribute to neurodegenerative processes by spreading misfolded proteins like tau or alpha-synuclein (Théry et al., 2018, J Extracell Vesicles). From a therapeutic perspective, the targets involved in exosome-mediated signaling are often heterogeneous, involving the vesicle's surface ligands and the internal cargo that interacts with intracellular pathways upon uptake. Current pharmacological strategies involve either inhibiting the biogenesis and release of pathogenic exosomes using small molecules like GW4869 or engineering synthetic and cell-derived exosomes to deliver specific therapeutic payloads to target tissues (Kalluri & LeBleu, 2020, Science). Because exosomes can cross biological barriers, including the blood-brain barrier, they represent a sophisticated mechanism for targeted drug delivery, although the complexity of their heterogeneous targets presents significant challenges for standardization and safety (Pegtel & Gould, 2019, Annu Rev Biochem).

Other names
ExosomesMicrovesiclesEctosomesSecretory vesiclesNanovesiclesExtracellular vesicle-mediated signaling
02

Mechanism of action

Facilitation of horizontal transfer of bioactive molecules (proteins, lipids, and nucleic acids) to recipient cells via endocytosis, direct fusion, or receptor-ligand interactions (Kalluri & LeBleu, 2020, Science; Pegtel & Gould, 2019, Annu Rev Biochem).

03

Biological functions

Intercellular communicationSignal transductionProtein transportRNA transportImmune response modulation
04

Disease associations

CancerNeurodegenerative diseaseInflammationCardiovascular diseaseInfection
05

Safety considerations

Heterogeneity of vesicle populationsPotential for off-target effectsRapid clearance by the mononuclear phagocyte systemImmunogenicity of allogeneic vesicles
06

Interacting drugs

GW4869

4 more in the full profile.

07

Biomarkers

CD63CD81CD9TSG101Alix

Beyond the preview

Go deeper on Extracellular vesicle (Exosome) (EV).

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Extracellular vesicle (Exosome) (EV).

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call