The multifaceted role of extracellular vesicles (EVs) in colorectal cancer: metastasis, immune suppression, therapy resistance, and autophagy crosstalk.
Soheil RahmatiAysan MoeinafsharNima RezaeiPublished in: Journal of translational medicine (2024)
Extracellular vesicles (EVs) are lipid bilayer structures released by all cells and widely distributed in all biological fluids. EVs are implicated in diverse physiopathological processes by orchestrating cell-cell communication. Colorectal cancer (CRC) is one of the most common cancers worldwide, with metastasis being the leading cause of mortality in CRC patients. EVs contribute significantly to the advancement and spread of CRC by transferring their cargo, which includes lipids, proteins, RNAs, and DNAs, to neighboring or distant cells. Besides, they can serve as non-invasive diagnostic and prognostic biomarkers for early detection of CRC or be harnessed as effective carriers for delivering therapeutic agents. Autophagy is an essential cellular process that serves to remove damaged proteins and organelles by lysosomal degradation to maintain cellular homeostasis. Autophagy and EV release are coordinately activated in tumor cells and share common factors and regulatory mechanisms. Although the significance of autophagy and EVs in cancer is well established, the exact mechanism of their interplay in tumor development is obscure. This review focuses on examining the specific functions of EVs in various aspects of CRC, including progression, metastasis, immune regulation, and therapy resistance. Further, we overview emerging discoveries relevant to autophagy and EVs crosstalk in CRC.
Keyphrases
- endoplasmic reticulum stress
- induced apoptosis
- cell death
- signaling pathway
- cell cycle arrest
- oxidative stress
- end stage renal disease
- cell therapy
- single cell
- chronic kidney disease
- newly diagnosed
- high resolution
- stem cells
- lymph node
- cardiovascular events
- coronary artery disease
- pi k akt
- squamous cell carcinoma
- peritoneal dialysis
- cardiovascular disease
- type diabetes
- mass spectrometry
- squamous cell
- molecular dynamics
- replacement therapy
- density functional theory
- free survival