Phosphatidylserine receptor-targeting therapies for the treatment of cancer.
Miso ParkKeon Wook KangPublished in: Archives of pharmacal research (2019)
Asymmetric distribution of phospholipids across the plasma membrane is a unique characteristic of eukaryotic cells. Phosphatidylcholine and sphingomyelin are exposed in the outer leaflet, and phosphatidylserine (PS) is predominantly located in the inner leaflet. Redistribution of PS to the cell surface can be observed in several physiological conditions, such as apoptosis and platelet activation, or in pathological conditions, such as the release of microvesicles/exosomes from tumor tissues. PS binding to the phosphatidylserine receptor (PSR) on immune cells initiates immunosuppressive pathways that can lead to immune evasion by cancer cells. Conversely, PSR activation of cancer cells plays an important role in their survival, proliferation and metastasis. Herein, we briefly summarize both recent advances in our understanding of the pathological roles of PS and its receptor in cancer biology, as well as relevant pharmacological approaches.
Keyphrases
- papillary thyroid
- cell surface
- cell cycle arrest
- aortic valve
- induced apoptosis
- squamous cell
- oxidative stress
- stem cells
- endoplasmic reticulum stress
- gene expression
- mesenchymal stem cells
- signaling pathway
- squamous cell carcinoma
- binding protein
- heart failure
- atrial fibrillation
- pi k akt
- childhood cancer
- left ventricular
- replacement therapy