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Uridine triphosphate

CAS No.: 63-39-8

Uridine triphosphate (Uridine 5'-triphosphate) increases proliferation of human cancerous pancreatic duct epithelial cel
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Description Uridine triphosphate (Uridine 5'-triphosphate) increases proliferation of human cancerous pancreatic duct epithelial cells by activating P2Y2 receptor.
In vitro Incubation of PANC-1 cells with UTP or MRS2768, a selective P2Y2 receptor agonist, resulted in a dose- and time-dependent increase of proliferation.?The messenger RNA transcript and protein of P2Y2 receptor were expressed in PANC-1 cells.?P2 receptor antagonist suramin and small interfering RNA against P2Y2 receptor significantly decreased the proliferative effect of UTP and MRS2768.?Activation of P2Y2 receptor by UTP transduced to phospholipase C, inositol 1,4,5-triphosphate (IP3), and protein kinase C. Uridine triphosphate-induced proliferation was mediated by protein kinase D, Src-family tyrosine kinase, Ca/calmodulin-dependent protein kinase II, phosphatidylinositol 3-kinase (PI3K), Akt, and phospholipase D. Uridine triphosphate increased phosphorylation of Akt through protein kinase C, Src-family tyrosine kinase, Ca/calmodulin-dependent protein kinase II, and PI3K[1].
Cell experiments Proliferation was measured by immunoassay for bromodeoxyuridine incorporation into the pancreatic cell line PANC-1. Effect of UTP was assayed using selective P2 agonist and antagonist, small interfering RNA, intracellular signal inhibitors, and Western blot[1].
Synonyms 尿苷5'-三磷酸酯, UTP, Uridine 5'-triphosphate, 三磷酸尿苷
molecular weight 484.14
Molecular formula C9H15N2O15P3
CAS 63-39-8
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility H2O: 150 mg/mL (309.83 mM)
References 1. Choi J H , Ji Y G , Lee D H . Uridine Triphosphate Increases Proliferation of Human Cancerous Pancreatic Duct Epithelial Cells by Activating P2Y2 Receptor[J]. Pancreas, 2013, 42(4):680-686. 2. Gündüz Dursun, Christian T , Daniel S , et al. Uridine Triphosphate Thio Analogues Inhibit Platelet P2Y12 Receptor and Aggregation[J]. International Journal of Molecular Sciences, 2017, 18(2):269-.