iRGD 1392278-76-0 98%
iRGDpeptide-mediatedtumorpenetrationoccursinthreesteps:bindingtoαv-integrinsontumorvasculatureortumorcells,exposurebyproteolysisofaC-terminalmotifthatbindstoneuropilin-1(NRP-1)andcellinternalization.iRGDpeptideinsertedintheICOVIR15KfiberCterminusenhancesbindingandinternalizationonlyinMCF7cells,whichexpressNRP-1andintegrins.iRGDinsertiondoesnotimpairvirusinfectionandreplication.iRGDpeptidealonehasnoobviouseffeChemicalbookctongastriccancercells,andwhencombinedwith5-FU,iRGDpeptide(0.3μmol/mL)enhancesthechemotherapyefficacyof5-FUongastriccancercellsthroughNRP1.体内研究iRGDinsertedintheoncolyticadenovirusICOVIR15K(ICOVIR15K-iRGD)enhancesearlyadenovirusdisseminationthroughthetumormassandelevatestheantitumoreffectinmice.iRGD(4mmol/kg,i.v.)incombinationwith5-FUsignificantlysuppressesthetumorgrowthinnudemicebearinghumangastriccancercells.
iRGDpeptide-mediatedtumorpenetrationoccursinthreesteps:bindingtoαv-integrinsontumorvasculatureortumorcells,exposurebyproteolysisofaC-terminalmotifthatbindstoneuropilin-1(NRP-1)andcellinternalization.iRGDpeptideinsertedintheICOVIR15KfiberCterminusenhancesbindingandinternalizationonlyinMCF7cells,whichexpressNRP-1andintegrins.iRGDinsertiondoesnotimpairvirusinfectionandreplication.iRGDpeptidealonehasnoobviouseffeChemicalbookctongastriccancercells,andwhencombinedwith5-FU,iRGDpeptide(0.3μmol/mL)enhancesthechemotherapyefficacyof5-FUongastriccancercellsthroughNRP1.体内研究iRGDinsertedintheoncolyticadenovirusICOVIR15K(ICOVIR15K-iRGD)enhancesearlyadenovirusdisseminationthroughthetumormassandelevatestheantitumoreffectinmice.iRGD(4mmol/kg,i.v.)incombinationwith5-FUsignificantlysuppressesthetumorgrowthinnudemicebearinghumangastriccancercells.
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