Publication:
Cordycepin induces apoptosis of C6 glioma cells through the adenosine 2A receptor-p53-caspase-7-PARP pathway

cris.lastimport.scopus2025-05-14T22:43:27Z
cris.virtual.departmentSurgery-NTUHen_US
cris.virtual.departmentSurgeryen_US
cris.virtual.orcid0000-0002-8572-4977en_US
cris.virtualsource.departmentad16a595-bf64-4a89-a664-8f3bbf8e68bc
cris.virtualsource.departmentad16a595-bf64-4a89-a664-8f3bbf8e68bc
cris.virtualsource.orcidad16a595-bf64-4a89-a664-8f3bbf8e68bc
dc.contributor.authorChen Y.en_US
dc.contributor.authorSHIH-HUNG YANGen_US
dc.contributor.authorHueng D.-Y.en_US
dc.contributor.authorSyu J.-P.en_US
dc.contributor.authorLiao C.-C.en_US
dc.contributor.authorWu Y.-C.en_US
dc.creatorChen Y.;Shih-Hung Yang;Hueng D.-Y.;Syu J.-P.;Liao C.-C.;Wu Y.-C.
dc.date.accessioned2020-03-17T03:00:57Z
dc.date.available2020-03-17T03:00:57Z
dc.date.issued2014
dc.description.abstractCordycepin, 3′-deoxyadenosine from Cordyceps sinensis, has been shown to exert anti-tumor effects in several cancer cell lines. This study investigated the effect of cordycepin on a rat glioma cell line. Cordycepin caused apoptosis in C6 glioma cells in a time- and concentration-dependent manner, but did not affect the survival of primary cultured rat astrocytes. Cordycepin increased the total protein levels of p53 and phosphorylated p53 in the C6 cells. Levels of cleaved caspase-7 and poly (ADP-ribose) polymerase (PARP), but not cleaved caspase-3, were also increased after cordycepin treatment. Specific inhibitors for p53 and caspases abrogated cordycepin-induced caspase-7 and PARP cleavage, and prevented cordycepin-induced apoptosis. Moreover, siRNA knockdown of p53 blocked cordycepin-induced cleavage of caspase-7 and PARP. Both adenosine 2A receptor (A2AR) antagonist and small interference RNA (siRNA) knockdown of A2AR blocked cordycepin-induced apoptosis, p53 activation, and caspase-7 and PARP cleavage. These may provide a new strategy of cordycepin for glioma therapy in the future. ? 2014 Elsevier Ireland Ltd. All rights reserved.
dc.identifier.doi10.1016/j.cbi.2014.03.010
dc.identifier.issn0009-2797
dc.identifier.pmid24704558
dc.identifier.scopus2-s2.0-84898983728
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84898983728&doi=10.1016%2fj.cbi.2014.03.010&partnerID=40&md5=90d2e88fe63add27ece15482d46cb015
dc.identifier.urihttps://scholars.lib.ntu.edu.tw/handle/123456789/476333
dc.publisherElsevier Ireland Ltd
dc.relation.ispartofChemico-Biological Interactions
dc.relation.journalissue1
dc.relation.journalvolume216
dc.relation.pages17-25
dc.subject.classification[SDGs]SDG3
dc.subject.otheradenosine A2 receptor; caspase 3; caspase 7; cordycepin; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase; protein p53; small interfering RNA; animal cell; apoptosis; article; astrocyte; cell survival; cell viability; concentration response; controlled study; glioma cell; nonhuman; protein cleavage; protein phosphorylation; rat; signal transduction; Adenosine 2A receptor; Apoptosis; Cordycepin; Glioma; p53; Animals; Antineoplastic Agents; Apoptosis; Caspase 7; Cell Line, Tumor; Cell Survival; Deoxyadenosines; Gene Expression Regulation, Neoplastic; Glioma; Poly(ADP-ribose) Polymerases; Rats; Receptors, Adenosine A2; RNA Interference; RNA, Small Interfering; Tumor Suppressor Protein p53
dc.titleCordycepin induces apoptosis of C6 glioma cells through the adenosine 2A receptor-p53-caspase-7-PARP pathwayen_US
dc.typejournal articleen
dspace.entity.typePublication

Files