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dc.contributor.author최한곤-
dc.date.accessioned2018-12-06T05:05:06Z-
dc.date.available2018-12-06T05:05:06Z-
dc.date.issued2008-11-
dc.identifier.citationMOLECULAR AND CELLULAR BIOCHEMISTRY, v. 318, No. 1-2, Page. 23-31en_US
dc.identifier.issn0300-8177-
dc.identifier.urihttps://link.springer.com/article/10.1007/s11010-008-9853-y-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/80756-
dc.description.abstractPharmacological depletion of L-gamma-glutamyl-L-cysteinyl-glycine (GSH) has been implicated in the sensitization of cancer cells to alkylating agents and apoptosis. However, some types of cells do not induce apoptotic response following chemical depletion of GSH. In the present study, we report that murine embryonic fibroblasts (MEFs) can survive in the presence of GSH inhibitor L-buthionine(S,R)-sulfoximine (BSO), even though most intracellular GSH was depleted. As a cellular adaptive mechanism, BSO treatment effectively activated the NF-E2-related factor 2 (Nrf2) pathway, which led to up-regulation of antioxidant enzymes in these cells through the extracellular signal-regulated kinase cascade. While nrf2-deficient MEFs lost the inducibility of antioxidant genes, which resulted in higher levels of reactive oxygen species accumulation, caspase-3 activation, and cell death than wild-type cells. Finally, nrf2-deficient cells can be more sensitized to doxorubicin-induced cell death by BSO pre-incubation, while wild-type cells were not. In addition, BSO-mediated cell death was facilitated by administering Nrf2 siRNA to chemoresistant human ovarian cancer cells. These results indicate that Nrf2 is the primary factor inducing the cell survival system under GSH depletion and that the effect of BSO as a chemosensitizer might be enhanced by inhibition of Nrf2.en_US
dc.description.sponsorshipThis work was supported by the Korea Science and Engineering Foundation (KOSEF) grant funded by the Korea government (MOST, R01-2007-000-10890-0)en_US
dc.language.isoen_USen_US
dc.publisherSPRINGERen_US
dc.subjectGSHen_US
dc.subjectBSOen_US
dc.subjectOxidative stressen_US
dc.subjectNrf2en_US
dc.subjectChemosensitizeren_US
dc.titleAdaptive response to GSH depletion and resistance to L-buthionine-(S,R)-sulfoximine: involvement of Nrf2 activationen_US
dc.typeArticleen_US
dc.relation.no1-2-
dc.relation.volume318-
dc.identifier.doi10.1007/s11010-008-9853-y-
dc.relation.page23-31-
dc.relation.journalMOLECULAR AND CELLULAR BIOCHEMISTRY-
dc.contributor.googleauthorLee, Hyang-Rim-
dc.contributor.googleauthorCho, Jeong-Min-
dc.contributor.googleauthorShin, Dong-ha-
dc.contributor.googleauthorYong, Chul Soon-
dc.contributor.googleauthorChoi, Han-Gon-
dc.contributor.googleauthorWakabayashi, Nobunao-
dc.contributor.googleauthorKwak, Mi-Kyoung-
dc.relation.code2008206797-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF PHARMACY[E]-
dc.sector.departmentDEPARTMENT OF PHARMACY-
dc.identifier.pidhangon-
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COLLEGE OF PHARMACY[E](약학대학) > PHARMACY(약학과) > Articles
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