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A novel activation-induced suicidal degradation mechanism for Akt by selenium

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dc.contributor.authorLee, Ji-Hyun-
dc.contributor.authorShin, Sun Hye-
dc.contributor.authorKang, Seongman-
dc.contributor.authorLee, Yun-Sil-
dc.contributor.authorBae, Sangwoo-
dc.date.accessioned2021-09-09T13:01:31Z-
dc.date.available2021-09-09T13:01:31Z-
dc.date.created2021-06-15-
dc.date.issued2008-01-
dc.identifier.issn1107-3756-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/124514-
dc.description.abstractSelenium has been associated with an anti-cancer effect via the modulation of Akt. In order to investigate whether selenium modulates Akt by hitherto unidentified molecular mechanisms, we examined the effect of selenium on the stability and activity of Akt. Selenium induced destabilization of Akt which is coupled to its own enzyme activation. Mutation of T308 and S473 of Akt to alanine as well as the inhibition or depletion of upstream kinases for Akt activation blocked Akt degradation. These features of Akt degradation are reminiscent of the 'activation-induced suicidal degradation' mechanism. PTEN was also required for Akt destabilization as Akt activation alone was unable to elicit Akt degradation in the absence of PTEN. Conversely, PTEN introduction in PTEN-null prostate cancer cells restored the ability to degrade Akt upon selenium treatment. Collectively, selenium seems to achieve ultimate negative regulation of Akt signaling by destabilizing the protein, and this regulation mechanism might provide a paradigm for the anti-cancer activity of selenium.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherPROFESSOR D A SPANDIDOS-
dc.subjectPROTEIN-KINASE B/AKT-
dc.subjectPROSTATE-CANCER-
dc.subjectCELLS-
dc.subjectPATHWAY-
dc.subjectPHOSPHORYLATION-
dc.subjectAPOPTOSIS-
dc.subjectAKT/PKB-
dc.subjectPTEN-
dc.titleA novel activation-induced suicidal degradation mechanism for Akt by selenium-
dc.typeArticle-
dc.contributor.affiliatedAuthorKang, Seongman-
dc.identifier.scopusid2-s2.0-38949111710-
dc.identifier.wosid000252021200012-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, v.21, no.1, pp.91 - 97-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF MOLECULAR MEDICINE-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR MEDICINE-
dc.citation.volume21-
dc.citation.number1-
dc.citation.startPage91-
dc.citation.endPage97-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.subject.keywordPlusPROTEIN-KINASE B/AKT-
dc.subject.keywordPlusPROSTATE-CANCER-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusAKT/PKB-
dc.subject.keywordPlusPTEN-
dc.subject.keywordAuthorAkt-
dc.subject.keywordAuthorselenium-
dc.subject.keywordAuthoractivation-induced degradation-
dc.subject.keywordAuthorPTEN-
dc.subject.keywordAuthoranti-cancer-
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