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Helicobacter pylori gamma-glutamyltranspeptidase induces cell cycle arrest at the G1-S phase transition

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dc.contributor.authorKim, Kyung-Mi-
dc.contributor.authorLee, Seung-Gyu-
dc.contributor.authorKim, Jung-Min-
dc.contributor.authorKim, Do-Su-
dc.contributor.authorSong, Jea-Young-
dc.contributor.authorKang, Hyung-Lyun-
dc.contributor.authorLee, Woo-Kon-
dc.contributor.authorCho, Myung-Je-
dc.contributor.authorRhee, Kwang-Ho-
dc.contributor.authorYoun, Hee-Shang-
dc.contributor.authorBaik, Seung-Chul-
dc.date.accessioned2022-12-27T04:10:21Z-
dc.date.available2022-12-27T04:10:21Z-
dc.date.issued2010-06-
dc.identifier.issn1225-8873-
dc.identifier.issn1976-3794-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/25080-
dc.description.abstractIn our previous study, we showed that Helicobacter pylori gamma-glutamyltranspeptidase (GGT) is associated with H. pylori-induced apoptosis through a mitochondrial pathway. To better understand the role of GGT in apoptosis, we examined the effect of GGT on cell cycle regulation in AGS cells. To determine the effect of recombinant GGT (rGGT) on cell cycle distribution and apoptosis, rGGT-treated and untreated AGS cells were analyzed in parallel by flow cytometry using propidium iodide (PI). We found that rGGT inhibited the growth of AGS cells in a time-dependent manner, and that the pre-exposure of cells to a caspase-3 inhibitor (z-DEVD-fmk) effectively blocked GGT-induced apoptosis. Cell cycle analysis showed G1 phase arrest and apoptosis in AGS cells following rGGT treatment. The rGGT-mediated G1 phase arrest was found to be associated with down-regulation of cyclin E, cyclin A, Cdk 4, and Cdk 6, and the up-regulation of the cyclindependent kinase (Cdk) inhibitors p27 and p21. Our results suggest that H. pylori GGT induces cell cycle arrest at the G1-S phase transition.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherMICROBIOLOGICAL SOCIETY KOREA-
dc.titleHelicobacter pylori gamma-glutamyltranspeptidase induces cell cycle arrest at the G1-S phase transition-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1007/s12275-010-9293-8-
dc.identifier.scopusid2-s2.0-77953966515-
dc.identifier.wosid000279087800015-
dc.identifier.bibliographicCitationJOURNAL OF MICROBIOLOGY, v.48, no.3, pp 372 - 377-
dc.citation.titleJOURNAL OF MICROBIOLOGY-
dc.citation.volume48-
dc.citation.number3-
dc.citation.startPage372-
dc.citation.endPage377-
dc.type.docTypeArticle-
dc.identifier.kciidART001460940-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusCYTOLETHAL DISTENDING TOXIN-
dc.subject.keywordPlusDEPENDENT KINASES-
dc.subject.keywordPlusCDK INHIBITORS-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusCARCINOGENESIS-
dc.subject.keywordPlusPROGRESSION-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordAuthorH. pylori-
dc.subject.keywordAuthorgamma-glutamyltranspeptidase-
dc.subject.keywordAuthorcell cycle-
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