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TUCAN: An anti-apoptotic CARD family protein over-expressed in cancer

DC Field Value Language
dc.contributor.author김호근-
dc.date.accessioned2016-02-19T11:11:05Z-
dc.date.available2016-02-19T11:11:05Z-
dc.date.issued2001-
dc.identifier.issn0021-9258-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/142585-
dc.description.abstractCaspase-associated recruitment domains (CARDs) are protein interaction domains that participate in activation or suppression of CARD-carrying members of the caspase family of apoptosis-inducing proteases. A novel CARD-containing protein was identified that is overexpressed in some types of cancer and that binds and suppresses activation of procaspase-9, which we term TUCAN (tumor-up-regulated CARD-containing antagonist of caspase nine). The CARD domain of TUCAN selectively binds itself and procaspase-9. TUCAN interferes with binding of Apaf1 to procaspase-9 and suppresses caspase activation induced by the Apaf1 activator, cytochrome c. Overexpression of TUCAN in cells by stable or transient transfection inhibits apoptosis and caspase activation induced by Apaf1/caspase-9-dependent stimuli, including Bax, VP16, and staurosporine, but not by Apaf1/caspase-9-independent stimuli, Fas and granzyme B. High levels of endogenous TUCAN protein were detected in several tumor cell lines and in colon cancer specimens, correlating with shorter patient survival. Thus, TUCAN represents a new member of the CARD family that selectively suppresses apoptosis induced via the mitochondrial pathway for caspase activation.-
dc.description.statementOfResponsibilityopen-
dc.format.extent32220~32229-
dc.relation.isPartOfJOURNAL OF BIOLOGICAL CHEMISTRY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleTUCAN: An anti-apoptotic CARD family protein over-expressed in cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학)-
dc.contributor.googleauthorNuzhat Pathan-
dc.contributor.googleauthorHiroyuki Marusawa-
dc.contributor.googleauthorMaryla Krajewska-
dc.contributor.googleauthorShu-ichi Matsuzawa-
dc.contributor.googleauthorHoguen Kim-
dc.contributor.googleauthorKazuya Okada-
dc.contributor.googleauthorSeiji Torii-
dc.contributor.googleauthorShinichi Kitada-
dc.contributor.googleauthorStanislaw Krajewski-
dc.contributor.googleauthorKate Welsh-
dc.contributor.googleauthorFrederick Pio-
dc.contributor.googleauthorAdam Godzik-
dc.contributor.googleauthorJohn C. Reed-
dc.identifier.doi10.1074/jbc.M100433200-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01183-
dc.relation.journalcodeJ01258-
dc.identifier.eissn1083-351X-
dc.contributor.alternativeNameKim, Ho Keun-
dc.contributor.affiliatedAuthorKim, Ho Keun-
dc.rights.accessRightsfree-
dc.citation.volume276-
dc.citation.number34-
dc.citation.startPage32220-
dc.citation.endPage32229-
dc.identifier.bibliographicCitationJOURNAL OF BIOLOGICAL CHEMISTRY, Vol.276(34) : 32220-32229, 2001-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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