Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 임형신 | - |
dc.date.accessioned | 2019-06-18T07:24:12Z | - |
dc.date.available | 2019-06-18T07:24:12Z | - |
dc.date.issued | 2007-07 | - |
dc.identifier.citation | APOPTOSIS, v. 12, No. 7, Page. 1229-1241 | en_US |
dc.identifier.issn | 1360-8185 | - |
dc.identifier.issn | 1573-675X | - |
dc.identifier.uri | https://link.springer.com/article/10.1007/s10495-006-0047-3 | - |
dc.identifier.uri | https://repository.hanyang.ac.kr/handle/20.500.11754/106762 | - |
dc.description.abstract | Previous studies have suggested that upregulation of Cyclin A-dependent protein kinase 2 (Cdk2) activity is an essential event in apoptotic progression and the mitochondrial permeability transition in human cancer cells. Here, we show that upregulated Cyclin A/Cdk2 activity precedes the proteolytic cleavage of PARP and is correlated with the mitochondrial translocation of Bax and the loss of mitochondrial transmembrane potential (Delta psi m) during etoposide-induced apoptosis in human cervical adenocarcinoma (HeLa) cells. Etoposide-induced apoptotic cell death is efficiently prevented in cells that overexpress a dominant negative mutant of Cdk2 (Cdk2-dn) or p21(WAF1/CIP1), a specific Cdk inhibitor. Conversely, apoptotic cell death is promoted in Cyclin A-expressing cells. Disruption of the mitochondrial transmembrane potential in etoposide-induced cells is prevented in cells that overexpress Cdk2-dn or p21(WAF1/CIP1), while this transition is prominently promoted in Cyclin A-expressing cells. We screened for mitochondrial Cdk2 targets in the etoposide-induced cells and found that the mitochondrial level of Bax is elevated by more than three fold in etoposide-treated cells and this elevation is effectively prevented in cells expressing Cdk2-dn under the same conditions. Thus, we suggest that Cdk2 activity is involved in the mitochondrial translocation of Bax, which plays an important role in the mitochondrial membrane permeability transition during apoptotic progression. | en_US |
dc.description.sponsorship | This work was supported by the National Research Laboratory Fund (M10104000129-02J000005910) of the Ministry of Science and Technology, Republic of Korea and by the NSFC (grant # 30640064). We thank Dr. Kwang-Yeol Lee (Chonnam National University, Republic Korea) for providing human full-length p21WAF1/CIP1 cDNA and Cdk2-dn cDNA. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | SPRINGER | en_US |
dc.subject | apoptosis | en_US |
dc.subject | Bax | en_US |
dc.subject | Cdk2 activity | en_US |
dc.subject | mitochondrial membrane potential | en_US |
dc.subject | mitochondrial translocation | en_US |
dc.title | Cyclin-dependent protein kinase 2 activity is required for mitochondrial translocation of Bax and disruption of mitochondrial transmembrane potential during etoposide-induced apoptosis | en_US |
dc.type | Article | en_US |
dc.relation.volume | 12 | - |
dc.identifier.doi | 10.1007/s10495-006-0047-3 | - |
dc.relation.page | 1229-1241 | - |
dc.relation.journal | APOPTOSIS | - |
dc.contributor.googleauthor | Choi, Joon-Seok | - |
dc.contributor.googleauthor | Shin, Soona | - |
dc.contributor.googleauthor | Jin, Ying Hua | - |
dc.contributor.googleauthor | Yim, Hyungshin | - |
dc.contributor.googleauthor | Koo, Kyo-Tan | - |
dc.contributor.googleauthor | Chun, Kwang-Hoon | - |
dc.contributor.googleauthor | Oh, You-Take | - |
dc.contributor.googleauthor | Lee, Won Hee | - |
dc.contributor.googleauthor | Lee, Seung-Ki | - |
dc.relation.code | 2007200817 | - |
dc.sector.campus | E | - |
dc.sector.daehak | COLLEGE OF PHARMACY[E] | - |
dc.sector.department | DEPARTMENT OF PHARMACY | - |
dc.identifier.pid | hsyim | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.