DC Field | Value | Language |
---|---|---|
dc.contributor.author | Dong Hyun Kim | - |
dc.contributor.author | Hye-Min Kim | - |
dc.contributor.author | P T T Huong | - |
dc.contributor.author | Ho Jin Han | - |
dc.contributor.author | Joonsung Hwang | - |
dc.contributor.author | Hyunjoo Cha | - |
dc.contributor.author | Kyung Ho Lee | - |
dc.contributor.author | In Ja Ryoo | - |
dc.contributor.author | K E Kim | - |
dc.contributor.author | Y H Huh | - |
dc.contributor.author | Jong Seog Ahn | - |
dc.contributor.author | Y T Kwon | - |
dc.contributor.author | Nak Kyun Soung | - |
dc.contributor.author | Bo Yeon Kim | - |
dc.date.accessioned | 2019-07-10T01:23:36Z | - |
dc.date.available | 2019-07-10T01:23:36Z | - |
dc.date.issued | 2019 | - |
dc.identifier.issn | 1225-8687 | - |
dc.identifier.uri | 10.5483/BMBRep.2019.52.5.055 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/18820 | - |
dc.description.abstract | Methylation is a primary epigenetic mechanism regulating gene expression. 5-aza-2'-deoxycytidine is an FDA-approved drug prescribed for treatment of cancer by inhibiting DNA-Methyl-Transferase 1 (DNMT1). Results of this study suggest that prolonged treatment with 5-aza-2'-deoxycytidine could induce centrosome abnormalities in cancer cells and that CEP131, a centrosome protein, is regulated by DNMT1. Interestingly, cancer cell growth was attenuated in vitro and in vivo by inhibiting the expression of Cep131. Finally, Cep131-deficient cells were more sensitive to treatment with DNMT1 inhibitors. These findings suggest that Cep131 is a potential novel anti-cancer target. Agents that can inhibit this protein may be useful alone or in combination with DNMT1 inhibitors to treat cancer. | - |
dc.publisher | Korea Soc-Assoc-Inst | - |
dc.title | Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer | - |
dc.title.alternative | Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer | - |
dc.type | Article | - |
dc.citation.title | BMB Reports | - |
dc.citation.number | 5 | - |
dc.citation.endPage | 347 | - |
dc.citation.startPage | 342 | - |
dc.citation.volume | 52 | - |
dc.contributor.affiliatedAuthor | Dong Hyun Kim | - |
dc.contributor.affiliatedAuthor | Hye-Min Kim | - |
dc.contributor.affiliatedAuthor | Ho Jin Han | - |
dc.contributor.affiliatedAuthor | Joonsung Hwang | - |
dc.contributor.affiliatedAuthor | Hyunjoo Cha | - |
dc.contributor.affiliatedAuthor | Kyung Ho Lee | - |
dc.contributor.affiliatedAuthor | In Ja Ryoo | - |
dc.contributor.affiliatedAuthor | Jong Seog Ahn | - |
dc.contributor.affiliatedAuthor | Nak Kyun Soung | - |
dc.contributor.affiliatedAuthor | Bo Yeon Kim | - |
dc.contributor.alternativeName | 김동현 | - |
dc.contributor.alternativeName | 김혜민 | - |
dc.contributor.alternativeName | Huong | - |
dc.contributor.alternativeName | 한호진 | - |
dc.contributor.alternativeName | 황준성 | - |
dc.contributor.alternativeName | 차현주 | - |
dc.contributor.alternativeName | 이경호 | - |
dc.contributor.alternativeName | 류인자 | - |
dc.contributor.alternativeName | 김균언 | - |
dc.contributor.alternativeName | 허양훈 | - |
dc.contributor.alternativeName | 안종석 | - |
dc.contributor.alternativeName | 권용태 | - |
dc.contributor.alternativeName | 성낙균 | - |
dc.contributor.alternativeName | 김보연 | - |
dc.identifier.bibliographicCitation | BMB Reports, vol. 52, no. 5, pp. 342-347 | - |
dc.identifier.doi | 10.5483/BMBRep.2019.52.5.055 | - |
dc.subject.keyword | Anti-cancer | - |
dc.subject.keyword | Centrosome | - |
dc.subject.keyword | CEP131 | - |
dc.subject.keyword | DNMT1 | - |
dc.subject.local | Anti-cancer | - |
dc.subject.local | Anticancer | - |
dc.subject.local | anti-cancer | - |
dc.subject.local | anticancer | - |
dc.subject.local | Anti-Cancer | - |
dc.subject.local | Centrosome | - |
dc.subject.local | CEP131 | - |
dc.subject.local | Dnmt1 | - |
dc.subject.local | DNMT1 | - |
dc.subject.local | Dnmt1s | - |
dc.description.journalClass | Y | - |
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