Enhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer

Cited 8 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorDong Hyun Kim-
dc.contributor.authorHye-Min Kim-
dc.contributor.authorP T T Huong-
dc.contributor.authorHo Jin Han-
dc.contributor.authorJoonsung Hwang-
dc.contributor.authorHyunjoo Cha-
dc.contributor.authorKyung Ho Lee-
dc.contributor.authorIn Ja Ryoo-
dc.contributor.authorK E Kim-
dc.contributor.authorY H Huh-
dc.contributor.authorJong Seog Ahn-
dc.contributor.authorY T Kwon-
dc.contributor.authorNak Kyun Soung-
dc.contributor.authorBo Yeon Kim-
dc.date.accessioned2019-07-10T01:23:36Z-
dc.date.available2019-07-10T01:23:36Z-
dc.date.issued2019-
dc.identifier.issn1225-8687-
dc.identifier.uri10.5483/BMBRep.2019.52.5.055ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/18820-
dc.description.abstractMethylation 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.publisherKorea Soc-Assoc-Inst-
dc.titleEnhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer-
dc.title.alternativeEnhanced anticancer effects of a methylation inhibitor by inhibiting a novel DNMT1 target, CEP 131, in cervical cancer-
dc.typeArticle-
dc.citation.titleBMB Reports-
dc.citation.number5-
dc.citation.endPage347-
dc.citation.startPage342-
dc.citation.volume52-
dc.contributor.affiliatedAuthorDong Hyun Kim-
dc.contributor.affiliatedAuthorHye-Min Kim-
dc.contributor.affiliatedAuthorHo Jin Han-
dc.contributor.affiliatedAuthorJoonsung Hwang-
dc.contributor.affiliatedAuthorHyunjoo Cha-
dc.contributor.affiliatedAuthorKyung Ho Lee-
dc.contributor.affiliatedAuthorIn Ja Ryoo-
dc.contributor.affiliatedAuthorJong Seog Ahn-
dc.contributor.affiliatedAuthorNak Kyun Soung-
dc.contributor.affiliatedAuthorBo Yeon Kim-
dc.contributor.alternativeName김동현-
dc.contributor.alternativeName김혜민-
dc.contributor.alternativeNameHuong-
dc.contributor.alternativeName한호진-
dc.contributor.alternativeName황준성-
dc.contributor.alternativeName차현주-
dc.contributor.alternativeName이경호-
dc.contributor.alternativeName류인자-
dc.contributor.alternativeName김균언-
dc.contributor.alternativeName허양훈-
dc.contributor.alternativeName안종석-
dc.contributor.alternativeName권용태-
dc.contributor.alternativeName성낙균-
dc.contributor.alternativeName김보연-
dc.identifier.bibliographicCitationBMB Reports, vol. 52, no. 5, pp. 342-347-
dc.identifier.doi10.5483/BMBRep.2019.52.5.055-
dc.subject.keywordAnti-cancer-
dc.subject.keywordCentrosome-
dc.subject.keywordCEP131-
dc.subject.keywordDNMT1-
dc.subject.localAnti-cancer-
dc.subject.localAnticancer-
dc.subject.localanti-cancer-
dc.subject.localanticancer-
dc.subject.localAnti-Cancer-
dc.subject.localCentrosome-
dc.subject.localCEP131-
dc.subject.localDnmt1-
dc.subject.localDNMT1-
dc.subject.localDnmt1s-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
Ochang Branch Institute > Nucleic Acid Therapeutics Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.