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Repression of human telomerase reverse transcriptase using artificial zinc finger transcription factors

DC Field Value Language
dc.contributor.author박광균-
dc.date.accessioned2015-04-23T16:58:45Z-
dc.date.available2015-04-23T16:58:45Z-
dc.date.issued2010-
dc.identifier.issn1541-7786-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/101594-
dc.description.abstractTelomerase activation is a key step in the development of human cancers. Expression of the catalytic subunit, human telomerase reverse transcriptase (hTERT), represents the limiting factor for telomerase activity. In this study, we have used artificial zinc finger protein (ZFP) transcription factors (TF) to repress the expression of hTERT in human cancer cell lines at the transcriptional level. We have constructed four-fingered ZFPs derived from the human genome which binds 12-bp recognition sequences within the promoter of the hTERT gene and fused them with a KRAB repressor domain to create a potent transcriptional repressor. Luciferase activity was decreased by >80% in all of the transcriptional repressors with luciferase reporter assay. When they were transfected into the telomerase-positive HEK293 cell line, a decrease of mRNA level and telomerase activity together with shortening of telomere length was observed. Actual growth of HEK293 cells was also inhibited by transfection of artificial ZFP-TFs. The repression was maintained for 100 days of culture. The repression of telomerase expression by artificial ZFP-TFs targeting the promoter region of the hTERT presents a new promising strategy for inhibiting the growth of human cancer cells-
dc.description.statementOfResponsibilityopen-
dc.format.extent246~253-
dc.relation.isPartOfMOLECULAR CANCER RESEARCH-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAntineoplastic Agents/chemical synthesis-
dc.subject.MESHAntineoplastic Agents/metabolism-
dc.subject.MESHBinding Sites/genetics-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCell Transformation, Neoplastic/genetics*-
dc.subject.MESHGene Targeting/methods-
dc.subject.MESHGrowth Inhibitors/chemical synthesis-
dc.subject.MESHGrowth Inhibitors/genetics-
dc.subject.MESHGrowth Inhibitors/metabolism-
dc.subject.MESHHumans-
dc.subject.MESHPromoter Regions, Genetic/drug effects-
dc.subject.MESHPromoter Regions, Genetic/genetics-
dc.subject.MESHRNA, Messenger/metabolism-
dc.subject.MESHRegulatory Elements, Transcriptional/genetics-
dc.subject.MESHRepressor Proteins/chemical synthesis-
dc.subject.MESHRepressor Proteins/genetics*-
dc.subject.MESHRepressor Proteins/metabolism-
dc.subject.MESHTelomerase/genetics*-
dc.subject.MESHTelomerase/metabolism-
dc.subject.MESHTranscription Factors/chemical synthesis-
dc.subject.MESHTranscription Factors/genetics*-
dc.subject.MESHTranscription Factors/metabolism-
dc.subject.MESHTransfection-
dc.subject.MESHZinc Fingers/genetics*-
dc.titleRepression of human telomerase reverse transcriptase using artificial zinc finger transcription factors-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry (치과대학)-
dc.contributor.departmentDept. of Oral Biology (구강생물학)-
dc.contributor.googleauthorJoon Hyung Sohn-
dc.contributor.googleauthorByung-Il Yeh-
dc.contributor.googleauthorJong-Whan Choi-
dc.contributor.googleauthorJoonho Yoon-
dc.contributor.googleauthorJun Namkung-
dc.contributor.googleauthorKwang-Kyun Park-
dc.contributor.googleauthorHyun-Won Kim-
dc.identifier.doi10.1158/1541-7786.MCR-09-0141-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01429-
dc.relation.journalcodeJ02253-
dc.identifier.eissn1557-3125-
dc.identifier.pmid20145034-
dc.contributor.alternativeNamePark, Kwang Kyun-
dc.contributor.affiliatedAuthorPark, Kwang Kyun-
dc.citation.volume8-
dc.citation.number2-
dc.citation.startPage246-
dc.citation.endPage253-
dc.identifier.bibliographicCitationMOLECULAR CANCER RESEARCH, Vol.8(2) : 246-253, 2010-
dc.identifier.rimsid40107-
dc.type.rimsART-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Biology (구강생물학교실) > 1. Journal Papers

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