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Green tea catechin (−)-epicatechin gallate induces tumour suppressor protein ATF3 via EGR-1 activation

DC Field Value Language
dc.contributor.author윤주헌-
dc.date.accessioned2014-12-21T16:35:41Z-
dc.date.available2014-12-21T16:35:41Z-
dc.date.issued2007-
dc.identifier.issn0959-8049-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/95981-
dc.description.abstractEpicatechin gallate (ECG) is the third major catechin component in green tea, but it shows strong biological activity in some aspects, including apoptosis, cell growth inhibition, and membrane transport system in various cells. We previously reported that ECG induces activating transcription factor 3 (ATF3), which is involved in pro-apoptosis in HCT-116 cells. In this report, we present a molecular mechanism by which ECG induces ATF3 expression at the transcriptional level. We found that Sp3 contributed to the basal expression of the ATF3 gene, whereas EGR-1 played an important role in ECG-induced ATF3 expression in HCT-116 cells, as assessed by EMSA and co-transfection experiments. These results suggested that EGR-1, a tumour suppressor protein, could substantiate ECG’s role of ATF3 expression in human colorectal cancer cells. We also found that pro-oxidant activity of ECG contributed to ECG-induced ATF3 expression.-
dc.description.statementOfResponsibilityopen-
dc.format.extent2404~2412-
dc.relation.isPartOfEUROPEAN JOURNAL OF CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHActivating Transcription Factor 3/metabolism*-
dc.subject.MESHAntioxidants/pharmacology*-
dc.subject.MESHApoptosis/drug effects-
dc.subject.MESHCamellia sinensis*-
dc.subject.MESHCatechin/analogs & derivatives*-
dc.subject.MESHCatechin/pharmacology-
dc.subject.MESHEarly Growth Response Protein 1/metabolism*-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHTea*-
dc.subject.MESHTumor Suppressor Protein p53/metabolism-
dc.titleGreen tea catechin (−)-epicatechin gallate induces tumour suppressor protein ATF3 via EGR-1 activation-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Otorhinolaryngology (이비인후과학)-
dc.contributor.googleauthorKyou-Nam Cho-
dc.contributor.googleauthorMugdha Sukhthankar-
dc.contributor.googleauthorSeung Joon Baek-
dc.contributor.googleauthorJoo-Heon Yoon-
dc.contributor.googleauthorSeong-Ho Lee-
dc.identifier.doi10.1016/j.ejca.2007.07.020-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA02604-
dc.relation.journalcodeJ00809-
dc.identifier.eissn1879-0852-
dc.identifier.pmid17764926-
dc.identifier.urlhttp://www.sciencedirect.com/science/article/pii/S095980490700559X-
dc.contributor.alternativeNameYoon, Joo Heon-
dc.contributor.affiliatedAuthorYoon, Joo Heon-
dc.rights.accessRightsnot free-
dc.citation.volume43-
dc.citation.number16-
dc.citation.startPage2404-
dc.citation.endPage2412-
dc.identifier.bibliographicCitationEUROPEAN JOURNAL OF CANCER, Vol.43(16) : 2404-2412, 2007-
dc.identifier.rimsid35350-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers

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