341 607

Cited 0 times in

HOXB5 Directly Regulates the Expression of IL-6 in MCF7 Breast Cancer Cells

DC Field Value Language
dc.contributor.author김명희-
dc.contributor.author김지민-
dc.contributor.author이지연-
dc.date.accessioned2018-07-20T08:10:45Z-
dc.date.available2018-07-20T08:10:45Z-
dc.date.issued2017-
dc.identifier.issn1738-3226-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/160932-
dc.description.abstractPurpose: Among the survivors of a ST elevation myocardial infarction (STEMI), higher platelet volume indices (mean platelet volume, MPV; platelet distribution width, PDW) are associated with impaired reperfusion and ventricular dysfunction. This study examined the relationship between the platelet volume indices and 30-day mortality with STEMI patients who underwent primary percutaneous coronary intervention (PCI). Methods: This retrospective cohort study included patients presenting to the emergency department with STEMI between January 2011 and May 2016. The platelet volume indices were measured serially, using an automatic hematology analyzer, from admission to 24 hours after admission. The prognostic value of MPV, PDW for the 30-day mortality was determined by Cox proportional hazards model analysis. Results: A total of 608 STEMI patients, who underwent reperfusion, were enrolled in this study. According to the multivariable Cox proportional hazard model, higher MPV (hazard ratio [HR], 1.414; 95% confidence interval [CI], 1.024-1.953; p=0.035) and PDW (HR, 1.043; 95% CI, 1.006-1.083; p=0.024) values at time-24 (24 hours after admission) were significant risk factors for the 30-day mortality. A MPV value >8.6 fL (HR, 5.953; 95% CI, 2.973-11.918; p< 0.001) and PDW value >56.1% (HR, 5.117; 95% CI, 2.640-9.918; p<0.001) at time-24 were associated with an increased risk of 30-day mortality. Conclusion: The platelet volume indices without an additional burden of cost or time, can be measured rapidly and simply. Higher MPV and PDW levels predict independently the 30-day mortality in patients with STEMI after PCI.-
dc.description.statementOfResponsibilityopen-
dc.languageKorean, English-
dc.publisherKorean Society For Biomedical Laboratory Sciences-
dc.relation.isPartOfJournal of Experimental & Biomedcal Science (대한의생명과학회지)-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleHOXB5 Directly Regulates the Expression of IL-6 in MCF7 Breast Cancer Cells-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Anatomy-
dc.contributor.googleauthorKim Jie Min-
dc.contributor.googleauthorLee Ji-Yeon-
dc.contributor.googleauthorKim Myoung Hee-
dc.identifier.doi10.15616/BSL.2017.23.3.272-
dc.contributor.localIdA00432-
dc.contributor.localIdA05320-
dc.contributor.localIdA03194-
dc.relation.journalcodeJ01408-
dc.subject.keywordBreast cancer-
dc.subject.keywordHOXB5-
dc.subject.keywordIL-6-
dc.subject.keywordTranscription-
dc.contributor.alternativeNameKim, Myoung Hee-
dc.contributor.alternativeNameKim, Jie Min-
dc.contributor.alternativeNameLee, Ji Yeon-
dc.contributor.affiliatedAuthorKim, Myoung Hee-
dc.contributor.affiliatedAuthorKim, Jie Min-
dc.contributor.affiliatedAuthorLee, Ji Yeon-
dc.citation.volume23-
dc.citation.number3-
dc.citation.startPage272-
dc.citation.endPage276-
dc.identifier.bibliographicCitationJournal of Experimental & Biomedcal Science (대한의생명과학회지), Vol.23(3) : 272-276, 2017-
dc.identifier.rimsid60808-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Anatomy (해부학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.