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Indoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: A retrospective cohort study

DC Field Value Language
dc.contributor.author김세훈-
dc.date.accessioned2015-01-06T16:55:35Z-
dc.date.available2015-01-06T16:55:35Z-
dc.date.issued2014-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/99037-
dc.description.abstractBACKGROUND: Regulation of tumor microenvironment is closely involved in the prognosis of Hodgkin lymphoma (HL). Indoleamine 2,3-dioxygenase (IDO) is an enzyme acting as immune modulator through suppression of T-cell immunity. This study aims to investigate role of IDO in the microenvironment of HL. METHODS: A total of 121 cases of HL were enrolled to do immunohistochemistry for IDO, CD163, CD68, CD4, CD8, and FoxP3. Positivity was evaluated from area fractions or numbers of positive cells using automated image analyzer. Correlations between IDO expression and various cellular infiltrates and clinicopathologic parameters were examined and survival analyses were performed. RESULTS: IDO was expressed in histiocytes, dendritic cells and some endothelial cells with variable degrees, but not in tumor cells. IDO positive cells were more frequently found in mixed cellularity type than other histologic types, and in cases with EBV+, high Ann Arbor stages, B symptoms, and high IPS (all p < 0.05). High IDO expression was associated with inferior survival (p < 0.001) and reflects an independent prognostic factor in nodular sclerosis HL. CONCLUSIONS: This is the first study suggesting that IDO is the principle immunomodulator and is involved to adverse clinical outcomes of HL.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1~9-
dc.relation.isPartOfBMC CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdolescent-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHBiomarkers, Tumor/analysis-
dc.subject.MESHBiopsy-
dc.subject.MESHCell Lineage-
dc.subject.MESHChild-
dc.subject.MESHDisease-Free Survival-
dc.subject.MESHFemale-
dc.subject.MESHHodgkin Disease/enzymology*-
dc.subject.MESHHodgkin Disease/mortality-
dc.subject.MESHHodgkin Disease/pathology-
dc.subject.MESHHumans-
dc.subject.MESHImmunohistochemistry-
dc.subject.MESHIndoleamine-Pyrrole 2,3,-Dioxygenase/analysis*-
dc.subject.MESHKaplan-Meier Estimate-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHProportional Hazards Models-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHStromal Cells/enzymology*-
dc.subject.MESHStromal Cells/pathology-
dc.subject.MESHTime Factors-
dc.subject.MESHTumor Microenvironment-
dc.subject.MESHYoung Adult-
dc.titleIndoleamine 2,3-dioxygenase (IDO) is frequently expressed in stromal cells of Hodgkin lymphoma and is associated with adverse clinical features: A retrospective cohort study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학)-
dc.contributor.googleauthorJi-Young Choe-
dc.contributor.googleauthorJi Yun Yun-
dc.contributor.googleauthorYoon Kyoung Jeon-
dc.contributor.googleauthorSe Hoon Kim-
dc.contributor.googleauthorGyeongsin Park-
dc.contributor.googleauthorJoo Ryoung Huh-
dc.contributor.googleauthorSohee Oh-
dc.contributor.googleauthorJi Eun Kim-
dc.identifier.doi10.1186/1471-2407-14-335-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00610-
dc.relation.journalcodeJ00351-
dc.identifier.eissn1471-2407-
dc.identifier.pmid24886161-
dc.subject.keywordHodgkin disease-
dc.subject.keywordIndoleamine-pyrrole 2,3-dioxygenase-
dc.subject.keywordMacrophages-
dc.subject.keywordStromal cells-
dc.subject.keywordTumor microenvironment-
dc.subject.keywordEpstein-barr virus infections-
dc.subject.keywordPathology-
dc.contributor.alternativeNameKim, Se Hoon-
dc.contributor.affiliatedAuthorKim, Se Hoon-
dc.citation.volume14-
dc.citation.number335-
dc.citation.startPage1-
dc.citation.endPage9-
dc.identifier.bibliographicCitationBMC CANCER, Vol.14(335) : 1-9, 2014-
dc.identifier.rimsid50225-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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