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dc.contributor.authorPetridou, E.en
dc.contributor.authorKlimentopoulou, A. E.en
dc.contributor.authorMoustaki, M.en
dc.contributor.authorKostrikis, Leontios G.en
dc.contributor.authorHatzakis, Angelos E.en
dc.contributor.authorTrichopoulos, D.en
dc.creatorPetridou, E.en
dc.creatorKlimentopoulou, A. E.en
dc.creatorMoustaki, M.en
dc.creatorKostrikis, Leontios G.en
dc.creatorHatzakis, Angelos E.en
dc.creatorTrichopoulos, D.en
dc.date.accessioned2019-11-04T12:52:28Z
dc.date.available2019-11-04T12:52:28Z
dc.date.issued2002
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53301
dc.description.abstractThe concentration of T-cell receptor rearrangement excision DNA circles (TRECs) in peripheral blood mononuclear cells (PBMCs) is currently known to be a marker of recent thymic emigrants. We evaluated the hypothesis that TREC values would be lower in childhood T-cell hematopoietic malignancies than in childhood B-cell acute lymphoblastic leukemia (ALL) or healthy controls because the former category may reflect compromised thymic function. From the Greek national childhood leukemia/lymphoma database we obtained all 30 available T-cell leukemia/non-Hodgkin's lymphoma cases, 30 age- and sex-matched childhood B-cell origin cases of ALL and 60 healthy hospital controls. We compared TREC levels in PBMCs using a real-time PCR assay. There was highly significant reduction of TREC values in children with T-cell malignancies (median 3,100 TRECs/106 PBMCs), whereas children with B-cell origin ALL had slightly but nonsignificantly lower TREC values compared to healthy children (medians 19,300 and 22,500 TRECs/106 PBMCs, respectively). During a median follow-up period of about 19 months, only 4 children died. All of them had a T-cell hematopoietic malignancy and relatively low TREC values. The number of TRECs was higher among healthy girls than among healthy boys, and a similar pattern was evident in T-cell malignancies. It appears that there is a pattern of concordance of high TREC values with better disease prognosis in hematologic childhood malignancies. This applies to specific disease entities with better prognosis (B-cell origin ALL having higher TREC values than T-cell leukemia/lymphoma) and to gender, another important predictor of prognosis conditional on disease entity (girls having higher TREC values than boys)en
dc.description.abstracthowever, it may also be true for the survival of individual patients. These preliminary findings can be used as hypothesis-generating indications that should be confirmed in larger data sets. © 2002 Wiley-Liss, Inc.en
dc.sourceInternational Journal of Canceren
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0036722798&doi=10.1002%2fijc.10568&partnerID=40&md5=900a944637a0986170e7c8535f8630d2
dc.subjectarticleen
dc.subjecthumanen
dc.subjectHumansen
dc.subjectcontrolled studyen
dc.subjectfemaleen
dc.subjectmajor clinical studyen
dc.subjectfollow upen
dc.subjectpriority journalen
dc.subjectprognosisen
dc.subjectSurvival Rateen
dc.subjectnonhodgkin lymphomaen
dc.subjectmaleen
dc.subjectLymphomaen
dc.subjectChilden
dc.subjectT-Lymphocytesen
dc.subjectDNAen
dc.subjectpolymerase chain reactionen
dc.subjectLeukemiaen
dc.subjectschool childen
dc.subjectCell Movementen
dc.subjectDNA, Neoplasmen
dc.subjectthymusen
dc.subjectThymus Glanden
dc.subjectReceptors, Antigen, T-Cellen
dc.subjectT lymphocyte receptoren
dc.subjectGene Rearrangement, T-Lymphocyteen
dc.subjectAge of Onseten
dc.subjectAcute lymphoblastic leukemiaen
dc.subjectB cell leukemiaen
dc.subjectB-Lymphocytesen
dc.subjectchildhood leukemiaen
dc.subjectLeukemia, Lymphocytic, Acuteen
dc.subjectSex Characteristicsen
dc.subjectT cell leukemiaen
dc.subjectT-cell receptor rearrangement excision circleen
dc.subjectThymic emigranten
dc.titleRecent thymic emigrants and prognosis in T- and B-cell childhood hematopoietic malignanciesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/ijc.10568
dc.description.volume101
dc.description.startingpage74
dc.description.endingpage77
dc.author.facultyΣχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Βιολογικών Επιστημών / Department of Biological Sciences
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :21</p>en
dc.source.abbreviationInt.J.Canceren
dc.contributor.orcidKostrikis, Leontios G. [0000-0002-5340-7109]
dc.gnosis.orcid0000-0002-5340-7109


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