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dc.creatorHadzidimitriou, A.en
dc.creatorStamatopoulos, K.en
dc.creatorBelessi, C.en
dc.creatorLalayianni, C.en
dc.creatorStavroyianni, N.en
dc.creatorSmilevska, T.en
dc.creatorHatzi, K.en
dc.creatorLaoutaris, N.en
dc.creatorAnagnostopoulos, A.en
dc.creatorKollia, P.en
dc.creatorFassas, A.en
dc.date.accessioned2015-11-23T10:29:25Z
dc.date.available2015-11-23T10:29:25Z
dc.date.issued2006
dc.identifier.issn3906078
dc.identifier.urihttp://hdl.handle.net/11615/28299
dc.description.abstractBackground and Objectives. The available data on the immunoglobulin gene (IG) repertoire in multiple myeloma (MM) derive mainly from heavy chains; considerably less is known about light chains. We assessed in parallel IGH and IGK/IGL rearrangements in 101 MM patients so as to gain insight into: (i) IG repertoires; (ii) antigen impact; (iii) the role of receptor editing. Design and Methods. Bone marrow aspirates were collected from all cases. IGHV-(D)-J and IGLV-J rearrangements were amplified by reverse transcriptase polymerase chain reaction (PCR). In all cases, IGKV-J rearrangements were analyzed in parallel on cDNA/genomic DNA. IGKV-KDE and IGKJ-C-INTRON-KDE were also amplified by DNA-PCR. RT-PCR products were directly sequenced. Results. IGHV3 genes predominated; the IGHV4-34 gene was used in only one case. Five IGKV and five IGLV genes accounted fcr the majority of in-frame, transcribed IGKV-J or IGLV-J rearrangements. Taking IGKV-J, IGKV-KDE and IGKJ-C-INTRON-KDE rearrangements together, biallelic IGK locus rearrangements were detected in 22/43 κ-MM cases. In λ-MMM, 36/42 cases had at least one rearranged IGK allele; 8/19 IGKV-J rearrangements in λ-MM were in-frame. All in-frame, transcribed IGH/IGK/IGL sequences were mutated; parallel heavy/light chain analysis demonstrated a comparable impact of somatic hypermutation. Interpretation and Conclusions. Biases in IG repertoire did not seem disease-related but followed a similar pattern to that of the normal repertoire. The under-representation of the IGHV4-34 gene provides an explanation for the paucity of autoimmune phenomena in MM. Somatic mutation patterns indicate the complementary role of MM IGH/IGK/IGL sequences in antigen recognition. Finally, the frequent inactivation of productive IGKV-J joints by secondary rearrangements in MM suggests active receptor editing. ©2006 Ferrata Storti Foundation.en
dc.sourceHaematologicaen
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-33745757786&partnerID=40&md5=93b72998a0e31214da39afecb5c39a15
dc.subjectκ deleting elementen
dc.subjectImmunoglobulin repertoireen
dc.subjectMultiple myelomaen
dc.subjectantigenen
dc.subjectcomplementary DNAen
dc.subjectgenomic DNAen
dc.subjectreceptoren
dc.subjectalleleen
dc.subjectarticleen
dc.subjectbone marrow biopsyen
dc.subjectcontrolled studyen
dc.subjectgene amplificationen
dc.subjectgene expressionen
dc.subjectgene locusen
dc.subjectgene mutationen
dc.subjectgene rearrangementen
dc.subjectgene sequenceen
dc.subjectgenetic transcriptionen
dc.subjectheavy chainen
dc.subjecthumanen
dc.subjectimmunoglobulin geneen
dc.subjectintronen
dc.subjectlight chainen
dc.subjectmajor clinical studyen
dc.subjectreverse transcription polymerase chain reactionen
dc.subjectsomatic mutationen
dc.subjectBone Marrow Cellsen
dc.subjectDatabases, Nucleic Aciden
dc.subjectGenes, Immunoglobulinen
dc.subjectHumansen
dc.subjectImmunoglobulin Heavy Chainsen
dc.subjectImmunoglobulin Light Chainsen
dc.subjectMutationen
dc.subjectPolymerase Chain Reactionen
dc.subjectReverse Transcriptase Polymerase Chain Reactionen
dc.titleImmunoglobulin genes in multiple myeloma: Expressed and non-expressed repertoires, heavy and light chain pairings and somatic mutation patterns in a series of 101 casesen
dc.typejournalArticleen


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