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Distinct gene expression profiles in subsets of chronic lymphocytic leukemia expressing stereotyped IGHV4-34 B-cell receptors

  • Millaray Marincevic
  • Mahmoud Mansouri
  • Meena Kanduri
  • Anders Isaksson
  • Hanna Goransson
  • Karin Ekstrom Smedby
  • Jesper Jurlander
  • Gunnar Juliusson
  • Fred Davi
  • Kostas Stamatopoulos
  • Richard Rosenquist
Publiceringsår: 2010
Språk: Engelska
Sidor: 2072-2079
Publikation/Tidskrift/Serie: Haematologica
Volym: 95
Nummer: 12
Dokumenttyp: Artikel i tidskrift
Förlag: Ferrata Storti Foundation


Background Numerous subsets of patients with chronic lymphocytic leukemia display similar immunoglobulin gene usage with almost identical complementarity determining region 3 sequences. Among IGHV4-34 cases, two such subsets with "stereotyped" B-cell receptors were recently identified, i.e. subset #4 (IGHV4-34/IGKV2-30) and subset #16 (IGHV4-34/IGKV3-20). Subset #4 patients appear to share biological and clinical features, e.g. young age at diagnosis and indolent disease, whereas little is known about subset #16 at a clinical level. Design and Methods We investigated the global gene expression pattern in sorted chronic lymphocytic leukemia cells from 25 subset/non-subset IGHV4-34 patients using Affymetrix gene expression arrays. Results Although generally few differences were found when comparing subset to non-subset 4/16 IGHV4-34 cases, distinct gene expression profiles were revealed for subset #4 versus subset #16. The differentially expressed genes, predominantly with lower expression in subset #4 patients, are involved in important cell regulatory pathways including cell-cycle control, proliferation and immune response, which may partly explain the low-proliferative disease observed in subset #4 patients. Conclusions Our novel data demonstrate distinct gene expression profiles among patients with stereotyped IGHV4-34 B-cell receptors, providing further evidence for biological differences in the pathogenesis of these subsets and underscoring the functional relevance of subset assignment based on B-cell receptor sequence features.


  • Hematology
  • expression
  • gene
  • chronic lymphocytic leukemia
  • IGHV(4)-34
  • stereotyped BCR


  • ISSN: 1592-8721

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