ATM mutations in major stereotyped subsets of chronic lymphocytic leukemia: enrichment in subset #2 is associated with markedly short telomeres.

نویسندگان

  • Veronika Navrkalova
  • Emma Young
  • Panagiotis Baliakas
  • Lenka Radova
  • Lesley-Ann Sutton
  • Karla Plevova
  • Larry Mansouri
  • Viktor Ljungström
  • Stavroula Ntoufa
  • Zadie Davis
  • Gunnar Juliusson
  • Karin E Smedby
  • Chrysoula Belessi
  • Panagiotis Panagiotidis
  • Tasoula Touloumenidou
  • Frederic Davi
  • Anton W Langerak
  • Paolo Ghia
  • Jonathan C Strefford
  • David Oscier
  • Jiri Mayer
  • Kostas Stamatopoulos
  • Sarka Pospisilova
  • Richard Rosenquist
  • Martin Trbusek
چکیده

by Veronika Navrkalova, Emma Young, Panagiotis Baliakas, Lenka Radova, Lesley-Ann Sutton, Karla Plevova, Larry Mansouri, Viktor Ljungström, Stavroula Ntoufa, Zadie Davies, Gunnar Juliusson, Karin E. Smedby, Chrysoula Belessi, Panagiotis Panagiotidis, Tasoula Touloumenidou, Frederic Davi, Anton W. Langerak, Paolo Ghia, Jonathan C. Strefford, David Oscier, Jiri Mayer, Kostas Stamatopoulos, Sarka Pospisilova, Richard Rosenquist, and Martin Trbusek

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Recurrent cytogenetic findings in subsets of patients with chronic lymphocytic leukemia expressing IgG-switched stereotyped immunoglobulins.

We report a remarkable association of recurrent (stereotyped) cytogenetic aberrations with two subsets of chronic lymphocytic leukemia (CLL) cases expressing IgG-switched, stereotyped B-cell receptors (BCRs). Comparison with cases with heterogeneous BCRs showed that these recurrent cytogenetic aberrations were subset-biased. These findings further support a role for antigen in CLL development.

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

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 biol...

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عنوان ژورنال:
  • Haematologica

دوره 101 9  شماره 

صفحات  -

تاریخ انتشار 2016