Overexpression of TOSO in CLL is triggered by B-cell receptor signaling and associated with progressive disease

Blood. 2008 Nov 15;112(10):4213-9. doi: 10.1182/blood-2008-05-157255. Epub 2008 Aug 15.

Abstract

Resistance toward apoptotic stimuli mediated by overexpression of antiapoptotic factors or extracellular survival signals is considered to be responsible for accumulation of malignant B cells in chronic lymphocytic leukemia (CLL). TOSO was identified as overexpressed candidate gene in CLL, applying unit-transformation assays of publicly available microarray datasets. Based on CLL samples from 106 patients, TOSO was identified to exhibit elevated relative expression (RE) of 6.8 compared with healthy donor B cells using quantitative real-time polymerase chain reaction (PCR; P = .004). High levels of TOSO expression in CLL correlated with high leukocyte count, advanced Binet stage, previous need for chemotherapy, and unmutated IgV(H) status. CD38(+) CLL subsets harboring proliferative activity showed enhanced TOSO expression. We evaluated functional mechanisms of aberrant TOSO expression and identified TOSO expression significantly induced by B-cell receptor (BCR) stimulation compared with control cells (RE; 8.25 vs 4.86; P = .01). In contrast, CD40L signaling significantly reduced TOSO expression (RE, 2.60; P = .01). In summary, we show that the antiapoptotic factor TOSO is associated with progressive disease and enhanced in the proliferative CD38(+) CLL subset. Both association with unmutated IgV(H) and the specific induction of TOSO via the BCR suggest autoreactive BCR signaling as a key mediator of apoptosis resistance in CLL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-ribosyl Cyclase 1 / metabolism
  • Apoptosis
  • Apoptosis Regulatory Proteins / biosynthesis*
  • B-Lymphocytes / metabolism*
  • B-Lymphocytes / pathology
  • Disease Progression
  • Female
  • Gene Expression Regulation, Leukemic*
  • Humans
  • Immunoglobulin Heavy Chains / metabolism
  • Immunoglobulin Variable Region / metabolism
  • Leukemia, Lymphocytic, Chronic, B-Cell / metabolism*
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology
  • Male
  • Membrane Glycoproteins / metabolism
  • Membrane Proteins / biosynthesis*
  • Neoplasm Proteins / biosynthesis*
  • Receptors, Antigen, B-Cell / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction*

Substances

  • Apoptosis Regulatory Proteins
  • FCMR protein, human
  • Immunoglobulin Heavy Chains
  • Immunoglobulin Variable Region
  • Membrane Glycoproteins
  • Membrane Proteins
  • Neoplasm Proteins
  • Receptors, Antigen, B-Cell
  • CD38 protein, human
  • ADP-ribosyl Cyclase 1