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GALNT11 as a new molecular marker in chronic lymphocytic leukemia
Authors:MG Libisch  M Casás  ML Chiribao  P Moreno  A Cayota  E Osinaga  P Oppezzo  C Robello
Institution:1. Molecular Biology Unit, Institut Pasteur de Montevideo, Montevideo, Uruguay;2. Cancer Research, AstraZeneca R&D, Boston, USA;3. Biochemistry Department, School of Medicine, Universidad de la República, Montevideo, Uruguay;4. Recombinant Protein Unit, Institut Pasteur de Montevideo, Montevideo, Uruguay;5. Molecular Oncology Unit, Institut Pasteur de Montevideo, Montevideo, Uruguay;6. Immunology Department, School of Medicine, Universidad de la República, Montevideo, Uruguay;g Tumor Immunology and Glycobiology Laboratory, Institut Pasteur de Montevideo, Montevideo, Uruguay
Abstract:Aberrant mucin O-glycosylation often occurs in different cancers and is characterized by immature expression of simple mucin-type carbohydrates. At present, there are some controversial reports about the Tn antigen (GalNAcα-O-Ser/Thr) expression and there is a great lack of information about the UDP-N-acetyl-α-d-galactosamine:polypeptide N-acetylgalactosaminyltransferase (GalNAc-Ts)] expression in chronic lymphocytic leukemia (CLL). To gain insight in these issues we evaluated the Tn antigen expression in CLL patient samples using two Tn binding proteins with different fine specificity. We also studied the expression from 14 GalNAc-Ts genes in CLL patients by RT-PCR. Our results have provided additional information about the expression level of the Tn antigen, suggesting that a low density of Tn residues is expressed in CLL cells. We also found that GALNT11 was expressed in CLL cells and normal T cell whereas little or no expression was found in normal B cells. Based on these results, GALNT11 expression was assessed by qPCR in a cohort of 50 CLL patients. We found significant over-expression of GALNT11 in 96% of B–CLL cells when compared to normal B cells. Moreover, we confirmed the expression of this enzyme at the protein level. Finally we found that GALNT11 expression was significantly associated with the mutational status of the immunoglobulin heavy chain variable region (IGHV), ?2(1) = 18.26; P < 0.0001], lipoprotein lipase expression ?2(1) = 13.72; P = 0.0002] and disease prognosis ?2(1) = 15.49; P < 0.0001]. Our evidence suggests that CLL patient samples harbor aberrant O-glycosylation highlighted by Tn antigen expression and that the over-expression of GALNT11 constitutes a new molecular marker for CLL.
Keywords:aa  amino acid(s)  bp  base pair  BSA  bovine serum albumin  CD19  cluster of differentiation 19  CD3  cluster of differentiation 3  cDNA  DNA complementary to RNA  CLL  chronic lymphocytic leukemia  FBS  fetal bovine serum  GalNAc-Ts  UDP-N-acetyl-α-d-galactosamine:polypeptide N-acetylgalactosaminyltransferase  GALNT11  Gene that encode GalNAc-T11  GAPDH  Glyceraldehyde 3-phosphate dehydrogenase  Ig  immunoglobulin(s)  IGHV  immunoglobulin heavy chain variable region  IIF  indirect immunofluorescence  LPL  lipoprotein lipase  mAB  monoclonal Antibody  MMLV  Moloney Murine Leukemia Virus  Mut  mutated  PAGE  PA-gel electrophoresis  PB  peripheral blood  PBMCs  peripheral blood mononuclear cells  PBS  phosphate-buffered saline  PCA  peptide competition assay  qPCR  quantitative real time PCR  REST  Relative Expression Software Tool  SDS  sodium dodecyl sulfate  UM  unmutated  VVB4  isolectin B4 from Vicia villosa  ZAP-70  zeta-associated protein 70
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