TY - JOUR
T1 - E2A is a transcriptional regulator of CD38 expression in chronic lymphocytic leukemia
AU - Saborit-Villarroya, I.
AU - Vaisitti, T.
AU - Rossi, D.
AU - D'Arena, G.
AU - Gaidano, G.
AU - Malavasi, F.
AU - Deaglio, S.
N1 - Funding Information:
We thank Dr E Ferrero (University of Turin, Italy) and Dr D Colomer (Hospital Clinic, Barcelona, Espana) for expert advice and assistance in setting up the experiments. The expertize of K Gizzi and F Cottino is also gratefully acknowledged. We thank Aczon srl (Bologna, Italy) for labeling monoclonal antibodies produced by the Lab of Immunogenetics. This work was supported by the Associazione Italiana Ricerca Cancro (AIRC, IG8590 and Special Program Molecular and Clinical Oncology, 5 per Mille project), the Compagnia SanPaolo, Ministero della SaluteFBando Giovani Ricercatori 2008, Ministero della Uni-versità e RicercaFBando Futuro in Ricerca 2009, Progetti Ricerca Interesse Nazionale (PRIN) and the Regione Piemonte. The Fondazione Internazionale Ricerche Medicina Sperimentale (FIRMS) provided financial and administrative assistance.
PY - 2011/3
Y1 - 2011/3
N2 - CD38, a nucleotide-metabolizing ectoenzyme and a receptor, is a negative prognostic marker for chronic lymphocytic leukemia (CLL) patients. CD38 has a genetic polymorphism, with a C G variation in a putative E-box located in a regulatory region. E2A, the predominant E-box factor in B lymphocytes, was found to be highly expressed by CD38 CLL patients. The highest CD38 levels scored by E2A /G carrier patients suggested that E2A is (i) directly associated with CD38 expression, and that (ii) the binding of the transcription factor is influenced by the CD38 genotype. Chromatin immunoprecipitation indicated that E2A directly interacts with the CD38 regulatory region. Furthermore, E2A binding was stronger in the presence of the G allele. Experiments of E2A silencing led to a significant reduction of surface levels of CD38, confirming the working hypothesis. A direct functional interplay between E2A and CD38 was shown by exposing CLL cells to interleukin-2 and TLR-9 ligands, both inducers of CD38 expression. Under these conditions, CD38 upregulation was primarily conditioned by the presence of E2A and then by the G allele. The results of this study link E2A and CD38 expression within a common pathway, in which E-protein activity is required for the efficient induction of CD38 transcription.
AB - CD38, a nucleotide-metabolizing ectoenzyme and a receptor, is a negative prognostic marker for chronic lymphocytic leukemia (CLL) patients. CD38 has a genetic polymorphism, with a C G variation in a putative E-box located in a regulatory region. E2A, the predominant E-box factor in B lymphocytes, was found to be highly expressed by CD38 CLL patients. The highest CD38 levels scored by E2A /G carrier patients suggested that E2A is (i) directly associated with CD38 expression, and that (ii) the binding of the transcription factor is influenced by the CD38 genotype. Chromatin immunoprecipitation indicated that E2A directly interacts with the CD38 regulatory region. Furthermore, E2A binding was stronger in the presence of the G allele. Experiments of E2A silencing led to a significant reduction of surface levels of CD38, confirming the working hypothesis. A direct functional interplay between E2A and CD38 was shown by exposing CLL cells to interleukin-2 and TLR-9 ligands, both inducers of CD38 expression. Under these conditions, CD38 upregulation was primarily conditioned by the presence of E2A and then by the G allele. The results of this study link E2A and CD38 expression within a common pathway, in which E-protein activity is required for the efficient induction of CD38 transcription.
KW - CD38
KW - E2A
KW - SNP
KW - chronic lymphocytic leukemia
KW - transcriptional regulation
UR - http://www.scopus.com/inward/record.url?scp=79952445314&partnerID=8YFLogxK
U2 - 10.1038/leu.2010.291
DO - 10.1038/leu.2010.291
M3 - Article
SN - 0887-6924
VL - 25
SP - 479
EP - 488
JO - Leukemia
JF - Leukemia
IS - 3
ER -