NOTCH1 mutations are associated with high CD49d expression in chronic lymphocytic leukemia: Link between the NOTCH1 and the NF-κ B pathways

  • D. Benedetti
  • , E. Tissino
  • , F. Pozzo
  • , T. Bittolo
  • , C. Caldana
  • , C. Perini
  • , D. Martorelli
  • , V. Bravin
  • , T. D'Agaro
  • , F. M. Rossi
  • , R. Bomben
  • , E. Santinelli
  • , F. Zaja
  • , G. Pozzato
  • , A. Chiarenza
  • , F. Di Raimondo
  • , G. Del Poeta
  • , D. Rossi
  • , G. Gaidano
  • , M. Dal Bo
  • V. Gattei, A. Zucchetto

Risultato della ricerca: Contributo su rivistaArticolo in rivistapeer review

Abstract

In chronic lymphocytic leukemia (CLL), stabilizing mutations of NOTCH1, affecting up to 10-15% of cases, have been associated to poor prognosis, disease progression and refractoriness to chemotherapy. NOTCH1 mutations are significantly overrepresented in trisomy 12 CLL, a disease subset frequently expressing CD49d, the α4 chain of the very-late-activation-4 integrin, a well-known key regulator of microenviromental interactions, and negative prognosticator in CLL. In the present study, by analysing a wide cohort of 1180 CLL, we observed a very strong association between the presence of NOTCH1 mutations and the expression of CD49d (P<0.0001), occurring also outside the trisomy 12 CLL subset. Using both the MEC-1 CLL-like cells stably transfected with the NOTCH1 intracellular domain and primary CLL cells bearing a mutated or wild-type NOTCH1 gene configuration, we provide evidence that triggering of the NOTCH1 pathway resulted in a positive CD49d expression regulation, which was driven by a NOTCH1-dependent activation of nuclear factot-κ B (NF-κ B). Consistently, pharmacological inhibition of the NOTCH1 and/or of the NF-κ B pathways resulted in impaired NF-κ B nuclear translocation with consequent down-modulation of CD49d expression. Altogether, our data link for the first time NOTCH1 mutations to CD49d expression regulation through the involvement of the NF-κ B pathway in CLL.

Lingua originaleInglese
pagine (da-a)654-662
Numero di pagine9
RivistaLeukemia
Volume32
Numero di pubblicazione3
DOI
Stato di pubblicazionePubblicato - 1 mar 2018

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