Increased SHISA3 expression characterizes chronic lymphocytic leukemia patients sensitive to lenalidomide

  • Rossana Maffei
  • , Stefania Fiorcari
  • , Silvia Martinelli
  • , Stefania Benatti
  • , Jenny Bulgarelli
  • , Lara Rizzotto
  • , Giulia Debbia
  • , Rita Santachiara
  • , Gian Matteo Rigolin
  • , Francesco Forconi
  • , Davide Rossi
  • , Luca Laurenti
  • , Giuseppe A. Palumbo
  • , Daniele Vallisa
  • , Antonio Cuneo
  • , Gianluca Gaidano
  • , Mario Luppi
  • , Roberto Marasca*
  • *Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivistaArticolo

3 Citazioni (Scopus)

Abstract

Lenalidomide is a therapeutically effective drug in chronic lymphocytic leukemia (CLL). Twenty-seven CLL patients were treated with lenalidomide in a phase II clinical trial. Ten patients were grouped as responders (R) and 6 as nonresponders (NR). We evaluated T lymphocytes, NK, monocytes and dendritic cells at baseline and after treatment. A gene expression analysis was performed on 16 CLL samples collected before treatment. The levels of immune cells or immune-related cytokines are not different between R and NR patients. However, CLL patients sensitive to lenalidomide clearly show a peculiar gene expression profile in leukemic cells. The most up-regulated gene (fold change = +23 in R vs. NR) is Wnt inhibitor SHISA homolog 3 (SHISA3). SHISA3highCLL are characterized by a restrained activation of Wnt signaling and sensibility to lenalidomide-induced apoptosis. In conclusion, SHISA3 is a candidate gene for the identification of CLL patients who will benefit of lenalidomide treatment as single agent.
Lingua originaleInglese
pagine (da-a)423-433
Numero di pagine11
RivistaLEUKEMIA & LYMPHOMA
Volume59
Numero di pubblicazione2
DOI
Stato di pubblicazionePubblicato - 2018

All Science Journal Classification (ASJC) codes

  • Ematologia
  • Oncologia
  • Ricerca sul Cancro

Keywords

  • Cancer Research
  • Chronic lymphocytic leukemia
  • Hematology
  • Oncology
  • SHISA3
  • Wnt signaling
  • clinical response
  • lenalidomide

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