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Oncotarget. 2017 Jul 22;8(35):59235-59245. doi: 10.18632/oncotarget.19494. eCollection 2017 Aug 29.

The γ-secretase inhibitors enhance the anti-leukemic activity of ibrutinib in B-CLL cells.

Oncotarget

Paola Secchiero, Rebecca Voltan, Erika Rimondi, Elisabetta Melloni, Emmanouil Athanasakis, Veronica Tisato, Stefania Gallo, Gian Matteo Rigolin, Giorgio Zauli

Affiliations

  1. Department of Morphology, Surgery and Experimental Medicine and LTTA Centre, University of Ferrara, Ferrara, Italy.
  2. Institute for Maternal and Child Health, IRCCS "Burlo Garofolo", Trieste, Italy.
  3. Department of Medical Sciences, Section of Hematology, University of Ferrara, Ferrara, Italy.

PMID: 28938632 PMCID: PMC5601728 DOI: 10.18632/oncotarget.19494

Abstract

Ibrutinib blocks B-cell receptor signaling and interferes with leukemic cell-to-microenvironment interactions. Ibrutinib plays a key role in the management of B-CLL and is recommended for first line treatment of high-risk CLL patients with 17p deletion. Therefore, elucidating the factors governing sensitivity/resistance to Ibrutinib represents a relevant issue. For this purpose, in 3 B-CLL patient samples harboring functional

Keywords: B-leukemic cells; Ibrutinib; NOTCH1; combination therapy; γ-secretase inhibitors

Conflict of interest statement

CONFLICTS OF INTEREST The authors declare no conflicts of interest.

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