Pim kinases modulate resistance to FLT3 tyrosine kinase inhibitors in FLT3-ITD acute myeloid leukemia

نویسندگان

  • Alexa S. Green
  • Thiago T. Maciel
  • Marie-Anne Hospital
  • Chae Yin
  • Fetta Mazed
  • Elizabeth C. Townsend
  • Sylvain Pilorge
  • Mireille Lambert
  • Etienne Paubelle
  • Arnaud Jacquel
  • Florence Zylbersztejn
  • Justine Decroocq
  • Laury Poulain
  • Pierre Sujobert
  • Nathalie Jacque
  • Kevin Adam
  • Jason C. C. So
  • Olivier Kosmider
  • Patrick Auberger
  • Olivier Hermine
  • David M. Weinstock
  • Catherine Lacombe
  • Patrick Mayeux
  • Gary J. Vanasse
  • Anskar Y. Leung
  • Ivan C. Moura
  • Didier Bouscary
  • Jerome Tamburini
چکیده

Fms-like tyrosine kinase 3 internal tandem duplication (FLT3-ITD) is frequently detected in acute myeloid leukemia (AML) patients and is associated with a dismal long-term prognosis. FLT3 tyrosine kinase inhibitors provide short-term disease control, but relapse invariably occurs within months. Pim protein kinases are oncogenic FLT3-ITD targets expressed in AML cells. We show that increased Pim kinase expression is found in relapse samples from AML patients treated with FLT3 inhibitors. Ectopic Pim-2 expression induces resistance to FLT3 inhibition in both FLT3-ITD-induced myeloproliferative neoplasm and AML models in mice. Strikingly, we found that Pim kinases govern FLT3-ITD signaling and that their pharmacological or genetic inhibition restores cell sensitivity to FLT3 inhibitors. Finally, dual inhibition of FLT3 and Pim kinases eradicates FLT3-ITD(+) cells including primary AML cells. Concomitant Pim and FLT3 inhibition represents a promising new avenue for AML therapy.

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عنوان ژورنال:

دوره 1  شماره 

صفحات  -

تاریخ انتشار 2015