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Implications of the miR-10 family in chemotherapy response of NPM1-mutated AML

  • Violaine Havelange
  • , Parvathi Ranganathan
  • , Susan Geyer
  • , Deedra Nicolet
  • , Xiaomeng Huang
  • , Xueyan Yu
  • , Stefano Volinia
  • , Steven M. Kornblau
  • , Michael Andreeff
  • , Carlo M. Croce
  • , Guido Marcucci
  • , Clara D. Bloomfield
  • , Ramiro Garzon

Research output: Contribution to journal › Article › peer-review

Abstract

Nucleophosmin-mutated acute myeloid leukemia (NPM1mut-AML) patients have a high rate of complete remission (CR) to induction chemotherapy. However, the mechanisms responsible for such effects are unknown. Because miR-10 family members are expressed at high levels in NPM1mut-AML, we evaluated whether these microRNAs could predict chemotherapy response in AML. We found that high baseline miR-10 family expression in 54 untreated cytogenetically heterogeneous AML patients was associated with achieving CR. However, when we included NPM1 mutation status in the multivariable model, there was a significant interaction effect between miR-10a-5p expression and NPM1 mutation status. Similar results were observed when using a second cohort of 183 cytogenetically normal older (age ≥ 60 years) AML patients. Loss- and gain-of-function experiments using miR-10a-5p in cell lines and primary blasts did not demonstrate any effect in apoptosis or cell proliferation at baseline or after chemotherapy. These data support a bystander role for the miR-10 family in NPM1mut-AML.

Original languageEnglish (US)
Pages (from-to)2412-2415
Number of pages4
JournalBlood
Volume123
Issue number15
DOIs
StatePublished - Apr 10 2014

ASJC Scopus subject areas

  • Biochemistry
  • Immunology
  • Hematology
  • Cell Biology

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