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

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...

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Veröffentlicht in:Blood 2014-04, Vol.123 (15), p.2412-2415
Hauptverfasser: Havelange, Violaine, Ranganathan, Parvathi, Geyer, Susan, Nicolet, Deedra, Huang, Xiaomeng, Yu, Xueyan, Volinia, Stefano, Kornblau, Steven M., Andreeff, Michael, Croce, Carlo M., Marcucci, Guido, Bloomfield, Clara D., Garzon, Ramiro
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Sprache:eng
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Zusammenfassung: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. •High miR-10 family expression levels in AML patients are associated with achieving complete remission to induction chemotherapy.•Functional experiments did not show any impact of miR-10a-5p in AML blast growth or survival at baseline conditions or after chemotherapy.
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2013-10-532374