Biological and therapeutic implications of a unique subtype of NPM1 mutated AML

Arvind Singh Mer(University Health Network), Emily Heath(University Health Network), Seyed Ali Madani Tonekaboni(University Health Network), Nergiz Doğan(University Health Network), Sisira Kadambat Nair(University Health Network), Alex Murison(University Health Network), Laura García‐Prat(University Health Network), Liran I. Shlush(Weizmann Institute of Science), Rose Hurren(University Health Network), Véronique Voisin(University of Toronto), Gary D. Bader(University of Toronto), Corey Nislow(University of British Columbia), Mattias Rantalainen(Karolinska Institutet), Sören Lehmann(Karolinska Institutet), Mark Gower(Hospital for Sick Children), Cynthia J. Guidos(Hospital for Sick Children), Mathieu Lupien(Ontario Institute for Cancer Research), John E. Dick(University Health Network), Mark D. Minden(University Health Network), Aaron D. Schimmer(University Health Network), Benjamin Haibe‐Kains(Ontario Institute for Cancer Research)
Nature Communications
February 16, 2021
Cited by 44Open Access
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Abstract

In acute myeloid leukemia (AML), molecular heterogeneity across patients constitutes a major challenge for prognosis and therapy. AML with NPM1 mutation is a distinct genetic entity in the revised World Health Organization classification. However, differing patterns of co-mutation and response to therapy within this group necessitate further stratification. Here we report two distinct subtypes within NPM1 mutated AML patients, which we label as primitive and committed based on the respective presence or absence of a stem cell signature. Using gene expression (RNA-seq), epigenomic (ATAC-seq) and immunophenotyping (CyToF) analysis, we associate each subtype with specific molecular characteristics, disease differentiation state and patient survival. Using ex vivo drug sensitivity profiling, we show a differential drug response of the subtypes to specific kinase inhibitors, irrespective of the FLT3-ITD status. Differential drug responses of the primitive and committed subtype are validated in an independent AML cohort. Our results highlight heterogeneity among NPM1 mutated AML patient samples based on stemness and suggest that the addition of kinase inhibitors to the treatment of cases with the primitive signature, lacking FLT3-ITD, could have therapeutic benefit.


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