Oncogenic NRAS Primes Primary Acute Myeloid Leukemia Cells for Differentiation.

RAS mutations are frequently found among acute myeloid leukemia patients (AML), generating a constitutively active signaling protein changing cellular proliferation, differentiation and apoptosis. We have previously shown that treatment of AML patients with high-dose cytarabine is preferentially ben...

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Main Authors: Cornelia Brendel, Sabine Teichler, Axel Millahn, Thorsten Stiewe, Michael Krause, Kathleen Stabla, Petra Ross, Minh Huynh, Thomas Illmer, Marco Mernberger, Christina Barckhausen, Andreas Neubauer
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4406710?pdf=render
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spelling doaj-ca5657a754f64fcba645922ceb1ef2482020-11-25T02:29:40ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01104e012318110.1371/journal.pone.0123181Oncogenic NRAS Primes Primary Acute Myeloid Leukemia Cells for Differentiation.Cornelia BrendelSabine TeichlerAxel MillahnThorsten StieweMichael KrauseKathleen StablaPetra RossMinh HuynhThomas IllmerMarco MernbergerChristina BarckhausenAndreas NeubauerRAS mutations are frequently found among acute myeloid leukemia patients (AML), generating a constitutively active signaling protein changing cellular proliferation, differentiation and apoptosis. We have previously shown that treatment of AML patients with high-dose cytarabine is preferentially beneficial for those harboring oncogenic RAS. On the basis of a murine AML cell culture model, we ascribed this effect to a RAS-driven, p53-dependent induction of differentiation. Hence, in this study we sought to confirm the correlation between RAS status and differentiation of primary blasts obtained from AML patients. The gene expression signature of AML blasts with oncogenic NRAS indeed corresponded to a more mature profile compared to blasts with wildtype RAS, as demonstrated by gene set enrichment analysis (GSEA) and real-time PCR analysis of myeloid ecotropic viral integration site 1 homolog (MEIS1) in a unique cohort of AML patients. In addition, in vitro cell culture experiments with established cell lines and a second set of primary AML cells showed that oncogenic NRAS mutations predisposed cells to cytarabine (AraC) driven differentiation. Taken together, our findings show that AML with inv(16) and NRAS mutation have a differentiation gene signature, supporting the notion that NRAS mutation may predispose leukemic cells to AraC induced differentiation. We therefore suggest that promotion of differentiation pathways by specific genetic alterations could explain the superior treatment outcome after therapy in some AML patient subgroups. Whether a differentiation gene expression status may generally predict for a superior treatment outcome in AML needs to be addressed in future studies.http://europepmc.org/articles/PMC4406710?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Cornelia Brendel
Sabine Teichler
Axel Millahn
Thorsten Stiewe
Michael Krause
Kathleen Stabla
Petra Ross
Minh Huynh
Thomas Illmer
Marco Mernberger
Christina Barckhausen
Andreas Neubauer
spellingShingle Cornelia Brendel
Sabine Teichler
Axel Millahn
Thorsten Stiewe
Michael Krause
Kathleen Stabla
Petra Ross
Minh Huynh
Thomas Illmer
Marco Mernberger
Christina Barckhausen
Andreas Neubauer
Oncogenic NRAS Primes Primary Acute Myeloid Leukemia Cells for Differentiation.
PLoS ONE
author_facet Cornelia Brendel
Sabine Teichler
Axel Millahn
Thorsten Stiewe
Michael Krause
Kathleen Stabla
Petra Ross
Minh Huynh
Thomas Illmer
Marco Mernberger
Christina Barckhausen
Andreas Neubauer
author_sort Cornelia Brendel
title Oncogenic NRAS Primes Primary Acute Myeloid Leukemia Cells for Differentiation.
title_short Oncogenic NRAS Primes Primary Acute Myeloid Leukemia Cells for Differentiation.
title_full Oncogenic NRAS Primes Primary Acute Myeloid Leukemia Cells for Differentiation.
title_fullStr Oncogenic NRAS Primes Primary Acute Myeloid Leukemia Cells for Differentiation.
title_full_unstemmed Oncogenic NRAS Primes Primary Acute Myeloid Leukemia Cells for Differentiation.
title_sort oncogenic nras primes primary acute myeloid leukemia cells for differentiation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description RAS mutations are frequently found among acute myeloid leukemia patients (AML), generating a constitutively active signaling protein changing cellular proliferation, differentiation and apoptosis. We have previously shown that treatment of AML patients with high-dose cytarabine is preferentially beneficial for those harboring oncogenic RAS. On the basis of a murine AML cell culture model, we ascribed this effect to a RAS-driven, p53-dependent induction of differentiation. Hence, in this study we sought to confirm the correlation between RAS status and differentiation of primary blasts obtained from AML patients. The gene expression signature of AML blasts with oncogenic NRAS indeed corresponded to a more mature profile compared to blasts with wildtype RAS, as demonstrated by gene set enrichment analysis (GSEA) and real-time PCR analysis of myeloid ecotropic viral integration site 1 homolog (MEIS1) in a unique cohort of AML patients. In addition, in vitro cell culture experiments with established cell lines and a second set of primary AML cells showed that oncogenic NRAS mutations predisposed cells to cytarabine (AraC) driven differentiation. Taken together, our findings show that AML with inv(16) and NRAS mutation have a differentiation gene signature, supporting the notion that NRAS mutation may predispose leukemic cells to AraC induced differentiation. We therefore suggest that promotion of differentiation pathways by specific genetic alterations could explain the superior treatment outcome after therapy in some AML patient subgroups. Whether a differentiation gene expression status may generally predict for a superior treatment outcome in AML needs to be addressed in future studies.
url http://europepmc.org/articles/PMC4406710?pdf=render
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