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A 4‐gene expression score associated with high levels of Wilms Tumor‐1 (WT1) expression is an adverse prognostic factor in acute myeloid leukaemia

Wilms Tumor‐1 (WT1) expression level is implicated in the prognosis of acute myeloid leukaemia (AML). We hypothesized that a gene expression profile associated with WT1 expression levels might be a good surrogate marker. We identified high WT1 gene sets by comparing the gene expression profiles in t...

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Autores principales: Niavarani, Ahmadreza, Herold, Tobias, Reyal, Yasmin, Sauerland, Maria C., Buchner, Thomas, Hiddemann, Wolfgang, Bohlander, Stefan K., Valk, Peter J. M., Bonnet, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833185/
https://www.ncbi.nlm.nih.gov/pubmed/26597595
http://dx.doi.org/10.1111/bjh.13836
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author Niavarani, Ahmadreza
Herold, Tobias
Reyal, Yasmin
Sauerland, Maria C.
Buchner, Thomas
Hiddemann, Wolfgang
Bohlander, Stefan K.
Valk, Peter J. M.
Bonnet, Dominique
author_facet Niavarani, Ahmadreza
Herold, Tobias
Reyal, Yasmin
Sauerland, Maria C.
Buchner, Thomas
Hiddemann, Wolfgang
Bohlander, Stefan K.
Valk, Peter J. M.
Bonnet, Dominique
author_sort Niavarani, Ahmadreza
collection PubMed
description Wilms Tumor‐1 (WT1) expression level is implicated in the prognosis of acute myeloid leukaemia (AML). We hypothesized that a gene expression profile associated with WT1 expression levels might be a good surrogate marker. We identified high WT1 gene sets by comparing the gene expression profiles in the highest and lowest quartiles of WT1 expression in two large AML studies. Two high WT1 gene sets were found to be highly correlated in terms of the altered genes and expression profiles. We identified a 17‐probe set signature of the high WT1 set as the optimal prognostic predictor in the first AML set, and showed that it was able to predict prognosis in the second AML series after adjustment for European LeukaemiaNet genetic groups. The gene signature also proved to be of prognostic value in a third AML series of 163 samples assessed by RNA sequencing, demonstrating its cross‐platform consistency. This led us to derive a 4‐gene expression score, which faithfully predicted adverse outcome. In conclusion, a short gene signature associated with high WT1 expression levels and the resultant 4‐gene expression score were found to be predictive of adverse prognosis in AML. This study provides new clues to the molecular pathways underlying high WT1 states in leukaemia.
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spelling pubmed-48331852016-06-24 A 4‐gene expression score associated with high levels of Wilms Tumor‐1 (WT1) expression is an adverse prognostic factor in acute myeloid leukaemia Niavarani, Ahmadreza Herold, Tobias Reyal, Yasmin Sauerland, Maria C. Buchner, Thomas Hiddemann, Wolfgang Bohlander, Stefan K. Valk, Peter J. M. Bonnet, Dominique Br J Haematol Haematological Malignancy Wilms Tumor‐1 (WT1) expression level is implicated in the prognosis of acute myeloid leukaemia (AML). We hypothesized that a gene expression profile associated with WT1 expression levels might be a good surrogate marker. We identified high WT1 gene sets by comparing the gene expression profiles in the highest and lowest quartiles of WT1 expression in two large AML studies. Two high WT1 gene sets were found to be highly correlated in terms of the altered genes and expression profiles. We identified a 17‐probe set signature of the high WT1 set as the optimal prognostic predictor in the first AML set, and showed that it was able to predict prognosis in the second AML series after adjustment for European LeukaemiaNet genetic groups. The gene signature also proved to be of prognostic value in a third AML series of 163 samples assessed by RNA sequencing, demonstrating its cross‐platform consistency. This led us to derive a 4‐gene expression score, which faithfully predicted adverse outcome. In conclusion, a short gene signature associated with high WT1 expression levels and the resultant 4‐gene expression score were found to be predictive of adverse prognosis in AML. This study provides new clues to the molecular pathways underlying high WT1 states in leukaemia. John Wiley and Sons Inc. 2016-02 2015-11-24 /pmc/articles/PMC4833185/ /pubmed/26597595 http://dx.doi.org/10.1111/bjh.13836 Text en © 2015 The Authors. British Journal of Haematology published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Haematological Malignancy
Niavarani, Ahmadreza
Herold, Tobias
Reyal, Yasmin
Sauerland, Maria C.
Buchner, Thomas
Hiddemann, Wolfgang
Bohlander, Stefan K.
Valk, Peter J. M.
Bonnet, Dominique
A 4‐gene expression score associated with high levels of Wilms Tumor‐1 (WT1) expression is an adverse prognostic factor in acute myeloid leukaemia
title A 4‐gene expression score associated with high levels of Wilms Tumor‐1 (WT1) expression is an adverse prognostic factor in acute myeloid leukaemia
title_full A 4‐gene expression score associated with high levels of Wilms Tumor‐1 (WT1) expression is an adverse prognostic factor in acute myeloid leukaemia
title_fullStr A 4‐gene expression score associated with high levels of Wilms Tumor‐1 (WT1) expression is an adverse prognostic factor in acute myeloid leukaemia
title_full_unstemmed A 4‐gene expression score associated with high levels of Wilms Tumor‐1 (WT1) expression is an adverse prognostic factor in acute myeloid leukaemia
title_short A 4‐gene expression score associated with high levels of Wilms Tumor‐1 (WT1) expression is an adverse prognostic factor in acute myeloid leukaemia
title_sort 4‐gene expression score associated with high levels of wilms tumor‐1 (wt1) expression is an adverse prognostic factor in acute myeloid leukaemia
topic Haematological Malignancy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833185/
https://www.ncbi.nlm.nih.gov/pubmed/26597595
http://dx.doi.org/10.1111/bjh.13836
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