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Validation of flow cytometric phospho-STAT5 as a diagnostic tool for juvenile myelomonocytic leukemia

To diagnose juvenile myelomonocytic leukemia (JMML) is sometimes challenging, because around 10% of patients lack molecular abnormalities affecting Ras-MAPK (mitogen-activated protein kinase) pathway and other diseases such as cytomegalovirus infection can mimic clinical signs of JMML. In order to v...

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Autores principales: Hasegawa, D, Bugarin, C, Giordan, M, Bresolin, S, Longoni, D, Micalizzi, C, Ramenghi, U, Bertaina, A, Basso, G, Locatelli, F, Biondi, A, te Kronnie, G, Gaipa, G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880439/
https://www.ncbi.nlm.nih.gov/pubmed/24241400
http://dx.doi.org/10.1038/bcj.2013.56
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author Hasegawa, D
Bugarin, C
Giordan, M
Bresolin, S
Longoni, D
Micalizzi, C
Ramenghi, U
Bertaina, A
Basso, G
Locatelli, F
Biondi, A
te Kronnie, G
Gaipa, G
author_facet Hasegawa, D
Bugarin, C
Giordan, M
Bresolin, S
Longoni, D
Micalizzi, C
Ramenghi, U
Bertaina, A
Basso, G
Locatelli, F
Biondi, A
te Kronnie, G
Gaipa, G
author_sort Hasegawa, D
collection PubMed
description To diagnose juvenile myelomonocytic leukemia (JMML) is sometimes challenging, because around 10% of patients lack molecular abnormalities affecting Ras-MAPK (mitogen-activated protein kinase) pathway and other diseases such as cytomegalovirus infection can mimic clinical signs of JMML. In order to validate a phospho-specific flow cytometry assay assessing phospho-signal transducer and activator of transcription factor 5 (p-STAT5) as a new diagnostic tool for JMML, we examined 22 samples from children with JMML and 47 controls. CD33+/CD34+ cells from 22 patients with JMML showed hyperphosphorylation of STAT5 induced by sub-saturating doses of granulocyte-macrophage colony-stimulating factor (GM-CSF). Using a training set of samples (11 JMML and 23 controls), we identified a threshold for p-STAT5-positive after stimulation with 0.1 ng/ml GM-CSF (17.17%) that discriminates JMML from controls. This threshold was validated in an independent series (11 JMML, 24 controls and 7 cases with diseases other than JMML) where we demonstrated that patients with JMML could be distinguished from other subjects with a sensitivity of 91% (confidence interval (CI) 59–100%) and a specificity of 87% (CI 70–96%). Positive and negative predictive values were 71% (CI 42–92%) and 96% (CI 82–100%), respectively. In conclusion, flow cytometric p-STAT5 profiling is a reliable diagnostic tool for identifying patients with JMML and can contribute to consistency of current diagnostic criteria.
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spelling pubmed-38804392014-01-04 Validation of flow cytometric phospho-STAT5 as a diagnostic tool for juvenile myelomonocytic leukemia Hasegawa, D Bugarin, C Giordan, M Bresolin, S Longoni, D Micalizzi, C Ramenghi, U Bertaina, A Basso, G Locatelli, F Biondi, A te Kronnie, G Gaipa, G Blood Cancer J Original Article To diagnose juvenile myelomonocytic leukemia (JMML) is sometimes challenging, because around 10% of patients lack molecular abnormalities affecting Ras-MAPK (mitogen-activated protein kinase) pathway and other diseases such as cytomegalovirus infection can mimic clinical signs of JMML. In order to validate a phospho-specific flow cytometry assay assessing phospho-signal transducer and activator of transcription factor 5 (p-STAT5) as a new diagnostic tool for JMML, we examined 22 samples from children with JMML and 47 controls. CD33+/CD34+ cells from 22 patients with JMML showed hyperphosphorylation of STAT5 induced by sub-saturating doses of granulocyte-macrophage colony-stimulating factor (GM-CSF). Using a training set of samples (11 JMML and 23 controls), we identified a threshold for p-STAT5-positive after stimulation with 0.1 ng/ml GM-CSF (17.17%) that discriminates JMML from controls. This threshold was validated in an independent series (11 JMML, 24 controls and 7 cases with diseases other than JMML) where we demonstrated that patients with JMML could be distinguished from other subjects with a sensitivity of 91% (confidence interval (CI) 59–100%) and a specificity of 87% (CI 70–96%). Positive and negative predictive values were 71% (CI 42–92%) and 96% (CI 82–100%), respectively. In conclusion, flow cytometric p-STAT5 profiling is a reliable diagnostic tool for identifying patients with JMML and can contribute to consistency of current diagnostic criteria. Nature Publishing Group 2013-11 2013-11-15 /pmc/articles/PMC3880439/ /pubmed/24241400 http://dx.doi.org/10.1038/bcj.2013.56 Text en Copyright © 2013 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Hasegawa, D
Bugarin, C
Giordan, M
Bresolin, S
Longoni, D
Micalizzi, C
Ramenghi, U
Bertaina, A
Basso, G
Locatelli, F
Biondi, A
te Kronnie, G
Gaipa, G
Validation of flow cytometric phospho-STAT5 as a diagnostic tool for juvenile myelomonocytic leukemia
title Validation of flow cytometric phospho-STAT5 as a diagnostic tool for juvenile myelomonocytic leukemia
title_full Validation of flow cytometric phospho-STAT5 as a diagnostic tool for juvenile myelomonocytic leukemia
title_fullStr Validation of flow cytometric phospho-STAT5 as a diagnostic tool for juvenile myelomonocytic leukemia
title_full_unstemmed Validation of flow cytometric phospho-STAT5 as a diagnostic tool for juvenile myelomonocytic leukemia
title_short Validation of flow cytometric phospho-STAT5 as a diagnostic tool for juvenile myelomonocytic leukemia
title_sort validation of flow cytometric phospho-stat5 as a diagnostic tool for juvenile myelomonocytic leukemia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3880439/
https://www.ncbi.nlm.nih.gov/pubmed/24241400
http://dx.doi.org/10.1038/bcj.2013.56
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