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Prognostic value of miR-96 in patients with acute myeloid leukemia

OBJECTIVE: Aberrant expression of miRNA (miR)-96 is associated with tumorigenesis and tumor progression in several solid cancers. However, little is known about the expression and prognostic value of miR-96 in acute myeloid leukemia (AML). Therefore, the aim of this study was to investigate the corr...

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Autores principales: Zhao, Jiangning, Lu, Quanyi, Zhu, Junfeng, Fu, Jianguo, Chen, Yun-xian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975266/
https://www.ncbi.nlm.nih.gov/pubmed/24678958
http://dx.doi.org/10.1186/1746-1596-9-76
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author Zhao, Jiangning
Lu, Quanyi
Zhu, Junfeng
Fu, Jianguo
Chen, Yun-xian
author_facet Zhao, Jiangning
Lu, Quanyi
Zhu, Junfeng
Fu, Jianguo
Chen, Yun-xian
author_sort Zhao, Jiangning
collection PubMed
description OBJECTIVE: Aberrant expression of miRNA (miR)-96 is associated with tumorigenesis and tumor progression in several solid cancers. However, little is known about the expression and prognostic value of miR-96 in acute myeloid leukemia (AML). Therefore, the aim of this study was to investigate the correlation of miR-96 expression with clinicopathological features and prognosis of AML. METHODS: Real-time quantitative RT-PCR assay was performed to evaluate the expression levels of miR-96 in mononuclear cells from bone marrow or peripheral blood specimens in 86 patients with newly diagnosed AML. RESULTS: Compared with normal controls, miR-96 expression was significantly downregulated in patients with newly diagnosed AML (P < 0.001). In analysis of 14 diagnosis/CR-paired samples, the expression level of miR-96 was found markedly elevated in patients after treatment than before (P < 0.001). Moreover, lower levels of miR-96 were associated with a higher white blood cell count, bone marrow blast count (P < 0.001 and 0.022, respectively), and lower hemoglobin and platelet count (P = 0.036 and 0.033, respectively). Although the low-expression group seemed to have a lower CR rate (53.85% vs 70.0%), there was no significant difference between the two groups (P = 0.213). The low-expression group had a lower relapse-free survival (RFS) (P = 0.038) and overall survival (OS) (P = 0.022) compared with the high-expression group during a median follow-up of 20 months. CONCLUSION: Our data demonstrated that the expression of miR-96 was downregulated in newly diagnosed AML patients and associated with leukemic burden, as well as RFS and OS. This suggests that miR-96 detection might become a potential biomarker of prognosis and monitoring in AML. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1434808553949498
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spelling pubmed-39752662014-04-05 Prognostic value of miR-96 in patients with acute myeloid leukemia Zhao, Jiangning Lu, Quanyi Zhu, Junfeng Fu, Jianguo Chen, Yun-xian Diagn Pathol Research OBJECTIVE: Aberrant expression of miRNA (miR)-96 is associated with tumorigenesis and tumor progression in several solid cancers. However, little is known about the expression and prognostic value of miR-96 in acute myeloid leukemia (AML). Therefore, the aim of this study was to investigate the correlation of miR-96 expression with clinicopathological features and prognosis of AML. METHODS: Real-time quantitative RT-PCR assay was performed to evaluate the expression levels of miR-96 in mononuclear cells from bone marrow or peripheral blood specimens in 86 patients with newly diagnosed AML. RESULTS: Compared with normal controls, miR-96 expression was significantly downregulated in patients with newly diagnosed AML (P < 0.001). In analysis of 14 diagnosis/CR-paired samples, the expression level of miR-96 was found markedly elevated in patients after treatment than before (P < 0.001). Moreover, lower levels of miR-96 were associated with a higher white blood cell count, bone marrow blast count (P < 0.001 and 0.022, respectively), and lower hemoglobin and platelet count (P = 0.036 and 0.033, respectively). Although the low-expression group seemed to have a lower CR rate (53.85% vs 70.0%), there was no significant difference between the two groups (P = 0.213). The low-expression group had a lower relapse-free survival (RFS) (P = 0.038) and overall survival (OS) (P = 0.022) compared with the high-expression group during a median follow-up of 20 months. CONCLUSION: Our data demonstrated that the expression of miR-96 was downregulated in newly diagnosed AML patients and associated with leukemic burden, as well as RFS and OS. This suggests that miR-96 detection might become a potential biomarker of prognosis and monitoring in AML. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1434808553949498 BioMed Central 2014-03-29 /pmc/articles/PMC3975266/ /pubmed/24678958 http://dx.doi.org/10.1186/1746-1596-9-76 Text en Copyright © 2014 Zhao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research
Zhao, Jiangning
Lu, Quanyi
Zhu, Junfeng
Fu, Jianguo
Chen, Yun-xian
Prognostic value of miR-96 in patients with acute myeloid leukemia
title Prognostic value of miR-96 in patients with acute myeloid leukemia
title_full Prognostic value of miR-96 in patients with acute myeloid leukemia
title_fullStr Prognostic value of miR-96 in patients with acute myeloid leukemia
title_full_unstemmed Prognostic value of miR-96 in patients with acute myeloid leukemia
title_short Prognostic value of miR-96 in patients with acute myeloid leukemia
title_sort prognostic value of mir-96 in patients with acute myeloid leukemia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975266/
https://www.ncbi.nlm.nih.gov/pubmed/24678958
http://dx.doi.org/10.1186/1746-1596-9-76
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