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Expression of the miR-148/152 Family in Acute Myeloid Leukemia and its Clinical Significance

BACKGROUND: MicroRNAs (miRNAs) play an important role in the development and progression of acute myeloid leukemia (AML). The miR-148/152 family has been reported to be express differently in various kinds of tumors. We investigated the expression level of the miR-148/152 family in AML patients and...

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Autores principales: Wang, Xiao-Xue, Zhang, Rui, Li, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639952/
https://www.ncbi.nlm.nih.gov/pubmed/28978904
http://dx.doi.org/10.12659/MSM.902689
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author Wang, Xiao-Xue
Zhang, Rui
Li, Yan
author_facet Wang, Xiao-Xue
Zhang, Rui
Li, Yan
author_sort Wang, Xiao-Xue
collection PubMed
description BACKGROUND: MicroRNAs (miRNAs) play an important role in the development and progression of acute myeloid leukemia (AML). The miR-148/152 family has been reported to be express differently in various kinds of tumors. We investigated the expression level of the miR-148/152 family in AML patients and their clinical significance. MATERIAL/METHODS: Expression levels of the miR-148/152 family in 80 patients with newly diagnosed AML and 20 healthy participants were analyzed by qRT-PCR. We also evaluated the relationship between the expression levels of the miR-148/152 family and clinicopathological features of AML patients. RESULTS: Compared with healthy controls, we found a significant lower expression of downregulated miR-148/152 in AML patients (p<0.0001). The expression of miR148/152 family was associated with various AML clinicopathological risk parameters including FAB classifications, cytogenetics, and gene mutations. The number of patients with high expression levels of miR-148a/b was significantly increased in the low-risk group and significantly decreased in the high-risk group. (p=0.025, p=0.000, respectively). Patients with higher expression of miR-148b showed a higher complete remission (CR) rate (p=0.043). Importantly, higher expression of miR-148a/b was correlated with lower relapse rate (p=0.035, p=0.027, respectively) and showed a longer relapse-free survival (RFS) (p=0.0321, p=0.002, respectively). In the subgroup analysis, RFS was significantly affected by the expression of miR-148a/b in patients the high and the intermediate-risk groups (p=0.0499, p=0.0114, respectively). CONCLUSIONS: The expression levels of the miR-148/152 family were lower in patients with AML compared to healthy controls, and were associated with various AML clinicopathological parameters and therapeutic effect. The miR-148/152 family may prove to be a new biomarker for AML.
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spelling pubmed-56399522017-10-20 Expression of the miR-148/152 Family in Acute Myeloid Leukemia and its Clinical Significance Wang, Xiao-Xue Zhang, Rui Li, Yan Med Sci Monit Lab/In Vitro Research BACKGROUND: MicroRNAs (miRNAs) play an important role in the development and progression of acute myeloid leukemia (AML). The miR-148/152 family has been reported to be express differently in various kinds of tumors. We investigated the expression level of the miR-148/152 family in AML patients and their clinical significance. MATERIAL/METHODS: Expression levels of the miR-148/152 family in 80 patients with newly diagnosed AML and 20 healthy participants were analyzed by qRT-PCR. We also evaluated the relationship between the expression levels of the miR-148/152 family and clinicopathological features of AML patients. RESULTS: Compared with healthy controls, we found a significant lower expression of downregulated miR-148/152 in AML patients (p<0.0001). The expression of miR148/152 family was associated with various AML clinicopathological risk parameters including FAB classifications, cytogenetics, and gene mutations. The number of patients with high expression levels of miR-148a/b was significantly increased in the low-risk group and significantly decreased in the high-risk group. (p=0.025, p=0.000, respectively). Patients with higher expression of miR-148b showed a higher complete remission (CR) rate (p=0.043). Importantly, higher expression of miR-148a/b was correlated with lower relapse rate (p=0.035, p=0.027, respectively) and showed a longer relapse-free survival (RFS) (p=0.0321, p=0.002, respectively). In the subgroup analysis, RFS was significantly affected by the expression of miR-148a/b in patients the high and the intermediate-risk groups (p=0.0499, p=0.0114, respectively). CONCLUSIONS: The expression levels of the miR-148/152 family were lower in patients with AML compared to healthy controls, and were associated with various AML clinicopathological parameters and therapeutic effect. The miR-148/152 family may prove to be a new biomarker for AML. International Scientific Literature, Inc. 2017-10-05 /pmc/articles/PMC5639952/ /pubmed/28978904 http://dx.doi.org/10.12659/MSM.902689 Text en © Med Sci Monit, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Lab/In Vitro Research
Wang, Xiao-Xue
Zhang, Rui
Li, Yan
Expression of the miR-148/152 Family in Acute Myeloid Leukemia and its Clinical Significance
title Expression of the miR-148/152 Family in Acute Myeloid Leukemia and its Clinical Significance
title_full Expression of the miR-148/152 Family in Acute Myeloid Leukemia and its Clinical Significance
title_fullStr Expression of the miR-148/152 Family in Acute Myeloid Leukemia and its Clinical Significance
title_full_unstemmed Expression of the miR-148/152 Family in Acute Myeloid Leukemia and its Clinical Significance
title_short Expression of the miR-148/152 Family in Acute Myeloid Leukemia and its Clinical Significance
title_sort expression of the mir-148/152 family in acute myeloid leukemia and its clinical significance
topic Lab/In Vitro Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5639952/
https://www.ncbi.nlm.nih.gov/pubmed/28978904
http://dx.doi.org/10.12659/MSM.902689
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