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High expression of miR-107 and miR-17 predicts poor prognosis and guides treatment selection in acute myeloid leukemia
BACKGROUND: The prognostic significance of miR-107 and miR-17 in patients with acute myeloid leukemia (AML) remains unclear. METHODS: A total of 173 patients with de novo AML from the Cancer Genome Atlas database were enrolled in this study and further divided into a chemotherapy group (98 cases) an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174997/ https://www.ncbi.nlm.nih.gov/pubmed/37180663 http://dx.doi.org/10.21037/tcr-22-2484 |
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author | Liu, Yue Cao, Yang Yang, Xiaojun Chen, Huijuan Yang, Haonan Liu, Yan Gu, Weiying |
author_facet | Liu, Yue Cao, Yang Yang, Xiaojun Chen, Huijuan Yang, Haonan Liu, Yan Gu, Weiying |
author_sort | Liu, Yue |
collection | PubMed |
description | BACKGROUND: The prognostic significance of miR-107 and miR-17 in patients with acute myeloid leukemia (AML) remains unclear. METHODS: A total of 173 patients with de novo AML from the Cancer Genome Atlas database were enrolled in this study and further divided into a chemotherapy group (98 cases) and an allogeneic hematopoietic stem cell transplantation (allo-HSCT) group (75 cases) according to their therapy regimen. RESULTS: In the chemotherapy cohort, high miR-107 or miR-17 expression was associated with poorer overall survival (OS) and event-free survival (EFS). On the other hand, there were no significant differences in OS and EFS between the high- and low-expression subgroups in the allo-HSCT group. Next, we stratified the total number of patients with AML into high- and low-expression groups according to the median expression levels of miR-107 or miR-17. In the high miR-107 or miR-17 expression group, patients treated with allo-HSCT had longer OS than those treated with chemotherapy. In the low miR-107 or miR-17 expression group, no significant differences in OS and EFS were observed between the two therapy subgroups. When patients were further clustered into three groups (both low miR-107 and low miR-17, either high miR-107 or high miR-17, and both high miR-107 and high miR-17), patients with both high miR-107 and high miR-17 expression had the worst OS and EFS of the entire group and of the chemotherapy group. On the other hand, there were no significant differences in OS and EFS among the three subgroups in the allo-HSCT group. Cox regression confirmed the concurrence of high expression of miR-107 and miR-17 might act as an independent prognostic factor for EFS and OS in the entire group and the chemotherapy group. Bioinformatics analysis showed differentially expressed genes (DEGs) associated with miR-107 and miR-17 expression were mainly enriched in multiple metabolic processes. CONCLUSIONS: The combination of miR-107 and miR-17 provides prognostic significance for patients with AML and should be considered in the clinical selection of the optimal treatment regimen when deciding between chemotherapy and allo-HSCT. |
format | Online Article Text |
id | pubmed-10174997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-101749972023-05-12 High expression of miR-107 and miR-17 predicts poor prognosis and guides treatment selection in acute myeloid leukemia Liu, Yue Cao, Yang Yang, Xiaojun Chen, Huijuan Yang, Haonan Liu, Yan Gu, Weiying Transl Cancer Res Original Article BACKGROUND: The prognostic significance of miR-107 and miR-17 in patients with acute myeloid leukemia (AML) remains unclear. METHODS: A total of 173 patients with de novo AML from the Cancer Genome Atlas database were enrolled in this study and further divided into a chemotherapy group (98 cases) and an allogeneic hematopoietic stem cell transplantation (allo-HSCT) group (75 cases) according to their therapy regimen. RESULTS: In the chemotherapy cohort, high miR-107 or miR-17 expression was associated with poorer overall survival (OS) and event-free survival (EFS). On the other hand, there were no significant differences in OS and EFS between the high- and low-expression subgroups in the allo-HSCT group. Next, we stratified the total number of patients with AML into high- and low-expression groups according to the median expression levels of miR-107 or miR-17. In the high miR-107 or miR-17 expression group, patients treated with allo-HSCT had longer OS than those treated with chemotherapy. In the low miR-107 or miR-17 expression group, no significant differences in OS and EFS were observed between the two therapy subgroups. When patients were further clustered into three groups (both low miR-107 and low miR-17, either high miR-107 or high miR-17, and both high miR-107 and high miR-17), patients with both high miR-107 and high miR-17 expression had the worst OS and EFS of the entire group and of the chemotherapy group. On the other hand, there were no significant differences in OS and EFS among the three subgroups in the allo-HSCT group. Cox regression confirmed the concurrence of high expression of miR-107 and miR-17 might act as an independent prognostic factor for EFS and OS in the entire group and the chemotherapy group. Bioinformatics analysis showed differentially expressed genes (DEGs) associated with miR-107 and miR-17 expression were mainly enriched in multiple metabolic processes. CONCLUSIONS: The combination of miR-107 and miR-17 provides prognostic significance for patients with AML and should be considered in the clinical selection of the optimal treatment regimen when deciding between chemotherapy and allo-HSCT. AME Publishing Company 2023-03-17 2023-04-28 /pmc/articles/PMC10174997/ /pubmed/37180663 http://dx.doi.org/10.21037/tcr-22-2484 Text en 2023 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Liu, Yue Cao, Yang Yang, Xiaojun Chen, Huijuan Yang, Haonan Liu, Yan Gu, Weiying High expression of miR-107 and miR-17 predicts poor prognosis and guides treatment selection in acute myeloid leukemia |
title | High expression of miR-107 and miR-17 predicts poor prognosis and guides treatment selection in acute myeloid leukemia |
title_full | High expression of miR-107 and miR-17 predicts poor prognosis and guides treatment selection in acute myeloid leukemia |
title_fullStr | High expression of miR-107 and miR-17 predicts poor prognosis and guides treatment selection in acute myeloid leukemia |
title_full_unstemmed | High expression of miR-107 and miR-17 predicts poor prognosis and guides treatment selection in acute myeloid leukemia |
title_short | High expression of miR-107 and miR-17 predicts poor prognosis and guides treatment selection in acute myeloid leukemia |
title_sort | high expression of mir-107 and mir-17 predicts poor prognosis and guides treatment selection in acute myeloid leukemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174997/ https://www.ncbi.nlm.nih.gov/pubmed/37180663 http://dx.doi.org/10.21037/tcr-22-2484 |
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