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High expression of MAP7 predicts adverse prognosis in young patients with cytogenetically normal acute myeloid leukemia
Microtubule-associated protein 7 (MAP7) plays an important role in cancer cells. In this study, we identified the prognostic significance of MAP7 expression in cytogenetically normal acute myeloid leukemia (CN-AML) patients (aged <60 years) based on several microarray datasets. In the first group...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043276/ https://www.ncbi.nlm.nih.gov/pubmed/27686215 http://dx.doi.org/10.1038/srep34546 |
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author | Fu, Lin Fu, Huaping Zhou, Lei Xu, Keman Pang, Yifan Hu, Kai Wang, Jing Tian, Lei Liu, Yuanyuan Wang, Jijun Jing, Hongmei Huang, Wenrong Ke, Xiaoyan Shi, Jinlong |
author_facet | Fu, Lin Fu, Huaping Zhou, Lei Xu, Keman Pang, Yifan Hu, Kai Wang, Jing Tian, Lei Liu, Yuanyuan Wang, Jijun Jing, Hongmei Huang, Wenrong Ke, Xiaoyan Shi, Jinlong |
author_sort | Fu, Lin |
collection | PubMed |
description | Microtubule-associated protein 7 (MAP7) plays an important role in cancer cells. In this study, we identified the prognostic significance of MAP7 expression in cytogenetically normal acute myeloid leukemia (CN-AML) patients (aged <60 years) based on several microarray datasets. In the first group (n = 129), high MAP7 expression (MAP7(high)) was associated with adverse overall survival (OS; P = 0.0441) and event-free survival (EFS; P = 0.0114) compared with low MAP7 expression (MAP7(low)). In addition, the prognostic significance of MAP7 was confirmed by European Leukemia Net (ELN) intermediate-I genetic categories and multivariable analysis. In the second independent group of CN-AML patients (aged <60 years), MAP7(high) was also associated with adverse OS (n = 88, OS; P = 0.00811). To understand the inherent mechanisms of MAP7’s prognosis, we investigated genome-wide gene/microRNA expression signatures associated with MAP7 expression. Several known oncogenic genes/microRNAs and anti-oncogenic genes/microRNAs were disordered in MAP7(high) CN-AML patients. In conclusion, MAP7(high) is an adverse prognostic biomarker for CN-AML, which may be attributed to the distinctive genome-wide gene/microRNA expression and related cell signaling pathways. |
format | Online Article Text |
id | pubmed-5043276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50432762016-10-05 High expression of MAP7 predicts adverse prognosis in young patients with cytogenetically normal acute myeloid leukemia Fu, Lin Fu, Huaping Zhou, Lei Xu, Keman Pang, Yifan Hu, Kai Wang, Jing Tian, Lei Liu, Yuanyuan Wang, Jijun Jing, Hongmei Huang, Wenrong Ke, Xiaoyan Shi, Jinlong Sci Rep Article Microtubule-associated protein 7 (MAP7) plays an important role in cancer cells. In this study, we identified the prognostic significance of MAP7 expression in cytogenetically normal acute myeloid leukemia (CN-AML) patients (aged <60 years) based on several microarray datasets. In the first group (n = 129), high MAP7 expression (MAP7(high)) was associated with adverse overall survival (OS; P = 0.0441) and event-free survival (EFS; P = 0.0114) compared with low MAP7 expression (MAP7(low)). In addition, the prognostic significance of MAP7 was confirmed by European Leukemia Net (ELN) intermediate-I genetic categories and multivariable analysis. In the second independent group of CN-AML patients (aged <60 years), MAP7(high) was also associated with adverse OS (n = 88, OS; P = 0.00811). To understand the inherent mechanisms of MAP7’s prognosis, we investigated genome-wide gene/microRNA expression signatures associated with MAP7 expression. Several known oncogenic genes/microRNAs and anti-oncogenic genes/microRNAs were disordered in MAP7(high) CN-AML patients. In conclusion, MAP7(high) is an adverse prognostic biomarker for CN-AML, which may be attributed to the distinctive genome-wide gene/microRNA expression and related cell signaling pathways. Nature Publishing Group 2016-09-30 /pmc/articles/PMC5043276/ /pubmed/27686215 http://dx.doi.org/10.1038/srep34546 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fu, Lin Fu, Huaping Zhou, Lei Xu, Keman Pang, Yifan Hu, Kai Wang, Jing Tian, Lei Liu, Yuanyuan Wang, Jijun Jing, Hongmei Huang, Wenrong Ke, Xiaoyan Shi, Jinlong High expression of MAP7 predicts adverse prognosis in young patients with cytogenetically normal acute myeloid leukemia |
title | High expression of MAP7 predicts adverse prognosis in young patients with cytogenetically normal acute myeloid leukemia |
title_full | High expression of MAP7 predicts adverse prognosis in young patients with cytogenetically normal acute myeloid leukemia |
title_fullStr | High expression of MAP7 predicts adverse prognosis in young patients with cytogenetically normal acute myeloid leukemia |
title_full_unstemmed | High expression of MAP7 predicts adverse prognosis in young patients with cytogenetically normal acute myeloid leukemia |
title_short | High expression of MAP7 predicts adverse prognosis in young patients with cytogenetically normal acute myeloid leukemia |
title_sort | high expression of map7 predicts adverse prognosis in young patients with cytogenetically normal acute myeloid leukemia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043276/ https://www.ncbi.nlm.nih.gov/pubmed/27686215 http://dx.doi.org/10.1038/srep34546 |
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