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Overexpression of NSUN2 by DNA hypomethylation is associated with metastatic progression in human breast cancer

NSUN2 is a RNA methyltransferase that has been shown to be implicated in development of human cancer. However, the functional role of NSUN2, mechanism of NSUN2 overexpression and its association with clinicopathologic features in breast cancer remain unclear. To investigate alterations in the expres...

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Autores principales: Yi, Jie, Gao, Ran, Chen, Yu, Yang, Zhuo, Han, Pei, Zhang, Hui, Dou, Yaling, Liu, Wenjing, Wang, Wengong, Du, Guanhua, Xu, Yingchun, Wang, Jinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400542/
https://www.ncbi.nlm.nih.gov/pubmed/27447970
http://dx.doi.org/10.18632/oncotarget.10612
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author Yi, Jie
Gao, Ran
Chen, Yu
Yang, Zhuo
Han, Pei
Zhang, Hui
Dou, Yaling
Liu, Wenjing
Wang, Wengong
Du, Guanhua
Xu, Yingchun
Wang, Jinhua
author_facet Yi, Jie
Gao, Ran
Chen, Yu
Yang, Zhuo
Han, Pei
Zhang, Hui
Dou, Yaling
Liu, Wenjing
Wang, Wengong
Du, Guanhua
Xu, Yingchun
Wang, Jinhua
author_sort Yi, Jie
collection PubMed
description NSUN2 is a RNA methyltransferase that has been shown to be implicated in development of human cancer. However, the functional role of NSUN2, mechanism of NSUN2 overexpression and its association with clinicopathologic features in breast cancer remain unclear. To investigate alterations in the expression and functional role of NSUN2 in breast cancer, NSUN2 expression was assessed in breast cancer cells and tissues obtained from cancers at different American Joint Committee on Cancer (AJCC) stages, and its functions were investigated using breast cancer cells. NSUN2 expression was shown to be significantly higher in breast cancer cells and tissues than in normal breast epithelial cells and tissues, at both mRNA and protein levels. Overexpression of NSUN2 was shown to promote cell proliferation, migration, and invasion while NSUN2 knockdown inhibited these processes in vitro and in vivo. NSUN2 expression level was associated with the methylation level of its promoter. Our results demonstrated that the overall expression of NSUN2 significantly correlated with clinical stage (P=0.027), tumor classification (P=0.012), pathological differentiation (P=0.023), as well as with the expression levels of estrogen receptor (P<0.001), progesterone receptor (P=0.001), and Ki-67 (P<0.001). Our findings provide a unique insight into the roles and effects of NSUN2 overexpression in breast cancer cells, and highlight the necessity of the investigation of novel therapeutic targets, such as NSUN2, for the improvement of breast cancer treatments.
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spelling pubmed-54005422017-05-03 Overexpression of NSUN2 by DNA hypomethylation is associated with metastatic progression in human breast cancer Yi, Jie Gao, Ran Chen, Yu Yang, Zhuo Han, Pei Zhang, Hui Dou, Yaling Liu, Wenjing Wang, Wengong Du, Guanhua Xu, Yingchun Wang, Jinhua Oncotarget Research Paper NSUN2 is a RNA methyltransferase that has been shown to be implicated in development of human cancer. However, the functional role of NSUN2, mechanism of NSUN2 overexpression and its association with clinicopathologic features in breast cancer remain unclear. To investigate alterations in the expression and functional role of NSUN2 in breast cancer, NSUN2 expression was assessed in breast cancer cells and tissues obtained from cancers at different American Joint Committee on Cancer (AJCC) stages, and its functions were investigated using breast cancer cells. NSUN2 expression was shown to be significantly higher in breast cancer cells and tissues than in normal breast epithelial cells and tissues, at both mRNA and protein levels. Overexpression of NSUN2 was shown to promote cell proliferation, migration, and invasion while NSUN2 knockdown inhibited these processes in vitro and in vivo. NSUN2 expression level was associated with the methylation level of its promoter. Our results demonstrated that the overall expression of NSUN2 significantly correlated with clinical stage (P=0.027), tumor classification (P=0.012), pathological differentiation (P=0.023), as well as with the expression levels of estrogen receptor (P<0.001), progesterone receptor (P=0.001), and Ki-67 (P<0.001). Our findings provide a unique insight into the roles and effects of NSUN2 overexpression in breast cancer cells, and highlight the necessity of the investigation of novel therapeutic targets, such as NSUN2, for the improvement of breast cancer treatments. Impact Journals LLC 2016-11-30 /pmc/articles/PMC5400542/ /pubmed/27447970 http://dx.doi.org/10.18632/oncotarget.10612 Text en Copyright: © 2017 Yi et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Yi, Jie
Gao, Ran
Chen, Yu
Yang, Zhuo
Han, Pei
Zhang, Hui
Dou, Yaling
Liu, Wenjing
Wang, Wengong
Du, Guanhua
Xu, Yingchun
Wang, Jinhua
Overexpression of NSUN2 by DNA hypomethylation is associated with metastatic progression in human breast cancer
title Overexpression of NSUN2 by DNA hypomethylation is associated with metastatic progression in human breast cancer
title_full Overexpression of NSUN2 by DNA hypomethylation is associated with metastatic progression in human breast cancer
title_fullStr Overexpression of NSUN2 by DNA hypomethylation is associated with metastatic progression in human breast cancer
title_full_unstemmed Overexpression of NSUN2 by DNA hypomethylation is associated with metastatic progression in human breast cancer
title_short Overexpression of NSUN2 by DNA hypomethylation is associated with metastatic progression in human breast cancer
title_sort overexpression of nsun2 by dna hypomethylation is associated with metastatic progression in human breast cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400542/
https://www.ncbi.nlm.nih.gov/pubmed/27447970
http://dx.doi.org/10.18632/oncotarget.10612
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