Cargando…
MEF2D在肺腺癌中的表达及与预后的相关性分析
Background and objective Myocyte enhancer factor 2D (MEF2D) can participate in the process of tumor lesions by regulating the transcription of oncogenes. In a previous study, MEF2D was demonstrated to enhance the proliferation and metastasis of lung adenocarcinoma cells A549 and H1299 by promoting t...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Editorial board of Chinese Journal of Lung Cancer
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476217/ https://www.ncbi.nlm.nih.gov/pubmed/37653017 http://dx.doi.org/10.3779/j.issn.1009-3419.2023.102.25 |
_version_ | 1785100880171761664 |
---|---|
author | YE, Guangbin ZHANG, Zhongwei LI, Yanli GAO, Li HUANG, Wei LING, Bo |
author_facet | YE, Guangbin ZHANG, Zhongwei LI, Yanli GAO, Li HUANG, Wei LING, Bo |
author_sort | YE, Guangbin |
collection | PubMed |
description | Background and objective Myocyte enhancer factor 2D (MEF2D) can participate in the process of tumor lesions by regulating the transcription of oncogenes. In a previous study, MEF2D was demonstrated to enhance the proliferation and metastasis of lung adenocarcinoma cells A549 and H1299 by promoting the transcription of NUSAP1. The research aimed to explore the expression level and clinical significance of MEF2D in lung adenocarcinoma. Methods A total of 199 patients with lung adenocarcinoma were collected. Immunohistochemical staining was used to detect MEF2D expression levels in cancer and adjacent tissues. After the clinical and follow-up data were collated, the correlation between MEF2D expression level and clinical characteristics and prognosis of the patients was analyzed. Results In the lung adenocarcinoma, the high expression rate of MEF2D in cancer tissues was significantly higher than that in adjacent tissues (P<0.05). According to immunohistochemical score, MEF2D expression level in lung adenocarcinoma tissues was correlated with tumor differentiation, N stage, M stage and intrapulmonary metastasis (P<0.05). Kaplan-Meier analysis showed that patients with low MEF2D expression had significantly better prognosis than patients with high MEF2D expression (P<0.05). Cox multivariate analysis showed that MEF2D expression level, M stage, N stage and bone metastasis of lung cancer were independent risk factors for prognosis of lung adenocarcinoma patients. Conclussion MEF2D expression level is closely related to the metastasis of lung adenocarcinoma and other clinical characteristics, and can be used as an independent risk factor for the prognosis of patients with lung adenocarcinoma, which has the potential to be developed as a clinical diagnosis and treatment target of lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-10476217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Editorial board of Chinese Journal of Lung Cancer |
record_format | MEDLINE/PubMed |
spelling | pubmed-104762172023-09-05 MEF2D在肺腺癌中的表达及与预后的相关性分析 YE, Guangbin ZHANG, Zhongwei LI, Yanli GAO, Li HUANG, Wei LING, Bo Zhongguo Fei Ai Za Zhi Clinical Research Background and objective Myocyte enhancer factor 2D (MEF2D) can participate in the process of tumor lesions by regulating the transcription of oncogenes. In a previous study, MEF2D was demonstrated to enhance the proliferation and metastasis of lung adenocarcinoma cells A549 and H1299 by promoting the transcription of NUSAP1. The research aimed to explore the expression level and clinical significance of MEF2D in lung adenocarcinoma. Methods A total of 199 patients with lung adenocarcinoma were collected. Immunohistochemical staining was used to detect MEF2D expression levels in cancer and adjacent tissues. After the clinical and follow-up data were collated, the correlation between MEF2D expression level and clinical characteristics and prognosis of the patients was analyzed. Results In the lung adenocarcinoma, the high expression rate of MEF2D in cancer tissues was significantly higher than that in adjacent tissues (P<0.05). According to immunohistochemical score, MEF2D expression level in lung adenocarcinoma tissues was correlated with tumor differentiation, N stage, M stage and intrapulmonary metastasis (P<0.05). Kaplan-Meier analysis showed that patients with low MEF2D expression had significantly better prognosis than patients with high MEF2D expression (P<0.05). Cox multivariate analysis showed that MEF2D expression level, M stage, N stage and bone metastasis of lung cancer were independent risk factors for prognosis of lung adenocarcinoma patients. Conclussion MEF2D expression level is closely related to the metastasis of lung adenocarcinoma and other clinical characteristics, and can be used as an independent risk factor for the prognosis of patients with lung adenocarcinoma, which has the potential to be developed as a clinical diagnosis and treatment target of lung adenocarcinoma. Editorial board of Chinese Journal of Lung Cancer 2023-07-20 /pmc/articles/PMC10476217/ /pubmed/37653017 http://dx.doi.org/10.3779/j.issn.1009-3419.2023.102.25 Text en 版权所有 © 2023《中国肺癌杂志》编辑部 https://creativecommons.org/licenses/by/3.0/This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/. |
spellingShingle | Clinical Research YE, Guangbin ZHANG, Zhongwei LI, Yanli GAO, Li HUANG, Wei LING, Bo MEF2D在肺腺癌中的表达及与预后的相关性分析 |
title | MEF2D在肺腺癌中的表达及与预后的相关性分析 |
title_full | MEF2D在肺腺癌中的表达及与预后的相关性分析 |
title_fullStr | MEF2D在肺腺癌中的表达及与预后的相关性分析 |
title_full_unstemmed | MEF2D在肺腺癌中的表达及与预后的相关性分析 |
title_short | MEF2D在肺腺癌中的表达及与预后的相关性分析 |
title_sort | mef2d在肺腺癌中的表达及与预后的相关性分析 |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476217/ https://www.ncbi.nlm.nih.gov/pubmed/37653017 http://dx.doi.org/10.3779/j.issn.1009-3419.2023.102.25 |
work_keys_str_mv | AT yeguangbin mef2dzàifèixiànáizhōngdebiǎodájíyǔyùhòudexiāngguānxìngfēnxī AT zhangzhongwei mef2dzàifèixiànáizhōngdebiǎodájíyǔyùhòudexiāngguānxìngfēnxī AT liyanli mef2dzàifèixiànáizhōngdebiǎodájíyǔyùhòudexiāngguānxìngfēnxī AT gaoli mef2dzàifèixiànáizhōngdebiǎodájíyǔyùhòudexiāngguānxìngfēnxī AT huangwei mef2dzàifèixiànáizhōngdebiǎodájíyǔyùhòudexiāngguānxìngfēnxī AT lingbo mef2dzàifèixiànáizhōngdebiǎodájíyǔyùhòudexiāngguānxìngfēnxī |