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High expression of MAGE-A9 correlates with unfavorable survival in hepatocellular carcinoma

Melanoma-associated antigens (MAGE)-A9 has been reported to play important roles in the development of human cancers. However, the association between MAGE-A9 expression and the clinicopathological characteristics of hepatocellular carcinoma (HCC) is not well understood. The study was to detect the...

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Autores principales: Gu, Xuefeng, Fu, Maoying, Ge, Zhijun, Zhan, Feng, Ding, Yuqin, Ni, Huihui, Zhang, Wei, Zhu, Yanfang, Tang, Xiaojun, Xiong, Lin, Li, Jiang, Qiu, Liang, Mao, Yuan, Zhu, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197415/
https://www.ncbi.nlm.nih.gov/pubmed/25315972
http://dx.doi.org/10.1038/srep06625
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author Gu, Xuefeng
Fu, Maoying
Ge, Zhijun
Zhan, Feng
Ding, Yuqin
Ni, Huihui
Zhang, Wei
Zhu, Yanfang
Tang, Xiaojun
Xiong, Lin
Li, Jiang
Qiu, Liang
Mao, Yuan
Zhu, Jin
author_facet Gu, Xuefeng
Fu, Maoying
Ge, Zhijun
Zhan, Feng
Ding, Yuqin
Ni, Huihui
Zhang, Wei
Zhu, Yanfang
Tang, Xiaojun
Xiong, Lin
Li, Jiang
Qiu, Liang
Mao, Yuan
Zhu, Jin
author_sort Gu, Xuefeng
collection PubMed
description Melanoma-associated antigens (MAGE)-A9 has been reported to play important roles in the development of human cancers. However, the association between MAGE-A9 expression and the clinicopathological characteristics of hepatocellular carcinoma (HCC) is not well understood. The study was to detect the expression of MAGE-A9 in human HCC and investigate the association between its expression and the clinicopathological characteristics of HCC. Reverse transcription-polymerase chain reaction (RT-PCR), one-step quantitative -PCR (qPCR) and immunohistochemistry (IHC) analyses were performed to characterize the expression of MAGE-A9 in HCC cell lines and tissues. Kaplan-Meier survival and Cox regression analyses were employed to evaluate the prognosis of 100 HCC patients. The results showed that the expression of MAGE-A9 in HCC was significantly higher than that in non-cancerous cells and tissues. Moreover, the expression level of the MAGE-A9 protein in HCC was related to the pathological grade (p = 0.003), portal vein invasion (p = 0.001), distant metastasis (p = 0.022) and TNM stage (p = 0.005). Cox regression analysis further revealed that MAGE-A9 expression is an independent prognostic factor for disease-free survival (p = 0.006) and overall survival (p = 0.022). These data are the first to indicate that MAGE-A9 expression is a valuable prognostic biomarker for HCC and that high MAGE-A9 expression suggests unfavorable survival outcomes in HCC patients.
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spelling pubmed-41974152014-10-21 High expression of MAGE-A9 correlates with unfavorable survival in hepatocellular carcinoma Gu, Xuefeng Fu, Maoying Ge, Zhijun Zhan, Feng Ding, Yuqin Ni, Huihui Zhang, Wei Zhu, Yanfang Tang, Xiaojun Xiong, Lin Li, Jiang Qiu, Liang Mao, Yuan Zhu, Jin Sci Rep Article Melanoma-associated antigens (MAGE)-A9 has been reported to play important roles in the development of human cancers. However, the association between MAGE-A9 expression and the clinicopathological characteristics of hepatocellular carcinoma (HCC) is not well understood. The study was to detect the expression of MAGE-A9 in human HCC and investigate the association between its expression and the clinicopathological characteristics of HCC. Reverse transcription-polymerase chain reaction (RT-PCR), one-step quantitative -PCR (qPCR) and immunohistochemistry (IHC) analyses were performed to characterize the expression of MAGE-A9 in HCC cell lines and tissues. Kaplan-Meier survival and Cox regression analyses were employed to evaluate the prognosis of 100 HCC patients. The results showed that the expression of MAGE-A9 in HCC was significantly higher than that in non-cancerous cells and tissues. Moreover, the expression level of the MAGE-A9 protein in HCC was related to the pathological grade (p = 0.003), portal vein invasion (p = 0.001), distant metastasis (p = 0.022) and TNM stage (p = 0.005). Cox regression analysis further revealed that MAGE-A9 expression is an independent prognostic factor for disease-free survival (p = 0.006) and overall survival (p = 0.022). These data are the first to indicate that MAGE-A9 expression is a valuable prognostic biomarker for HCC and that high MAGE-A9 expression suggests unfavorable survival outcomes in HCC patients. Nature Publishing Group 2014-10-15 /pmc/articles/PMC4197415/ /pubmed/25315972 http://dx.doi.org/10.1038/srep06625 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Gu, Xuefeng
Fu, Maoying
Ge, Zhijun
Zhan, Feng
Ding, Yuqin
Ni, Huihui
Zhang, Wei
Zhu, Yanfang
Tang, Xiaojun
Xiong, Lin
Li, Jiang
Qiu, Liang
Mao, Yuan
Zhu, Jin
High expression of MAGE-A9 correlates with unfavorable survival in hepatocellular carcinoma
title High expression of MAGE-A9 correlates with unfavorable survival in hepatocellular carcinoma
title_full High expression of MAGE-A9 correlates with unfavorable survival in hepatocellular carcinoma
title_fullStr High expression of MAGE-A9 correlates with unfavorable survival in hepatocellular carcinoma
title_full_unstemmed High expression of MAGE-A9 correlates with unfavorable survival in hepatocellular carcinoma
title_short High expression of MAGE-A9 correlates with unfavorable survival in hepatocellular carcinoma
title_sort high expression of mage-a9 correlates with unfavorable survival in hepatocellular carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197415/
https://www.ncbi.nlm.nih.gov/pubmed/25315972
http://dx.doi.org/10.1038/srep06625
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