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Published in: Tumor Biology 1/2014

01-01-2014 | Research Article

Overexpression of MACC1 protein and its clinical implications in patients with glioma

Authors: Tao Yang, Bin Kong, Yong-Qin Kuang, Lin Cheng, Jian-Wen Gu, Jun-Hai Zhang, Hai-Feng Shu, Si-Xun Yu, Wei-Qi He, Xue-Min Xing, Hai-Dong Huang

Published in: Tumor Biology | Issue 1/2014

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Abstract

Metastasis associated in colon cancer 1 (MACC1) has been regarded as a novel potential therapeutic target for multiple cancers. However, the impact of MACC1 in glioma remains unclear. The aim of this study was to analyze the correlation of MACC1 expression with the clinicopathological features of glioma. MACC1 mRNA and protein expression levels in human glioma tissues were detected by quantitative real-time polymerase chain reaction and immunohistochemistry assays, respectively. MACC1 mRNA and protein expression were both significantly higher in glioma tissues than in corresponding noncancerous brain tissues (both P < 0.001). In addition, statistical analysis suggested that high MACC1 expression was significantly correlated with advanced pathological grade (P = 0.004) and that patients with high expression of MACC1 protein exhibited a poorer prognosis than those with low MACC1 expression. Furthermore, Cox multivariate analysis showed that MACC1 overexpression was an independent prognostic factor for predicting the overall survival of glioma patients. In conclusion, expression of MACC1 in glioma could be adopted as a candidate biomarker for the diagnosis of clinical stage and for assessing prognosis, indicating for the first time that MACC1 may play an important role in the tumor development and progression in glioma. MACC1 might be considered as a novel therapeutic target against this cancer.
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Metadata
Title
Overexpression of MACC1 protein and its clinical implications in patients with glioma
Authors
Tao Yang
Bin Kong
Yong-Qin Kuang
Lin Cheng
Jian-Wen Gu
Jun-Hai Zhang
Hai-Feng Shu
Si-Xun Yu
Wei-Qi He
Xue-Min Xing
Hai-Dong Huang
Publication date
01-01-2014
Publisher
Springer Netherlands
Published in
Tumor Biology / Issue 1/2014
Print ISSN: 1010-4283
Electronic ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-013-1112-5

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