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High expression of monocarboxylate transporter 4 predicts poor prognosis in patients with lung adenocarcinoma

Monocarboxylate transporter 4 (MCT-4) serves a key function in transporting lactate across the plasma membrane in various types of human cancer. Evidence indicates that MCT-4 expression is associated with non-small cell lung cancer; however, the distribution and clinical significance of MCT-4 in the...

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Autores principales: Ruan, Yushu, Zeng, Fanjun, Cheng, Zhiqiang, Zhao, Xianda, Fu, Pin, Chen, Honglei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661367/
https://www.ncbi.nlm.nih.gov/pubmed/29113201
http://dx.doi.org/10.3892/ol.2017.6964
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author Ruan, Yushu
Zeng, Fanjun
Cheng, Zhiqiang
Zhao, Xianda
Fu, Pin
Chen, Honglei
author_facet Ruan, Yushu
Zeng, Fanjun
Cheng, Zhiqiang
Zhao, Xianda
Fu, Pin
Chen, Honglei
author_sort Ruan, Yushu
collection PubMed
description Monocarboxylate transporter 4 (MCT-4) serves a key function in transporting lactate across the plasma membrane in various types of human cancer. Evidence indicates that MCT-4 expression is associated with non-small cell lung cancer; however, the distribution and clinical significance of MCT-4 in the lung adenocarcinoma (AC) subtype remain unknown. Thus, the aim of the present study was to explore the clinicopathological significance and prognostic values of MCT-4 expression in lung AC. Quantum dots-based immunofluorescence histochemistry was performed to observe the expression of MCT-4 in 146 specimens of lung AC and corresponding normal lung tissues. MCT-4 protein and mRNA were detected by western blotting and reverse transcription-quantitative polymerase chain reaction from 30 fresh samples of lung AC and corresponding normal lung tissues. Of the 146 samples, 25 (17.1%) exhibited high and 121 (82.9%) exhibited low MCT-4 expression. MCT-4, at the protein and mRNA level, was significantly increased in tumor specimens compared with corresponding normal lung tissue (P<0.05). MCT-4 protein expression was significantly associated with depth of invasion (P=0.034). A survival curve analysis indicated that high MCT-4 expression in lung AC was associated with a decreased overall survival rate (P=0.001). Multivariate analysis demonstrated that high MCT-4 level was an independent prognostic factor (hazard ratio, 3.192; 95% confidence interval, 1.804–5.646; P=0.001) for patients with lung AC. The results have demonstrated that high MCT-4 expression is significantly associated with the poor prognosis and disease progression of patients with lung AC. Therefore, MCT-4 may be a candidate therapeutic target in lung AC.
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spelling pubmed-56613672017-11-06 High expression of monocarboxylate transporter 4 predicts poor prognosis in patients with lung adenocarcinoma Ruan, Yushu Zeng, Fanjun Cheng, Zhiqiang Zhao, Xianda Fu, Pin Chen, Honglei Oncol Lett Articles Monocarboxylate transporter 4 (MCT-4) serves a key function in transporting lactate across the plasma membrane in various types of human cancer. Evidence indicates that MCT-4 expression is associated with non-small cell lung cancer; however, the distribution and clinical significance of MCT-4 in the lung adenocarcinoma (AC) subtype remain unknown. Thus, the aim of the present study was to explore the clinicopathological significance and prognostic values of MCT-4 expression in lung AC. Quantum dots-based immunofluorescence histochemistry was performed to observe the expression of MCT-4 in 146 specimens of lung AC and corresponding normal lung tissues. MCT-4 protein and mRNA were detected by western blotting and reverse transcription-quantitative polymerase chain reaction from 30 fresh samples of lung AC and corresponding normal lung tissues. Of the 146 samples, 25 (17.1%) exhibited high and 121 (82.9%) exhibited low MCT-4 expression. MCT-4, at the protein and mRNA level, was significantly increased in tumor specimens compared with corresponding normal lung tissue (P<0.05). MCT-4 protein expression was significantly associated with depth of invasion (P=0.034). A survival curve analysis indicated that high MCT-4 expression in lung AC was associated with a decreased overall survival rate (P=0.001). Multivariate analysis demonstrated that high MCT-4 level was an independent prognostic factor (hazard ratio, 3.192; 95% confidence interval, 1.804–5.646; P=0.001) for patients with lung AC. The results have demonstrated that high MCT-4 expression is significantly associated with the poor prognosis and disease progression of patients with lung AC. Therefore, MCT-4 may be a candidate therapeutic target in lung AC. D.A. Spandidos 2017-11 2017-09-15 /pmc/articles/PMC5661367/ /pubmed/29113201 http://dx.doi.org/10.3892/ol.2017.6964 Text en Copyright: © Ruan et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Ruan, Yushu
Zeng, Fanjun
Cheng, Zhiqiang
Zhao, Xianda
Fu, Pin
Chen, Honglei
High expression of monocarboxylate transporter 4 predicts poor prognosis in patients with lung adenocarcinoma
title High expression of monocarboxylate transporter 4 predicts poor prognosis in patients with lung adenocarcinoma
title_full High expression of monocarboxylate transporter 4 predicts poor prognosis in patients with lung adenocarcinoma
title_fullStr High expression of monocarboxylate transporter 4 predicts poor prognosis in patients with lung adenocarcinoma
title_full_unstemmed High expression of monocarboxylate transporter 4 predicts poor prognosis in patients with lung adenocarcinoma
title_short High expression of monocarboxylate transporter 4 predicts poor prognosis in patients with lung adenocarcinoma
title_sort high expression of monocarboxylate transporter 4 predicts poor prognosis in patients with lung adenocarcinoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5661367/
https://www.ncbi.nlm.nih.gov/pubmed/29113201
http://dx.doi.org/10.3892/ol.2017.6964
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