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Prognostic roles of mitochondrial transcription termination factors in non-small cell lung cancer

Mitochondrial transcription termination factors (MTERFs) regulate mitochondrial gene transcription and metabolism in numerous types of cells. Previous studies have indicated that MTERFs serve pivotal roles in the pathogenesis of various cancer types. However, the expression and prognostic roles of M...

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Autores principales: Sun, Shuangyan, Wu, Chunjiao, Yang, Changliang, Chen, Jian, Wang, Xiu, Nan, Yingji, Huang, Zhicheng, Ma, Lixia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732965/
https://www.ncbi.nlm.nih.gov/pubmed/31516563
http://dx.doi.org/10.3892/ol.2019.10680
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author Sun, Shuangyan
Wu, Chunjiao
Yang, Changliang
Chen, Jian
Wang, Xiu
Nan, Yingji
Huang, Zhicheng
Ma, Lixia
author_facet Sun, Shuangyan
Wu, Chunjiao
Yang, Changliang
Chen, Jian
Wang, Xiu
Nan, Yingji
Huang, Zhicheng
Ma, Lixia
author_sort Sun, Shuangyan
collection PubMed
description Mitochondrial transcription termination factors (MTERFs) regulate mitochondrial gene transcription and metabolism in numerous types of cells. Previous studies have indicated that MTERFs serve pivotal roles in the pathogenesis of various cancer types. However, the expression and prognostic roles of MTERFs in patients with non-small cell lung cancer (NSCLC) remain elusive. The present study investigated the gene alteration frequency and expression level using Gene Expression Omnibus datasets and reverse transcription-quantitative polymerase chain reaction, and evaluated the prognostic roles of MTERFs in patients with NSCLC using the Kaplan-Meier plotter database. In human lung cancer tissues, it was observed that the mRNA levels of MTERF1, 2, 3 and 4 were positively associated with the copy number of these genes. The mRNA expression levels of MTERF1 and 3 were significantly increased in NSCLC tissues compared with adjacent non-tumor tissues; however, the mRNA expression of MTERF2 was significantly decreased in NSCLC tissues. High mRNA expression levels of MTERF1, 2, 3 and 4 were strongly associated with an improved overall survival rate (OS) in patients with lung adenocarcinoma. Additionally, high mRNA expression levels of MTERF1, 2, 3 and 4 were also strongly associated with an improved OS of patients with NSCLC in the earlier stages of disease (stage I) or patients with negative surgical margins. These results indicate the critical prognostic values of MTERF expression levels in NSCLC. The findings of the present study may be beneficial for understanding the molecular biology mechanism of NSCLC and for generating effective therapeutic approaches for patients with NSCLC.
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spelling pubmed-67329652019-09-12 Prognostic roles of mitochondrial transcription termination factors in non-small cell lung cancer Sun, Shuangyan Wu, Chunjiao Yang, Changliang Chen, Jian Wang, Xiu Nan, Yingji Huang, Zhicheng Ma, Lixia Oncol Lett Articles Mitochondrial transcription termination factors (MTERFs) regulate mitochondrial gene transcription and metabolism in numerous types of cells. Previous studies have indicated that MTERFs serve pivotal roles in the pathogenesis of various cancer types. However, the expression and prognostic roles of MTERFs in patients with non-small cell lung cancer (NSCLC) remain elusive. The present study investigated the gene alteration frequency and expression level using Gene Expression Omnibus datasets and reverse transcription-quantitative polymerase chain reaction, and evaluated the prognostic roles of MTERFs in patients with NSCLC using the Kaplan-Meier plotter database. In human lung cancer tissues, it was observed that the mRNA levels of MTERF1, 2, 3 and 4 were positively associated with the copy number of these genes. The mRNA expression levels of MTERF1 and 3 were significantly increased in NSCLC tissues compared with adjacent non-tumor tissues; however, the mRNA expression of MTERF2 was significantly decreased in NSCLC tissues. High mRNA expression levels of MTERF1, 2, 3 and 4 were strongly associated with an improved overall survival rate (OS) in patients with lung adenocarcinoma. Additionally, high mRNA expression levels of MTERF1, 2, 3 and 4 were also strongly associated with an improved OS of patients with NSCLC in the earlier stages of disease (stage I) or patients with negative surgical margins. These results indicate the critical prognostic values of MTERF expression levels in NSCLC. The findings of the present study may be beneficial for understanding the molecular biology mechanism of NSCLC and for generating effective therapeutic approaches for patients with NSCLC. D.A. Spandidos 2019-10 2019-07-29 /pmc/articles/PMC6732965/ /pubmed/31516563 http://dx.doi.org/10.3892/ol.2019.10680 Text en Copyright: © Sun 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
Sun, Shuangyan
Wu, Chunjiao
Yang, Changliang
Chen, Jian
Wang, Xiu
Nan, Yingji
Huang, Zhicheng
Ma, Lixia
Prognostic roles of mitochondrial transcription termination factors in non-small cell lung cancer
title Prognostic roles of mitochondrial transcription termination factors in non-small cell lung cancer
title_full Prognostic roles of mitochondrial transcription termination factors in non-small cell lung cancer
title_fullStr Prognostic roles of mitochondrial transcription termination factors in non-small cell lung cancer
title_full_unstemmed Prognostic roles of mitochondrial transcription termination factors in non-small cell lung cancer
title_short Prognostic roles of mitochondrial transcription termination factors in non-small cell lung cancer
title_sort prognostic roles of mitochondrial transcription termination factors in non-small cell lung cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732965/
https://www.ncbi.nlm.nih.gov/pubmed/31516563
http://dx.doi.org/10.3892/ol.2019.10680
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