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Prognostic and clinicopathological significance of Beclin-1 in non-small-cell lung cancer: a meta-analysis
BACKGROUND: Autophagy plays a key role in the development of non-small-cell lung cancer (NSCLC). Beclin-1 is essential for the initiation and regulation of autophagy. Accumulated studies have investigated the prognostic role of Beclin-1 in NSCLC, but conclusions remain controversial. Therefore, we c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056151/ https://www.ncbi.nlm.nih.gov/pubmed/30050308 http://dx.doi.org/10.2147/OTT.S164987 |
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author | Zheng, Tianliang Li, Deping He, Zhanfeng Feng, Shuaibing Zhao, Song |
author_facet | Zheng, Tianliang Li, Deping He, Zhanfeng Feng, Shuaibing Zhao, Song |
author_sort | Zheng, Tianliang |
collection | PubMed |
description | BACKGROUND: Autophagy plays a key role in the development of non-small-cell lung cancer (NSCLC). Beclin-1 is essential for the initiation and regulation of autophagy. Accumulated studies have investigated the prognostic role of Beclin-1 in NSCLC, but conclusions remain controversial. Therefore, we conducted this meta-analysis to assess the potential significance of Beclin-1 in NSCLC. MATERIALS AND METHODS: PubMed and Embase databases were searched for eligible studies published before December 31, 2017. Odds ratio (OR) was pooled to evaluate the clinicopathological significance of Beclin-1 in NSCLC. Hazard ratio (HR) was adopted to assess the association of Beclin-1 with overall survival (OS). RESULTS: Eight studies involving 1,159 patients were included in this meta-analysis. The pooled results showed that high Beclin-1 expression was significantly correlated with earlier tumor grade (OR=0.54, 95% CI: 0.36–0.81, P=0.003), less nodal involvement (OR=0.56, 95% CI: 0.37–0.86, P=0.007), earlier TNM stage (OR=0.62, 95% CI: 0.43–0.89, P=0.010), smaller tumor size (OR=0.54, 95% CI: 0.36–0.81, P=0.003), better differentiation (OR=0.48, 95% CI: 0.36–0.64, P<0.001), and less recurrence (OR=0.24, 95% CI: 0.14–0.41, P<0.001). Moreover, high level of Beclin-1 was significantly associated with better OS in NSCLC (HR=0.41, 95% CI: 0.26–0.64, P<0.001). CONCLUSION: Our meta-analysis suggests that high Beclin-1 expression predicts a better clinicopathological status and a better prognosis in NSCLC. Beclin-1 might act as a promising prognostic biomarker for NSCLC. |
format | Online Article Text |
id | pubmed-6056151 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60561512018-07-26 Prognostic and clinicopathological significance of Beclin-1 in non-small-cell lung cancer: a meta-analysis Zheng, Tianliang Li, Deping He, Zhanfeng Feng, Shuaibing Zhao, Song Onco Targets Ther Original Research BACKGROUND: Autophagy plays a key role in the development of non-small-cell lung cancer (NSCLC). Beclin-1 is essential for the initiation and regulation of autophagy. Accumulated studies have investigated the prognostic role of Beclin-1 in NSCLC, but conclusions remain controversial. Therefore, we conducted this meta-analysis to assess the potential significance of Beclin-1 in NSCLC. MATERIALS AND METHODS: PubMed and Embase databases were searched for eligible studies published before December 31, 2017. Odds ratio (OR) was pooled to evaluate the clinicopathological significance of Beclin-1 in NSCLC. Hazard ratio (HR) was adopted to assess the association of Beclin-1 with overall survival (OS). RESULTS: Eight studies involving 1,159 patients were included in this meta-analysis. The pooled results showed that high Beclin-1 expression was significantly correlated with earlier tumor grade (OR=0.54, 95% CI: 0.36–0.81, P=0.003), less nodal involvement (OR=0.56, 95% CI: 0.37–0.86, P=0.007), earlier TNM stage (OR=0.62, 95% CI: 0.43–0.89, P=0.010), smaller tumor size (OR=0.54, 95% CI: 0.36–0.81, P=0.003), better differentiation (OR=0.48, 95% CI: 0.36–0.64, P<0.001), and less recurrence (OR=0.24, 95% CI: 0.14–0.41, P<0.001). Moreover, high level of Beclin-1 was significantly associated with better OS in NSCLC (HR=0.41, 95% CI: 0.26–0.64, P<0.001). CONCLUSION: Our meta-analysis suggests that high Beclin-1 expression predicts a better clinicopathological status and a better prognosis in NSCLC. Beclin-1 might act as a promising prognostic biomarker for NSCLC. Dove Medical Press 2018-07-19 /pmc/articles/PMC6056151/ /pubmed/30050308 http://dx.doi.org/10.2147/OTT.S164987 Text en © 2018 Zheng et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Zheng, Tianliang Li, Deping He, Zhanfeng Feng, Shuaibing Zhao, Song Prognostic and clinicopathological significance of Beclin-1 in non-small-cell lung cancer: a meta-analysis |
title | Prognostic and clinicopathological significance of Beclin-1 in non-small-cell lung cancer: a meta-analysis |
title_full | Prognostic and clinicopathological significance of Beclin-1 in non-small-cell lung cancer: a meta-analysis |
title_fullStr | Prognostic and clinicopathological significance of Beclin-1 in non-small-cell lung cancer: a meta-analysis |
title_full_unstemmed | Prognostic and clinicopathological significance of Beclin-1 in non-small-cell lung cancer: a meta-analysis |
title_short | Prognostic and clinicopathological significance of Beclin-1 in non-small-cell lung cancer: a meta-analysis |
title_sort | prognostic and clinicopathological significance of beclin-1 in non-small-cell lung cancer: a meta-analysis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056151/ https://www.ncbi.nlm.nih.gov/pubmed/30050308 http://dx.doi.org/10.2147/OTT.S164987 |
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