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The role of Livin expression in the clinicopathological features and prognosis of lung cancer: a meta-analysis

BACKGROUND: While the impact of Livin expression on patients with lung cancer was evaluated in previous studies, the results remained debatable. The relationship between Livin expression and clinicopathological features and prognosis in lung cancer was assessed in the present meta-analysis. METHODS:...

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Autores principales: Fei, Min, Luo, Yingquan, Zhou, Jian, Yan, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798057/
https://www.ncbi.nlm.nih.gov/pubmed/35116243
http://dx.doi.org/10.21037/tcr-20-2835
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author Fei, Min
Luo, Yingquan
Zhou, Jian
Yan, Qian
author_facet Fei, Min
Luo, Yingquan
Zhou, Jian
Yan, Qian
author_sort Fei, Min
collection PubMed
description BACKGROUND: While the impact of Livin expression on patients with lung cancer was evaluated in previous studies, the results remained debatable. The relationship between Livin expression and clinicopathological features and prognosis in lung cancer was assessed in the present meta-analysis. METHODS: Web of Science, PubMed, Embase, Springer, Cochrane Library, China National Knowledge Internet database (CNKI), Wanfang database, Chinese VIP database and Chinese Biological Medical Database (CBM) were searched for relevant publications analyzing the role of Livin in prognosis and clinicopathological features of lung cancer before September 2020. The results were evaluated using pooled odds ratio (OR) and 95% confidence intervals (CIs) calculated by STATA 12.0 software. RESULTS: Twenty studies with a total of 1,395 patients were enrolled in this meta-analysis based on inclusion and exclusion criteria. Livin expression was significantly associated with smoking status (OR =2.51, 95% CI: 1.70–3.72, P<0.05), lung adenocarcinomas (LAC) (OR =2.16, 95% CI: 1.60–2.92, P<0.05), TNM stage (OR =2.49, 95% CI: 1.63–3.69, P<0.05) and poor differentiation (OR =2.04, 95% CI: 1.35–3.08, P<0.05). Livin expression was significantly related to metastasis (OR =4.22, 95% CI: 2.68–6.64, P<0.05) and lower 5-year overall survival (OR =4.23, 95% CI: 2.60–6.88, P<0.05) of patients with lung cancer. CONCLUSIONS: The results of our study manifested that Livin expression was significantly related to smoking status, LAC, high TNM stage, poor differentiation, metastasis and 5-year overall survival rate, which indicated that Livin may be a potential biomarker for prognosis of lung cancer.
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spelling pubmed-87980572022-02-02 The role of Livin expression in the clinicopathological features and prognosis of lung cancer: a meta-analysis Fei, Min Luo, Yingquan Zhou, Jian Yan, Qian Transl Cancer Res Original Article BACKGROUND: While the impact of Livin expression on patients with lung cancer was evaluated in previous studies, the results remained debatable. The relationship between Livin expression and clinicopathological features and prognosis in lung cancer was assessed in the present meta-analysis. METHODS: Web of Science, PubMed, Embase, Springer, Cochrane Library, China National Knowledge Internet database (CNKI), Wanfang database, Chinese VIP database and Chinese Biological Medical Database (CBM) were searched for relevant publications analyzing the role of Livin in prognosis and clinicopathological features of lung cancer before September 2020. The results were evaluated using pooled odds ratio (OR) and 95% confidence intervals (CIs) calculated by STATA 12.0 software. RESULTS: Twenty studies with a total of 1,395 patients were enrolled in this meta-analysis based on inclusion and exclusion criteria. Livin expression was significantly associated with smoking status (OR =2.51, 95% CI: 1.70–3.72, P<0.05), lung adenocarcinomas (LAC) (OR =2.16, 95% CI: 1.60–2.92, P<0.05), TNM stage (OR =2.49, 95% CI: 1.63–3.69, P<0.05) and poor differentiation (OR =2.04, 95% CI: 1.35–3.08, P<0.05). Livin expression was significantly related to metastasis (OR =4.22, 95% CI: 2.68–6.64, P<0.05) and lower 5-year overall survival (OR =4.23, 95% CI: 2.60–6.88, P<0.05) of patients with lung cancer. CONCLUSIONS: The results of our study manifested that Livin expression was significantly related to smoking status, LAC, high TNM stage, poor differentiation, metastasis and 5-year overall survival rate, which indicated that Livin may be a potential biomarker for prognosis of lung cancer. AME Publishing Company 2021-01 /pmc/articles/PMC8798057/ /pubmed/35116243 http://dx.doi.org/10.21037/tcr-20-2835 Text en 2021 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Fei, Min
Luo, Yingquan
Zhou, Jian
Yan, Qian
The role of Livin expression in the clinicopathological features and prognosis of lung cancer: a meta-analysis
title The role of Livin expression in the clinicopathological features and prognosis of lung cancer: a meta-analysis
title_full The role of Livin expression in the clinicopathological features and prognosis of lung cancer: a meta-analysis
title_fullStr The role of Livin expression in the clinicopathological features and prognosis of lung cancer: a meta-analysis
title_full_unstemmed The role of Livin expression in the clinicopathological features and prognosis of lung cancer: a meta-analysis
title_short The role of Livin expression in the clinicopathological features and prognosis of lung cancer: a meta-analysis
title_sort role of livin expression in the clinicopathological features and prognosis of lung cancer: a meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798057/
https://www.ncbi.nlm.nih.gov/pubmed/35116243
http://dx.doi.org/10.21037/tcr-20-2835
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