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Prognostic and clinicopathological significance of nm23-H1 expression in non-small cell lung cancer: A meta-analysis

The relationship between the expression of nm23-H1 and the invasion and prognosis of non-small cell lung cancer (NSCLC) is still controversial. Therefore, we conducted a meta-analysis to determine the prognostic value of nm23-H1 in patients with NSCLC. And to explore the relationship between the exp...

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Autores principales: Li, Dailong, Li, Wanqiang, Tian, Cheng, Pang, Yaqi, Xu, Lu, Wang, Yuke, Xu, Xinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524916/
https://www.ncbi.nlm.nih.gov/pubmed/36181032
http://dx.doi.org/10.1097/MD.0000000000030815
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author Li, Dailong
Li, Wanqiang
Tian, Cheng
Pang, Yaqi
Xu, Lu
Wang, Yuke
Xu, Xinhua
author_facet Li, Dailong
Li, Wanqiang
Tian, Cheng
Pang, Yaqi
Xu, Lu
Wang, Yuke
Xu, Xinhua
author_sort Li, Dailong
collection PubMed
description The relationship between the expression of nm23-H1 and the invasion and prognosis of non-small cell lung cancer (NSCLC) is still controversial. Therefore, we conducted a meta-analysis to determine the prognostic value of nm23-H1 in patients with NSCLC. And to explore the relationship between the expression of nm23-H1 and clinicopathological features in patients with NSCLC. METHODS: Literature search in PubMed, EMBASE, Cochrane Library, CNKI, and WanFang database was performed up to June 14, 2021. Studies on the expression and clinical significance of nm23-H1 in NSCLC were included. According to the inclusion and exclusion criteria, 2 researchers independently screened the literatures, extracted the data, and evaluated the quality. Meta-analysis was performed using RevMan 5.4 software (Nordic Cochran Centre, Copenhagen, Denmark). RESULTS: Twenty-five studies met our inclusion criteria and were finally included for the analysis, involving 2198 participants. Our meta-analysis revealed that nm23-H1 expression was associated with tumor differentiation (OR = 0.54, 95% CI: 0.42–0.70, P < .00001), TNM stage (OR = 1.70, 95% CI: 1.23–2.34, P = .001), and lymph node status (OR = 0.26, 95% CI, 0.17–0.39, P < .00001), but have no associate with sex, age, pathological type, and T stages. Additionally, low nm23-H1 expression reduced the 3-year survival rate (OR = 2.74, 95% CI: 1.54–4.86, P = .0006) and 5-year survival rate (OR = 2.78, 95% CI: 1.36–5.69, P = .005). CONCLUSION: Nm23-H1 can be used as a biomarker to predict tumor invasiveness and evaluate the prognosis of patients with NSCLC.
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spelling pubmed-95249162022-10-03 Prognostic and clinicopathological significance of nm23-H1 expression in non-small cell lung cancer: A meta-analysis Li, Dailong Li, Wanqiang Tian, Cheng Pang, Yaqi Xu, Lu Wang, Yuke Xu, Xinhua Medicine (Baltimore) Research Article The relationship between the expression of nm23-H1 and the invasion and prognosis of non-small cell lung cancer (NSCLC) is still controversial. Therefore, we conducted a meta-analysis to determine the prognostic value of nm23-H1 in patients with NSCLC. And to explore the relationship between the expression of nm23-H1 and clinicopathological features in patients with NSCLC. METHODS: Literature search in PubMed, EMBASE, Cochrane Library, CNKI, and WanFang database was performed up to June 14, 2021. Studies on the expression and clinical significance of nm23-H1 in NSCLC were included. According to the inclusion and exclusion criteria, 2 researchers independently screened the literatures, extracted the data, and evaluated the quality. Meta-analysis was performed using RevMan 5.4 software (Nordic Cochran Centre, Copenhagen, Denmark). RESULTS: Twenty-five studies met our inclusion criteria and were finally included for the analysis, involving 2198 participants. Our meta-analysis revealed that nm23-H1 expression was associated with tumor differentiation (OR = 0.54, 95% CI: 0.42–0.70, P < .00001), TNM stage (OR = 1.70, 95% CI: 1.23–2.34, P = .001), and lymph node status (OR = 0.26, 95% CI, 0.17–0.39, P < .00001), but have no associate with sex, age, pathological type, and T stages. Additionally, low nm23-H1 expression reduced the 3-year survival rate (OR = 2.74, 95% CI: 1.54–4.86, P = .0006) and 5-year survival rate (OR = 2.78, 95% CI: 1.36–5.69, P = .005). CONCLUSION: Nm23-H1 can be used as a biomarker to predict tumor invasiveness and evaluate the prognosis of patients with NSCLC. Lippincott Williams & Wilkins 2022-09-30 /pmc/articles/PMC9524916/ /pubmed/36181032 http://dx.doi.org/10.1097/MD.0000000000030815 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle Research Article
Li, Dailong
Li, Wanqiang
Tian, Cheng
Pang, Yaqi
Xu, Lu
Wang, Yuke
Xu, Xinhua
Prognostic and clinicopathological significance of nm23-H1 expression in non-small cell lung cancer: A meta-analysis
title Prognostic and clinicopathological significance of nm23-H1 expression in non-small cell lung cancer: A meta-analysis
title_full Prognostic and clinicopathological significance of nm23-H1 expression in non-small cell lung cancer: A meta-analysis
title_fullStr Prognostic and clinicopathological significance of nm23-H1 expression in non-small cell lung cancer: A meta-analysis
title_full_unstemmed Prognostic and clinicopathological significance of nm23-H1 expression in non-small cell lung cancer: A meta-analysis
title_short Prognostic and clinicopathological significance of nm23-H1 expression in non-small cell lung cancer: A meta-analysis
title_sort prognostic and clinicopathological significance of nm23-h1 expression in non-small cell lung cancer: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9524916/
https://www.ncbi.nlm.nih.gov/pubmed/36181032
http://dx.doi.org/10.1097/MD.0000000000030815
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