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Polo‐like kinase 4 correlates with greater tumor size, lymph node metastasis and confers poor survival in non‐small cell lung cancer

BACKGROUND: Our study aimed to investigate the association of polo‐like kinase 4 (PLK4) expression with tumor features as well as survival in non‐small cell lung cancer (NSCLC) patients. METHODS: Five hundred and sixty NSCLC patients who underwent pulmonary resection were recruited, and their tumor...

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Autores principales: Zhou, Qin, Fan, Gongchun, Dong, Yuanyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171315/
https://www.ncbi.nlm.nih.gov/pubmed/31876063
http://dx.doi.org/10.1002/jcla.23152
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author Zhou, Qin
Fan, Gongchun
Dong, Yuanyuan
author_facet Zhou, Qin
Fan, Gongchun
Dong, Yuanyuan
author_sort Zhou, Qin
collection PubMed
description BACKGROUND: Our study aimed to investigate the association of polo‐like kinase 4 (PLK4) expression with tumor features as well as survival in non‐small cell lung cancer (NSCLC) patients. METHODS: Five hundred and sixty NSCLC patients who underwent pulmonary resection were recruited, and their tumor specimens were obtained. Immunohistochemistry (IHC) staining was performed to assess PLK4 expression in tumor specimen. Follow‐up documents were reviewed, and the disease‐free survival (DFS) and overall survival (OS) were evaluated. RESULTS: According to IHC staining, there were 277 (49.5%) patients with PLK4 low expression and 283 (50.5%) patients with PLK4 high expression. PLK4 high expression was further classified into three different classes: high+, high++, high+++, and 122 (21.8%), 127 (22.7%), 34 (6.1%) patients were with PLK4 high+, high++, high+++ expression, respectively. Polo‐like kinase 4 expression was correlated with larger tumor size, LYN metastasis, and higher TNM stage. As for survival, DFS and OS were lower in patients with PLK4 high expression compared with patients with PLK4 low expression. In addition, DFS and OS were the lowest in patients with PLK4 high+++ expression, followed by those with PLK4 high++ expression, PLK4 high+ expression, and then patients with PLK4 low expression. Univariate and multivariate Cox's proportional hazard regression model analyses further disclosed that PLK4 was an independent predictive factor for poor DFS and OS in NSCLC patients. CONCLUSION: Our study preliminarily illuminates the clinical implication of PLK4 in NSCLC, while further studies are still needed to explicit the value of PLK4 in surveillance and treatment of NSCLC.
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spelling pubmed-71713152020-04-21 Polo‐like kinase 4 correlates with greater tumor size, lymph node metastasis and confers poor survival in non‐small cell lung cancer Zhou, Qin Fan, Gongchun Dong, Yuanyuan J Clin Lab Anal Research Articles BACKGROUND: Our study aimed to investigate the association of polo‐like kinase 4 (PLK4) expression with tumor features as well as survival in non‐small cell lung cancer (NSCLC) patients. METHODS: Five hundred and sixty NSCLC patients who underwent pulmonary resection were recruited, and their tumor specimens were obtained. Immunohistochemistry (IHC) staining was performed to assess PLK4 expression in tumor specimen. Follow‐up documents were reviewed, and the disease‐free survival (DFS) and overall survival (OS) were evaluated. RESULTS: According to IHC staining, there were 277 (49.5%) patients with PLK4 low expression and 283 (50.5%) patients with PLK4 high expression. PLK4 high expression was further classified into three different classes: high+, high++, high+++, and 122 (21.8%), 127 (22.7%), 34 (6.1%) patients were with PLK4 high+, high++, high+++ expression, respectively. Polo‐like kinase 4 expression was correlated with larger tumor size, LYN metastasis, and higher TNM stage. As for survival, DFS and OS were lower in patients with PLK4 high expression compared with patients with PLK4 low expression. In addition, DFS and OS were the lowest in patients with PLK4 high+++ expression, followed by those with PLK4 high++ expression, PLK4 high+ expression, and then patients with PLK4 low expression. Univariate and multivariate Cox's proportional hazard regression model analyses further disclosed that PLK4 was an independent predictive factor for poor DFS and OS in NSCLC patients. CONCLUSION: Our study preliminarily illuminates the clinical implication of PLK4 in NSCLC, while further studies are still needed to explicit the value of PLK4 in surveillance and treatment of NSCLC. John Wiley and Sons Inc. 2019-12-25 /pmc/articles/PMC7171315/ /pubmed/31876063 http://dx.doi.org/10.1002/jcla.23152 Text en © 2019 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, 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 Research Articles
Zhou, Qin
Fan, Gongchun
Dong, Yuanyuan
Polo‐like kinase 4 correlates with greater tumor size, lymph node metastasis and confers poor survival in non‐small cell lung cancer
title Polo‐like kinase 4 correlates with greater tumor size, lymph node metastasis and confers poor survival in non‐small cell lung cancer
title_full Polo‐like kinase 4 correlates with greater tumor size, lymph node metastasis and confers poor survival in non‐small cell lung cancer
title_fullStr Polo‐like kinase 4 correlates with greater tumor size, lymph node metastasis and confers poor survival in non‐small cell lung cancer
title_full_unstemmed Polo‐like kinase 4 correlates with greater tumor size, lymph node metastasis and confers poor survival in non‐small cell lung cancer
title_short Polo‐like kinase 4 correlates with greater tumor size, lymph node metastasis and confers poor survival in non‐small cell lung cancer
title_sort polo‐like kinase 4 correlates with greater tumor size, lymph node metastasis and confers poor survival in non‐small cell lung cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171315/
https://www.ncbi.nlm.nih.gov/pubmed/31876063
http://dx.doi.org/10.1002/jcla.23152
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