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Prognostic role of chromodomain helicase DNA binding protein 1-like protein in human solid cancers: A meta-analysis

BACKGROUND: Chromodomain helicase DNA binding protein 1-like (CHD1L) played vital roles in tumorigenesis and development. Its aberrant expression was reported to be related to progression and prognosis in various tumors. However, no consensus on the prognostic value of CHD1L protein has been made. T...

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Autores principales: Liu, Wanwei, Xu, Jiwei, Zhang, Caiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086487/
https://www.ncbi.nlm.nih.gov/pubmed/30024537
http://dx.doi.org/10.1097/MD.0000000000011522
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author Liu, Wanwei
Xu, Jiwei
Zhang, Caiyun
author_facet Liu, Wanwei
Xu, Jiwei
Zhang, Caiyun
author_sort Liu, Wanwei
collection PubMed
description BACKGROUND: Chromodomain helicase DNA binding protein 1-like (CHD1L) played vital roles in tumorigenesis and development. Its aberrant expression was reported to be related to progression and prognosis in various tumors. However, no consensus on the prognostic value of CHD1L protein has been made. This meta-analysis was aimed to assess the clinical significance of CHD1L protein in human solid tumors. METHODS: Web of Science, PubMed, Embase, China National Knowledge Infrastructure (CNKI), and Wanfang databases were extensively searched to retrieve publications that reported the association between CHD1L expression and cancer prognosis. Hazard ratios (HRs) or odds ratios (ORs) with their 95% confidence intervals (95% CIs) were applied to assess the strength of the associations through Stata statistical software version 12.0 or Revman software 5.3, respectively. RESULT: A total of 14 studies were screened according to the inclusion criteria. The pooled results revealed patients with higher CHD1L expression manifested with decreased overall survival (OS) (HR: 1.59, 95% CI: 1.29–1.89, P < .001) and poorer disease-free survival (DFS) (HR: 1.66, 95% CI: 1.17–2.15, P < .001). The prognostic value of CHD1L protein for OS was further confirmed by performing subgroup meta-analysis. Furthermore, the pooled results revealed a positive correlation of CHD1L protein expression with tumor depth (OR: 1.87, 95% CI: 1.48–2.37), lymph node metastasis (OR: 1.46, 95% CI: 1.01–2.11), and distant metastasis (OR: 1.86, 95% CI: 1.45–2.38). CONCLUSION: CHD1L overexpression was associated with poor prognosis and advanced clinicopathological features, CHD1L may be a valuable biomarker for prognostication of cancer patients.
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spelling pubmed-60864872018-08-17 Prognostic role of chromodomain helicase DNA binding protein 1-like protein in human solid cancers: A meta-analysis Liu, Wanwei Xu, Jiwei Zhang, Caiyun Medicine (Baltimore) Research Article BACKGROUND: Chromodomain helicase DNA binding protein 1-like (CHD1L) played vital roles in tumorigenesis and development. Its aberrant expression was reported to be related to progression and prognosis in various tumors. However, no consensus on the prognostic value of CHD1L protein has been made. This meta-analysis was aimed to assess the clinical significance of CHD1L protein in human solid tumors. METHODS: Web of Science, PubMed, Embase, China National Knowledge Infrastructure (CNKI), and Wanfang databases were extensively searched to retrieve publications that reported the association between CHD1L expression and cancer prognosis. Hazard ratios (HRs) or odds ratios (ORs) with their 95% confidence intervals (95% CIs) were applied to assess the strength of the associations through Stata statistical software version 12.0 or Revman software 5.3, respectively. RESULT: A total of 14 studies were screened according to the inclusion criteria. The pooled results revealed patients with higher CHD1L expression manifested with decreased overall survival (OS) (HR: 1.59, 95% CI: 1.29–1.89, P < .001) and poorer disease-free survival (DFS) (HR: 1.66, 95% CI: 1.17–2.15, P < .001). The prognostic value of CHD1L protein for OS was further confirmed by performing subgroup meta-analysis. Furthermore, the pooled results revealed a positive correlation of CHD1L protein expression with tumor depth (OR: 1.87, 95% CI: 1.48–2.37), lymph node metastasis (OR: 1.46, 95% CI: 1.01–2.11), and distant metastasis (OR: 1.86, 95% CI: 1.45–2.38). CONCLUSION: CHD1L overexpression was associated with poor prognosis and advanced clinicopathological features, CHD1L may be a valuable biomarker for prognostication of cancer patients. Wolters Kluwer Health 2018-07-20 /pmc/articles/PMC6086487/ /pubmed/30024537 http://dx.doi.org/10.1097/MD.0000000000011522 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Liu, Wanwei
Xu, Jiwei
Zhang, Caiyun
Prognostic role of chromodomain helicase DNA binding protein 1-like protein in human solid cancers: A meta-analysis
title Prognostic role of chromodomain helicase DNA binding protein 1-like protein in human solid cancers: A meta-analysis
title_full Prognostic role of chromodomain helicase DNA binding protein 1-like protein in human solid cancers: A meta-analysis
title_fullStr Prognostic role of chromodomain helicase DNA binding protein 1-like protein in human solid cancers: A meta-analysis
title_full_unstemmed Prognostic role of chromodomain helicase DNA binding protein 1-like protein in human solid cancers: A meta-analysis
title_short Prognostic role of chromodomain helicase DNA binding protein 1-like protein in human solid cancers: A meta-analysis
title_sort prognostic role of chromodomain helicase dna binding protein 1-like protein in human solid cancers: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086487/
https://www.ncbi.nlm.nih.gov/pubmed/30024537
http://dx.doi.org/10.1097/MD.0000000000011522
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