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Prognostic and clinicopathological significance of MLKL expression in cancer patients: a meta-analysis

BACKGROUND: MLKL is the most important executor of necroptosis pathway. Recent studies have demonstrated that MLKL could serve as a potential prognostic biomarker for cancer patients. However, most studies reported so far are limited in discrete outcome and sample size. METHODS: We systematically se...

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Autores principales: Hu, Binwu, Shi, Deyao, Lv, Xiao, Chen, Songfeng, Huang, Qin, Xie, Mao, Shao, Zengwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044038/
https://www.ncbi.nlm.nih.gov/pubmed/30005626
http://dx.doi.org/10.1186/s12885-018-4655-4
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author Hu, Binwu
Shi, Deyao
Lv, Xiao
Chen, Songfeng
Huang, Qin
Xie, Mao
Shao, Zengwu
author_facet Hu, Binwu
Shi, Deyao
Lv, Xiao
Chen, Songfeng
Huang, Qin
Xie, Mao
Shao, Zengwu
author_sort Hu, Binwu
collection PubMed
description BACKGROUND: MLKL is the most important executor of necroptosis pathway. Recent studies have demonstrated that MLKL could serve as a potential prognostic biomarker for cancer patients. However, most studies reported so far are limited in discrete outcome and sample size. METHODS: We systematically searched PubMed, Embase, Web of Science and CNKI to obtain all relevant articles about the prognostic value of abnormally expressed MLKL in patients with any type of tumor. Odds ratios or hazards ratios (HRs) with corresponding 95% confidence intervals (CIs) were pooled to estimate the association between MLKL expression and clinicopathological characteristics or survival of cancer patients. RESULTS: A total of 6 eligible studies with 613 cancer patients were enrolled in our meta-analysis. Our results demonstrated that decreased expression level of MLKL was significantly associated with poor overall survival (OS) (pooled HR 0.26, 95%CI 0.17–0.40, high/low) and event-free survival (EFS) (pooled HR 0.45, 95%CI 0.23–0.87, high/low) in cancer patients. Furthermore, subgroup analysis divided by type of cancer, sample size, follow-up time and Newcastle–Ottawa Scale (NOS) score showed consistent prognostic value. In addition, our analysis revealed that decreased expression level of MLKL was significantly associated with advanced tumor stage, more lymph node metastasis and older age. CONCLUSIONS: In conclusion, our meta-analysis suggested that decreased MLKL expression might be a convinced unfavorable prognostic factor that could help the clinical decision-making process.
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spelling pubmed-60440382018-07-13 Prognostic and clinicopathological significance of MLKL expression in cancer patients: a meta-analysis Hu, Binwu Shi, Deyao Lv, Xiao Chen, Songfeng Huang, Qin Xie, Mao Shao, Zengwu BMC Cancer Research Article BACKGROUND: MLKL is the most important executor of necroptosis pathway. Recent studies have demonstrated that MLKL could serve as a potential prognostic biomarker for cancer patients. However, most studies reported so far are limited in discrete outcome and sample size. METHODS: We systematically searched PubMed, Embase, Web of Science and CNKI to obtain all relevant articles about the prognostic value of abnormally expressed MLKL in patients with any type of tumor. Odds ratios or hazards ratios (HRs) with corresponding 95% confidence intervals (CIs) were pooled to estimate the association between MLKL expression and clinicopathological characteristics or survival of cancer patients. RESULTS: A total of 6 eligible studies with 613 cancer patients were enrolled in our meta-analysis. Our results demonstrated that decreased expression level of MLKL was significantly associated with poor overall survival (OS) (pooled HR 0.26, 95%CI 0.17–0.40, high/low) and event-free survival (EFS) (pooled HR 0.45, 95%CI 0.23–0.87, high/low) in cancer patients. Furthermore, subgroup analysis divided by type of cancer, sample size, follow-up time and Newcastle–Ottawa Scale (NOS) score showed consistent prognostic value. In addition, our analysis revealed that decreased expression level of MLKL was significantly associated with advanced tumor stage, more lymph node metastasis and older age. CONCLUSIONS: In conclusion, our meta-analysis suggested that decreased MLKL expression might be a convinced unfavorable prognostic factor that could help the clinical decision-making process. BioMed Central 2018-07-13 /pmc/articles/PMC6044038/ /pubmed/30005626 http://dx.doi.org/10.1186/s12885-018-4655-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hu, Binwu
Shi, Deyao
Lv, Xiao
Chen, Songfeng
Huang, Qin
Xie, Mao
Shao, Zengwu
Prognostic and clinicopathological significance of MLKL expression in cancer patients: a meta-analysis
title Prognostic and clinicopathological significance of MLKL expression in cancer patients: a meta-analysis
title_full Prognostic and clinicopathological significance of MLKL expression in cancer patients: a meta-analysis
title_fullStr Prognostic and clinicopathological significance of MLKL expression in cancer patients: a meta-analysis
title_full_unstemmed Prognostic and clinicopathological significance of MLKL expression in cancer patients: a meta-analysis
title_short Prognostic and clinicopathological significance of MLKL expression in cancer patients: a meta-analysis
title_sort prognostic and clinicopathological significance of mlkl expression in cancer patients: a meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044038/
https://www.ncbi.nlm.nih.gov/pubmed/30005626
http://dx.doi.org/10.1186/s12885-018-4655-4
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