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Long noncoding RNA AFAP1-AS1, a potential novel biomarker to predict the clinical outcome of cancer patients: a meta-analysis

A number of studies have demonstrated that the expression level of actin filament-associated protein 1 antisense RNA 1 (AFAP1-AS1) was upregulated in various cancers. High expression of AFAP1-AS1 is associated with an increased risk of metastasis and a poor prognosis in cancer patients. The electron...

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Autores principales: Liu, Fang-teng, Xue, Qi-zhen, Zhu, Pei-qian, Luo, Hong-liang, Zhang, Yi, Hao, Tengfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948684/
https://www.ncbi.nlm.nih.gov/pubmed/27471399
http://dx.doi.org/10.2147/OTT.S107188
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author Liu, Fang-teng
Xue, Qi-zhen
Zhu, Pei-qian
Luo, Hong-liang
Zhang, Yi
Hao, Tengfei
author_facet Liu, Fang-teng
Xue, Qi-zhen
Zhu, Pei-qian
Luo, Hong-liang
Zhang, Yi
Hao, Tengfei
author_sort Liu, Fang-teng
collection PubMed
description A number of studies have demonstrated that the expression level of actin filament-associated protein 1 antisense RNA 1 (AFAP1-AS1) was upregulated in various cancers. High expression of AFAP1-AS1 is associated with an increased risk of metastasis and a poor prognosis in cancer patients. The electronic search was conducted in PubMed, EMBASE, Cochrane Library, China National Knowledge Infrastructure, and Wanfang database. We collected relevant articles to explore the association between the expression levels of AFAP1-AS1 and lymph node metastasis, distant metastasis, overall survival, relapse-free survival, and progression-free survival. A total of 1,017 patients from eight studies were finally included. The results showed that cancer patients with high AFAP1-AS1 expression suffered an increased risk of developing lymph node metastasis (odds ratio =3.19, 95% confidence interval [CI]: 2.11–4.83, P<0.00001) and distant metastasis (odds ratio =3.05, 95% CI: 1.84–5.04, P<0.0001). Moreover, we found that patients with high AFAP1-AS1 expression also had a poorer overall survival (hazard ratio [HR]: 1.98, 95% CI: 1.57–2.38, P=0.000), a worse progression-free survival (HR: 1.73, 95% CI: 1.11–2.35, P=0.000), and a shorter recurrence-free survival (HR: 1.96, 95% CI: 1.02–2.90, P=0.000) than those with low AFAP1-AS1 expression. High expression of AFAP1-AS1 was associated with poor clinical outcome. AFAP1-AS1 might serve as a potential novel biomarker for indicating the clinical outcomes in human cancers.
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spelling pubmed-49486842016-07-28 Long noncoding RNA AFAP1-AS1, a potential novel biomarker to predict the clinical outcome of cancer patients: a meta-analysis Liu, Fang-teng Xue, Qi-zhen Zhu, Pei-qian Luo, Hong-liang Zhang, Yi Hao, Tengfei Onco Targets Ther Original Research A number of studies have demonstrated that the expression level of actin filament-associated protein 1 antisense RNA 1 (AFAP1-AS1) was upregulated in various cancers. High expression of AFAP1-AS1 is associated with an increased risk of metastasis and a poor prognosis in cancer patients. The electronic search was conducted in PubMed, EMBASE, Cochrane Library, China National Knowledge Infrastructure, and Wanfang database. We collected relevant articles to explore the association between the expression levels of AFAP1-AS1 and lymph node metastasis, distant metastasis, overall survival, relapse-free survival, and progression-free survival. A total of 1,017 patients from eight studies were finally included. The results showed that cancer patients with high AFAP1-AS1 expression suffered an increased risk of developing lymph node metastasis (odds ratio =3.19, 95% confidence interval [CI]: 2.11–4.83, P<0.00001) and distant metastasis (odds ratio =3.05, 95% CI: 1.84–5.04, P<0.0001). Moreover, we found that patients with high AFAP1-AS1 expression also had a poorer overall survival (hazard ratio [HR]: 1.98, 95% CI: 1.57–2.38, P=0.000), a worse progression-free survival (HR: 1.73, 95% CI: 1.11–2.35, P=0.000), and a shorter recurrence-free survival (HR: 1.96, 95% CI: 1.02–2.90, P=0.000) than those with low AFAP1-AS1 expression. High expression of AFAP1-AS1 was associated with poor clinical outcome. AFAP1-AS1 might serve as a potential novel biomarker for indicating the clinical outcomes in human cancers. Dove Medical Press 2016-07-12 /pmc/articles/PMC4948684/ /pubmed/27471399 http://dx.doi.org/10.2147/OTT.S107188 Text en © 2016 Liu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Liu, Fang-teng
Xue, Qi-zhen
Zhu, Pei-qian
Luo, Hong-liang
Zhang, Yi
Hao, Tengfei
Long noncoding RNA AFAP1-AS1, a potential novel biomarker to predict the clinical outcome of cancer patients: a meta-analysis
title Long noncoding RNA AFAP1-AS1, a potential novel biomarker to predict the clinical outcome of cancer patients: a meta-analysis
title_full Long noncoding RNA AFAP1-AS1, a potential novel biomarker to predict the clinical outcome of cancer patients: a meta-analysis
title_fullStr Long noncoding RNA AFAP1-AS1, a potential novel biomarker to predict the clinical outcome of cancer patients: a meta-analysis
title_full_unstemmed Long noncoding RNA AFAP1-AS1, a potential novel biomarker to predict the clinical outcome of cancer patients: a meta-analysis
title_short Long noncoding RNA AFAP1-AS1, a potential novel biomarker to predict the clinical outcome of cancer patients: a meta-analysis
title_sort long noncoding rna afap1-as1, a potential novel biomarker to predict the clinical outcome of cancer patients: a meta-analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948684/
https://www.ncbi.nlm.nih.gov/pubmed/27471399
http://dx.doi.org/10.2147/OTT.S107188
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