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Clinicopathological and Prognostic Role of Long Noncoding RNA Linc00152 in Various Human Neoplasms: Evidence from Meta-Analysis

Recent researches have demonstrated that long noncoding RNA linc00152 was aberrantly upregulated in multiple tumor types. High expression of linc00152 was associated with poor outcomes in cancer patients. Therefore, we conducted this meta-analysis to evaluate its potential value as a prognostic pred...

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Autores principales: Miao, Chenkui, Zhao, Kai, Zhu, Jundong, Liang, Chao, Xu, Aiming, Hua, Yibo, Zhang, Jianzhong, Liu, Shouyong, Tian, Ye, Zhang, Chao, Wang, Yuhao, Su, Shifeng, Wang, Zengjun, Liu, Bianjiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733223/
https://www.ncbi.nlm.nih.gov/pubmed/29285514
http://dx.doi.org/10.1155/2017/6010721
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author Miao, Chenkui
Zhao, Kai
Zhu, Jundong
Liang, Chao
Xu, Aiming
Hua, Yibo
Zhang, Jianzhong
Liu, Shouyong
Tian, Ye
Zhang, Chao
Wang, Yuhao
Su, Shifeng
Wang, Zengjun
Liu, Bianjiang
author_facet Miao, Chenkui
Zhao, Kai
Zhu, Jundong
Liang, Chao
Xu, Aiming
Hua, Yibo
Zhang, Jianzhong
Liu, Shouyong
Tian, Ye
Zhang, Chao
Wang, Yuhao
Su, Shifeng
Wang, Zengjun
Liu, Bianjiang
author_sort Miao, Chenkui
collection PubMed
description Recent researches have demonstrated that long noncoding RNA linc00152 was aberrantly upregulated in multiple tumor types. High expression of linc00152 was associated with poor outcomes in cancer patients. Therefore, we conducted this meta-analysis to evaluate its potential value as a prognostic predictor in various human neoplasms. Eligible studies were searched through several electronic databases including PubMed, Embase, Web of Science, and the Cochrane Library. Eight original studies including 752 cancer patients were ultimately enrolled. Statistical analysis suggested that overexpression of linc00152 was significantly correlated with unfavorable overall survival (OS) (HR = 2.05, 95% CI: 1.59–2.64) and disease-free/progression-free survival (DFS/PFS) (HR = 3.52, 95% CI: 1.82–6.79) in cancer patients. In addition, a significant correlation was observed between aberrant linc000152 expression and lymph node metastasis (LNM) (OR = 2.49, 95% CI: 1.57–3.94) but not in vessel invasion (VI) (OR = 1.02, 95% CI: 0.54–1.93) and distant metastasis (DM) (OR = 0.600, 95% CI: 0.213–1.689). Our meta-analysis demonstrated that high linc00152 expression significantly predicted inferior OS and DFS/PFS in multiple neoplasms, as well as advanced LNM and VI. Linc00152 may serve as a potential indicator in predicting poor outcomes and metastases of diverse cancers.
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spelling pubmed-57332232017-12-28 Clinicopathological and Prognostic Role of Long Noncoding RNA Linc00152 in Various Human Neoplasms: Evidence from Meta-Analysis Miao, Chenkui Zhao, Kai Zhu, Jundong Liang, Chao Xu, Aiming Hua, Yibo Zhang, Jianzhong Liu, Shouyong Tian, Ye Zhang, Chao Wang, Yuhao Su, Shifeng Wang, Zengjun Liu, Bianjiang Biomed Res Int Review Article Recent researches have demonstrated that long noncoding RNA linc00152 was aberrantly upregulated in multiple tumor types. High expression of linc00152 was associated with poor outcomes in cancer patients. Therefore, we conducted this meta-analysis to evaluate its potential value as a prognostic predictor in various human neoplasms. Eligible studies were searched through several electronic databases including PubMed, Embase, Web of Science, and the Cochrane Library. Eight original studies including 752 cancer patients were ultimately enrolled. Statistical analysis suggested that overexpression of linc00152 was significantly correlated with unfavorable overall survival (OS) (HR = 2.05, 95% CI: 1.59–2.64) and disease-free/progression-free survival (DFS/PFS) (HR = 3.52, 95% CI: 1.82–6.79) in cancer patients. In addition, a significant correlation was observed between aberrant linc000152 expression and lymph node metastasis (LNM) (OR = 2.49, 95% CI: 1.57–3.94) but not in vessel invasion (VI) (OR = 1.02, 95% CI: 0.54–1.93) and distant metastasis (DM) (OR = 0.600, 95% CI: 0.213–1.689). Our meta-analysis demonstrated that high linc00152 expression significantly predicted inferior OS and DFS/PFS in multiple neoplasms, as well as advanced LNM and VI. Linc00152 may serve as a potential indicator in predicting poor outcomes and metastases of diverse cancers. Hindawi 2017 2017-11-23 /pmc/articles/PMC5733223/ /pubmed/29285514 http://dx.doi.org/10.1155/2017/6010721 Text en Copyright © 2017 Chenkui Miao et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Miao, Chenkui
Zhao, Kai
Zhu, Jundong
Liang, Chao
Xu, Aiming
Hua, Yibo
Zhang, Jianzhong
Liu, Shouyong
Tian, Ye
Zhang, Chao
Wang, Yuhao
Su, Shifeng
Wang, Zengjun
Liu, Bianjiang
Clinicopathological and Prognostic Role of Long Noncoding RNA Linc00152 in Various Human Neoplasms: Evidence from Meta-Analysis
title Clinicopathological and Prognostic Role of Long Noncoding RNA Linc00152 in Various Human Neoplasms: Evidence from Meta-Analysis
title_full Clinicopathological and Prognostic Role of Long Noncoding RNA Linc00152 in Various Human Neoplasms: Evidence from Meta-Analysis
title_fullStr Clinicopathological and Prognostic Role of Long Noncoding RNA Linc00152 in Various Human Neoplasms: Evidence from Meta-Analysis
title_full_unstemmed Clinicopathological and Prognostic Role of Long Noncoding RNA Linc00152 in Various Human Neoplasms: Evidence from Meta-Analysis
title_short Clinicopathological and Prognostic Role of Long Noncoding RNA Linc00152 in Various Human Neoplasms: Evidence from Meta-Analysis
title_sort clinicopathological and prognostic role of long noncoding rna linc00152 in various human neoplasms: evidence from meta-analysis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5733223/
https://www.ncbi.nlm.nih.gov/pubmed/29285514
http://dx.doi.org/10.1155/2017/6010721
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