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Prognostic role of microRNAs in human gastrointestinal cancer: A systematic review and meta-analysis

BACKGROUND: Gastrointestinal cancers (GICs) mainly including esophageal, gastric and colorectal cancer, are the most common cause of cancer-related death and lead into high mortality worldwide. We performed this systematic review and meta-analysis to elucidate relationship between multiple microRNAs...

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Autores principales: Zheng, Qiang, Chen, Changyu, Guan, Haiyang, Kang, Weibiao, Yu, Changjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542297/
https://www.ncbi.nlm.nih.gov/pubmed/28402940
http://dx.doi.org/10.18632/oncotarget.16679
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author Zheng, Qiang
Chen, Changyu
Guan, Haiyang
Kang, Weibiao
Yu, Changjun
author_facet Zheng, Qiang
Chen, Changyu
Guan, Haiyang
Kang, Weibiao
Yu, Changjun
author_sort Zheng, Qiang
collection PubMed
description BACKGROUND: Gastrointestinal cancers (GICs) mainly including esophageal, gastric and colorectal cancer, are the most common cause of cancer-related death and lead into high mortality worldwide. We performed this systematic review and meta-analysis to elucidate relationship between multiple microRNAs (miRs) expression and survival of GIC patients. METHODS: We searched a wide range of database. Fixed-effects and random-effects models were used to calculate the pooled hazard ratio values of overall survival and disease free survival. In addition, funnel plots were used to qualitatively analyze the publication bias and verified by Begg's test while it seems asymmetry. RESULTS: 60 studies involving a total of 6225 patients (1271 with esophageal cancer, 3467 with gastric cancer and 1517 with colorectal cancer) were included in our meta-analysis. The pooled hazard ratio values of overall survival related to different miRs expression in esophageal, gastric, colorectal and gastrointestinal cancer were 2.10 (1.78-2.49), 2.02 (1.83-2.23), 2.54 (2.14-3.02) and 2.15 (1.99-2.31), respectively. We have identified a total of 59 miRs including 23 significantly up-regulated expression miRs (miR-214, miR-17, miR-20a, miR-200c, miR-107, miR-27a, etc.) and 36 significantly down-regulated expression miRs (miR-433, let-7g, miR-125a-5p, miR-760, miR-206, miR-26a, miR-200b, miR-185, etc.) correlated with poor prognosis in GIC patients. Moreover, 35 of them revealed mechanisms. CONCLUSION: Overall, specific miRs are significantly associated with the prognosis of GIC patients and potentially eligible for the prediction of patients survival. It also provides a potential value for clinical decision-making development and may serve as a promising miR-based target therapy waiting for further elucidation.
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spelling pubmed-55422972017-08-07 Prognostic role of microRNAs in human gastrointestinal cancer: A systematic review and meta-analysis Zheng, Qiang Chen, Changyu Guan, Haiyang Kang, Weibiao Yu, Changjun Oncotarget Review BACKGROUND: Gastrointestinal cancers (GICs) mainly including esophageal, gastric and colorectal cancer, are the most common cause of cancer-related death and lead into high mortality worldwide. We performed this systematic review and meta-analysis to elucidate relationship between multiple microRNAs (miRs) expression and survival of GIC patients. METHODS: We searched a wide range of database. Fixed-effects and random-effects models were used to calculate the pooled hazard ratio values of overall survival and disease free survival. In addition, funnel plots were used to qualitatively analyze the publication bias and verified by Begg's test while it seems asymmetry. RESULTS: 60 studies involving a total of 6225 patients (1271 with esophageal cancer, 3467 with gastric cancer and 1517 with colorectal cancer) were included in our meta-analysis. The pooled hazard ratio values of overall survival related to different miRs expression in esophageal, gastric, colorectal and gastrointestinal cancer were 2.10 (1.78-2.49), 2.02 (1.83-2.23), 2.54 (2.14-3.02) and 2.15 (1.99-2.31), respectively. We have identified a total of 59 miRs including 23 significantly up-regulated expression miRs (miR-214, miR-17, miR-20a, miR-200c, miR-107, miR-27a, etc.) and 36 significantly down-regulated expression miRs (miR-433, let-7g, miR-125a-5p, miR-760, miR-206, miR-26a, miR-200b, miR-185, etc.) correlated with poor prognosis in GIC patients. Moreover, 35 of them revealed mechanisms. CONCLUSION: Overall, specific miRs are significantly associated with the prognosis of GIC patients and potentially eligible for the prediction of patients survival. It also provides a potential value for clinical decision-making development and may serve as a promising miR-based target therapy waiting for further elucidation. Impact Journals LLC 2017-03-29 /pmc/articles/PMC5542297/ /pubmed/28402940 http://dx.doi.org/10.18632/oncotarget.16679 Text en Copyright: © 2017 Zheng et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Review
Zheng, Qiang
Chen, Changyu
Guan, Haiyang
Kang, Weibiao
Yu, Changjun
Prognostic role of microRNAs in human gastrointestinal cancer: A systematic review and meta-analysis
title Prognostic role of microRNAs in human gastrointestinal cancer: A systematic review and meta-analysis
title_full Prognostic role of microRNAs in human gastrointestinal cancer: A systematic review and meta-analysis
title_fullStr Prognostic role of microRNAs in human gastrointestinal cancer: A systematic review and meta-analysis
title_full_unstemmed Prognostic role of microRNAs in human gastrointestinal cancer: A systematic review and meta-analysis
title_short Prognostic role of microRNAs in human gastrointestinal cancer: A systematic review and meta-analysis
title_sort prognostic role of micrornas in human gastrointestinal cancer: a systematic review and meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542297/
https://www.ncbi.nlm.nih.gov/pubmed/28402940
http://dx.doi.org/10.18632/oncotarget.16679
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