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Upregulation of circulating miR130a is correlated with development of Barrett’s esophagus and esophageal adenocarcinoma
BACKGROUND: Barrett’s esophagus (BE) is one of the major known risk factors for esophageal adenocarcinoma (EAC). Circulating miRNAs are emerging as predictive biomarkers for early detection of malignancy. However, the potential for circulating miRNAs to be used as biomarkers for BE neoplastic progre...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301302/ https://www.ncbi.nlm.nih.gov/pubmed/30588024 http://dx.doi.org/10.2147/OTT.S162603 |
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author | Wang, Li Ji, Feng Liu, Gang Wang, Wei Li, Zhitong Yue, Yongqiang Wang, Zhonggao |
author_facet | Wang, Li Ji, Feng Liu, Gang Wang, Wei Li, Zhitong Yue, Yongqiang Wang, Zhonggao |
author_sort | Wang, Li |
collection | PubMed |
description | BACKGROUND: Barrett’s esophagus (BE) is one of the major known risk factors for esophageal adenocarcinoma (EAC). Circulating miRNAs are emerging as predictive biomarkers for early detection of malignancy. However, the potential for circulating miRNAs to be used as biomarkers for BE neoplastic progression to EAC has not been well characterized. METHOD: We performed a systematic screening approach to identify spectrum miRNAs in the serum of both BE and EAC patients. RESULTS: miRNA-array web-based software identified 116 sequences differentially expressed between BE patients and healthy controls. Subsequent study revealed that miR130a was significantly upregulated in serum samples of BE and EAC patients compared to healthy controls. We found an increase in serum miR130a in low-grade and high-grade dysplasia BE patients compared to individuals with metaplasia. We also observed that miR130a expression levels increased gradually from early-stage (I, II) to advanced-stage (III, IV) EAC patients. CONCLUSION: Our preliminary results provide evidence that circulating miR130a is correlated with the development of BE and EAC. |
format | Online Article Text |
id | pubmed-6301302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63013022018-12-26 Upregulation of circulating miR130a is correlated with development of Barrett’s esophagus and esophageal adenocarcinoma Wang, Li Ji, Feng Liu, Gang Wang, Wei Li, Zhitong Yue, Yongqiang Wang, Zhonggao Onco Targets Ther Original Research BACKGROUND: Barrett’s esophagus (BE) is one of the major known risk factors for esophageal adenocarcinoma (EAC). Circulating miRNAs are emerging as predictive biomarkers for early detection of malignancy. However, the potential for circulating miRNAs to be used as biomarkers for BE neoplastic progression to EAC has not been well characterized. METHOD: We performed a systematic screening approach to identify spectrum miRNAs in the serum of both BE and EAC patients. RESULTS: miRNA-array web-based software identified 116 sequences differentially expressed between BE patients and healthy controls. Subsequent study revealed that miR130a was significantly upregulated in serum samples of BE and EAC patients compared to healthy controls. We found an increase in serum miR130a in low-grade and high-grade dysplasia BE patients compared to individuals with metaplasia. We also observed that miR130a expression levels increased gradually from early-stage (I, II) to advanced-stage (III, IV) EAC patients. CONCLUSION: Our preliminary results provide evidence that circulating miR130a is correlated with the development of BE and EAC. Dove Medical Press 2018-12-17 /pmc/articles/PMC6301302/ /pubmed/30588024 http://dx.doi.org/10.2147/OTT.S162603 Text en © 2019 Wang 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 Wang, Li Ji, Feng Liu, Gang Wang, Wei Li, Zhitong Yue, Yongqiang Wang, Zhonggao Upregulation of circulating miR130a is correlated with development of Barrett’s esophagus and esophageal adenocarcinoma |
title | Upregulation of circulating miR130a is correlated with development of Barrett’s esophagus and esophageal adenocarcinoma |
title_full | Upregulation of circulating miR130a is correlated with development of Barrett’s esophagus and esophageal adenocarcinoma |
title_fullStr | Upregulation of circulating miR130a is correlated with development of Barrett’s esophagus and esophageal adenocarcinoma |
title_full_unstemmed | Upregulation of circulating miR130a is correlated with development of Barrett’s esophagus and esophageal adenocarcinoma |
title_short | Upregulation of circulating miR130a is correlated with development of Barrett’s esophagus and esophageal adenocarcinoma |
title_sort | upregulation of circulating mir130a is correlated with development of barrett’s esophagus and esophageal adenocarcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6301302/ https://www.ncbi.nlm.nih.gov/pubmed/30588024 http://dx.doi.org/10.2147/OTT.S162603 |
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