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Salivary MicroRNAs as Promising Biomarkers for Detection of Esophageal Cancer
BACKGROUND AND PURPOSE: Tissue microRNAs (miRNAs) can detect cancers and predict prognosis. Several recent studies reported that tissue, plasma, and saliva miRNAs share similar expression profiles. In this study, we investigated the discriminatory power of salivary miRNAs (including whole saliva and...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613402/ https://www.ncbi.nlm.nih.gov/pubmed/23560033 http://dx.doi.org/10.1371/journal.pone.0057502 |
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author | Xie, Zijun Chen, Gang Zhang, Xuchao Li, Dongfeng Huang, Jian Yang, Cuiqin Zhang, Pingyong Qin, Yuxuan Duan, Yifan Gong, Bo Li, Zijun |
author_facet | Xie, Zijun Chen, Gang Zhang, Xuchao Li, Dongfeng Huang, Jian Yang, Cuiqin Zhang, Pingyong Qin, Yuxuan Duan, Yifan Gong, Bo Li, Zijun |
author_sort | Xie, Zijun |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Tissue microRNAs (miRNAs) can detect cancers and predict prognosis. Several recent studies reported that tissue, plasma, and saliva miRNAs share similar expression profiles. In this study, we investigated the discriminatory power of salivary miRNAs (including whole saliva and saliva supernatant) for detection of esophageal cancer. MATERIALS AND METHODS: By Agilent microarray, six deregulated miRNAs from whole saliva samples from seven patients with esophageal cancer and three healthy controls were selected. The six selected miRNAs were subjected to validation of their expression levels by RT-qPCR using both whole saliva and saliva supernatant samples from an independent set of 39 patients with esophageal cancer and 19 healthy controls. RESULTS: Six miRNAs (miR-10b*, miR-144, miR-21, miR-451, miR-486-5p, and miR-634) were identified as targets by Agilent microarray. After validation by RT-qPCR, miR-10b*, miR-144, and miR-451 in whole saliva and miR-10b*, miR-144, miR-21, and miR-451 in saliva supernatant were significantly upregulated in patients, with sensitivities of 89.7, 92.3, 84.6, 79.5, 43.6, 89.7, and 51.3% and specificities of 57.9, 47.4, 57.9%, 57.9, 89.5, 47.4, and 84.2%, respectively. CONCLUSIONS: We found distinctive miRNAs for esophageal cancer in both whole saliva and saliva supernatant. These miRNAs possess discriminatory power for detection of esophageal cancer. Because saliva collection is noninvasive and convenient, salivary miRNAs show great promise as biomarkers for detection of esophageal cancer in areas at high risk. |
format | Online Article Text |
id | pubmed-3613402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36134022013-04-04 Salivary MicroRNAs as Promising Biomarkers for Detection of Esophageal Cancer Xie, Zijun Chen, Gang Zhang, Xuchao Li, Dongfeng Huang, Jian Yang, Cuiqin Zhang, Pingyong Qin, Yuxuan Duan, Yifan Gong, Bo Li, Zijun PLoS One Research Article BACKGROUND AND PURPOSE: Tissue microRNAs (miRNAs) can detect cancers and predict prognosis. Several recent studies reported that tissue, plasma, and saliva miRNAs share similar expression profiles. In this study, we investigated the discriminatory power of salivary miRNAs (including whole saliva and saliva supernatant) for detection of esophageal cancer. MATERIALS AND METHODS: By Agilent microarray, six deregulated miRNAs from whole saliva samples from seven patients with esophageal cancer and three healthy controls were selected. The six selected miRNAs were subjected to validation of their expression levels by RT-qPCR using both whole saliva and saliva supernatant samples from an independent set of 39 patients with esophageal cancer and 19 healthy controls. RESULTS: Six miRNAs (miR-10b*, miR-144, miR-21, miR-451, miR-486-5p, and miR-634) were identified as targets by Agilent microarray. After validation by RT-qPCR, miR-10b*, miR-144, and miR-451 in whole saliva and miR-10b*, miR-144, miR-21, and miR-451 in saliva supernatant were significantly upregulated in patients, with sensitivities of 89.7, 92.3, 84.6, 79.5, 43.6, 89.7, and 51.3% and specificities of 57.9, 47.4, 57.9%, 57.9, 89.5, 47.4, and 84.2%, respectively. CONCLUSIONS: We found distinctive miRNAs for esophageal cancer in both whole saliva and saliva supernatant. These miRNAs possess discriminatory power for detection of esophageal cancer. Because saliva collection is noninvasive and convenient, salivary miRNAs show great promise as biomarkers for detection of esophageal cancer in areas at high risk. Public Library of Science 2013-04-01 /pmc/articles/PMC3613402/ /pubmed/23560033 http://dx.doi.org/10.1371/journal.pone.0057502 Text en © 2013 Xie et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Xie, Zijun Chen, Gang Zhang, Xuchao Li, Dongfeng Huang, Jian Yang, Cuiqin Zhang, Pingyong Qin, Yuxuan Duan, Yifan Gong, Bo Li, Zijun Salivary MicroRNAs as Promising Biomarkers for Detection of Esophageal Cancer |
title | Salivary MicroRNAs as Promising Biomarkers for Detection of Esophageal Cancer |
title_full | Salivary MicroRNAs as Promising Biomarkers for Detection of Esophageal Cancer |
title_fullStr | Salivary MicroRNAs as Promising Biomarkers for Detection of Esophageal Cancer |
title_full_unstemmed | Salivary MicroRNAs as Promising Biomarkers for Detection of Esophageal Cancer |
title_short | Salivary MicroRNAs as Promising Biomarkers for Detection of Esophageal Cancer |
title_sort | salivary micrornas as promising biomarkers for detection of esophageal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613402/ https://www.ncbi.nlm.nih.gov/pubmed/23560033 http://dx.doi.org/10.1371/journal.pone.0057502 |
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