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Circulating microRNAs in plasma of patients with gastric cancers
BACKGROUND: We examined plasma microRNA (miRNA) concentrations from patients with gastric cancers (GCs) to assess their clinical application for diagnosing and monitoring diseases. METHODS: We initially investigated the appropriateness of plasma miRNA assay, and then compared plasma miRNA results wi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853097/ https://www.ncbi.nlm.nih.gov/pubmed/20234369 http://dx.doi.org/10.1038/sj.bjc.6605608 |
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author | Tsujiura, M Ichikawa, D Komatsu, S Shiozaki, A Takeshita, H Kosuga, T Konishi, H Morimura, R Deguchi, K Fujiwara, H Okamoto, K Otsuji, E |
author_facet | Tsujiura, M Ichikawa, D Komatsu, S Shiozaki, A Takeshita, H Kosuga, T Konishi, H Morimura, R Deguchi, K Fujiwara, H Okamoto, K Otsuji, E |
author_sort | Tsujiura, M |
collection | PubMed |
description | BACKGROUND: We examined plasma microRNA (miRNA) concentrations from patients with gastric cancers (GCs) to assess their clinical application for diagnosing and monitoring diseases. METHODS: We initially investigated the appropriateness of plasma miRNA assay, and then compared plasma miRNA results with the expressions in cancer tissues from eight GC patients, and also compared plasma miRNAs between pre- and post-operative paired samples from 10 GC patients. Then, plasma miRNAs (miR-17-5p, miR-21, miR-106a, miR-106b and let-7a) were analysed in 69 GC patients and 30 healthy volunteers in total. RESULTS: The initial analysis showed that miRNAs were stable and detectable in all plasma samples, and the plasma miRNA levels reflected the tumour miRNAs in most cases. The levels of these miRNAs were significantly reduced in post-operative samples. In large-scale analysis, the plasma concentrations of miRNAs (miR-17-5p, miR-21, miR-106a, miR-106b) were significantly higher in GC patients than controls (P=0.05, 0.006, 0.008 and <0.001 respectively), whereas let-7a was lower in GC patients (P=0.002). The values of the area under the receiver-operating characteristic curve were 0.721 for the miR-106b assay and 0.879 for the miR-106a/let-7a ratio assay. CONCLUSION: Detection of circulating miRNAs might provide new complementary tumour markers for GC. |
format | Text |
id | pubmed-2853097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-28530972011-03-30 Circulating microRNAs in plasma of patients with gastric cancers Tsujiura, M Ichikawa, D Komatsu, S Shiozaki, A Takeshita, H Kosuga, T Konishi, H Morimura, R Deguchi, K Fujiwara, H Okamoto, K Otsuji, E Br J Cancer Molecular Diagnostics BACKGROUND: We examined plasma microRNA (miRNA) concentrations from patients with gastric cancers (GCs) to assess their clinical application for diagnosing and monitoring diseases. METHODS: We initially investigated the appropriateness of plasma miRNA assay, and then compared plasma miRNA results with the expressions in cancer tissues from eight GC patients, and also compared plasma miRNAs between pre- and post-operative paired samples from 10 GC patients. Then, plasma miRNAs (miR-17-5p, miR-21, miR-106a, miR-106b and let-7a) were analysed in 69 GC patients and 30 healthy volunteers in total. RESULTS: The initial analysis showed that miRNAs were stable and detectable in all plasma samples, and the plasma miRNA levels reflected the tumour miRNAs in most cases. The levels of these miRNAs were significantly reduced in post-operative samples. In large-scale analysis, the plasma concentrations of miRNAs (miR-17-5p, miR-21, miR-106a, miR-106b) were significantly higher in GC patients than controls (P=0.05, 0.006, 0.008 and <0.001 respectively), whereas let-7a was lower in GC patients (P=0.002). The values of the area under the receiver-operating characteristic curve were 0.721 for the miR-106b assay and 0.879 for the miR-106a/let-7a ratio assay. CONCLUSION: Detection of circulating miRNAs might provide new complementary tumour markers for GC. Nature Publishing Group 2010-03-30 2010-03-16 /pmc/articles/PMC2853097/ /pubmed/20234369 http://dx.doi.org/10.1038/sj.bjc.6605608 Text en Copyright © 2010 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Tsujiura, M Ichikawa, D Komatsu, S Shiozaki, A Takeshita, H Kosuga, T Konishi, H Morimura, R Deguchi, K Fujiwara, H Okamoto, K Otsuji, E Circulating microRNAs in plasma of patients with gastric cancers |
title | Circulating microRNAs in plasma of patients with gastric cancers |
title_full | Circulating microRNAs in plasma of patients with gastric cancers |
title_fullStr | Circulating microRNAs in plasma of patients with gastric cancers |
title_full_unstemmed | Circulating microRNAs in plasma of patients with gastric cancers |
title_short | Circulating microRNAs in plasma of patients with gastric cancers |
title_sort | circulating micrornas in plasma of patients with gastric cancers |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853097/ https://www.ncbi.nlm.nih.gov/pubmed/20234369 http://dx.doi.org/10.1038/sj.bjc.6605608 |
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