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Serum microRNA expression profile: miR-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma

BACKGROUND: Recent studies have demonstrated that microRNAs (miRNAs) are stably detectable in blood and can serve as useful biomarkers for cancer. METHODS: We performed an miRNA array using serum samples obtained from oesophageal squamous cell carcinoma (ESCC) patients or healthy controls. MiR-1246...

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Autores principales: Takeshita, N, Hoshino, I, Mori, M, Akutsu, Y, Hanari, N, Yoneyama, Y, Ikeda, N, Isozaki, Y, Maruyama, T, Akanuma, N, Komatsu, A, Jitsukawa, M, Matsubara, H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593570/
https://www.ncbi.nlm.nih.gov/pubmed/23361059
http://dx.doi.org/10.1038/bjc.2013.8
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author Takeshita, N
Hoshino, I
Mori, M
Akutsu, Y
Hanari, N
Yoneyama, Y
Ikeda, N
Isozaki, Y
Maruyama, T
Akanuma, N
Komatsu, A
Jitsukawa, M
Matsubara, H
author_facet Takeshita, N
Hoshino, I
Mori, M
Akutsu, Y
Hanari, N
Yoneyama, Y
Ikeda, N
Isozaki, Y
Maruyama, T
Akanuma, N
Komatsu, A
Jitsukawa, M
Matsubara, H
author_sort Takeshita, N
collection PubMed
description BACKGROUND: Recent studies have demonstrated that microRNAs (miRNAs) are stably detectable in blood and can serve as useful biomarkers for cancer. METHODS: We performed an miRNA array using serum samples obtained from oesophageal squamous cell carcinoma (ESCC) patients or healthy controls. MiR-1246 was the most markedly elevated in ESCC patients. Therefore, miR-1246 was selected as a candidate for further analysis. The serum miR-1246 level in 46 healthy controls and 101 ESCC patients was evaluated and compared among various clinicopathological characteristics. MiR-1246 expressions in tissue, exosomal, and cellular samples were also examined. RESULTS: Serum miR-1246 alone yielded an receiver-operating characteristic curve area of 0.754, with 71.3% sensitivity and 73.9% specificity for distinguishing ESCC patients from healthy controls. Serum miR-1246 was significantly correlated with the TNM stage and showed to be the strongest independent risk factor for poor survival (HR, 4.032; P=0.017). Unlike the tendency shown in previous reports, miR-1246 was not upregulated in ESCC tissue samples. Furthermore, exosomal miR-1246 did not reflect the abundance in the cell of origin. CONCLUSION: These data support our contention that serum miR-1246 has strong potential as a novel diagnostic and prognostic biomarker in ESCC, and its releasing mechanism is selective and independent of tissue miRNA abundance.
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spelling pubmed-35935702014-02-19 Serum microRNA expression profile: miR-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma Takeshita, N Hoshino, I Mori, M Akutsu, Y Hanari, N Yoneyama, Y Ikeda, N Isozaki, Y Maruyama, T Akanuma, N Komatsu, A Jitsukawa, M Matsubara, H Br J Cancer Molecular Diagnostics BACKGROUND: Recent studies have demonstrated that microRNAs (miRNAs) are stably detectable in blood and can serve as useful biomarkers for cancer. METHODS: We performed an miRNA array using serum samples obtained from oesophageal squamous cell carcinoma (ESCC) patients or healthy controls. MiR-1246 was the most markedly elevated in ESCC patients. Therefore, miR-1246 was selected as a candidate for further analysis. The serum miR-1246 level in 46 healthy controls and 101 ESCC patients was evaluated and compared among various clinicopathological characteristics. MiR-1246 expressions in tissue, exosomal, and cellular samples were also examined. RESULTS: Serum miR-1246 alone yielded an receiver-operating characteristic curve area of 0.754, with 71.3% sensitivity and 73.9% specificity for distinguishing ESCC patients from healthy controls. Serum miR-1246 was significantly correlated with the TNM stage and showed to be the strongest independent risk factor for poor survival (HR, 4.032; P=0.017). Unlike the tendency shown in previous reports, miR-1246 was not upregulated in ESCC tissue samples. Furthermore, exosomal miR-1246 did not reflect the abundance in the cell of origin. CONCLUSION: These data support our contention that serum miR-1246 has strong potential as a novel diagnostic and prognostic biomarker in ESCC, and its releasing mechanism is selective and independent of tissue miRNA abundance. Nature Publishing Group 2013-02-19 2013-01-29 /pmc/articles/PMC3593570/ /pubmed/23361059 http://dx.doi.org/10.1038/bjc.2013.8 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Molecular Diagnostics
Takeshita, N
Hoshino, I
Mori, M
Akutsu, Y
Hanari, N
Yoneyama, Y
Ikeda, N
Isozaki, Y
Maruyama, T
Akanuma, N
Komatsu, A
Jitsukawa, M
Matsubara, H
Serum microRNA expression profile: miR-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma
title Serum microRNA expression profile: miR-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma
title_full Serum microRNA expression profile: miR-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma
title_fullStr Serum microRNA expression profile: miR-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma
title_full_unstemmed Serum microRNA expression profile: miR-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma
title_short Serum microRNA expression profile: miR-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma
title_sort serum microrna expression profile: mir-1246 as a novel diagnostic and prognostic biomarker for oesophageal squamous cell carcinoma
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593570/
https://www.ncbi.nlm.nih.gov/pubmed/23361059
http://dx.doi.org/10.1038/bjc.2013.8
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