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Real-Time PCR-Based Analysis of the Human Bile MicroRNAome Identifies miR-9 as a Potential Diagnostic Biomarker for Biliary Tract Cancer

Biliary tract cancer (BTC) is often difficult to diagnose definitively, even through histological examination. MicroRNAs (miRNAs) regulate a variety of physiological processes. In recent years, it has been suggested that profiles for circulating miRNAs, as well as those for tissue miRNAs, have the p...

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Autores principales: Shigehara, Kengo, Yokomuro, Shigeki, Ishibashi, Osamu, Mizuguchi, Yoshiaki, Arima, Yasuo, Kawahigashi, Yutaka, Kanda, Tomohiro, Akagi, Ichiro, Tajiri, Takashi, Yoshida, Hiroshi, Takizawa, Toshihiro, Uchida, Eiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157401/
https://www.ncbi.nlm.nih.gov/pubmed/21858175
http://dx.doi.org/10.1371/journal.pone.0023584
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author Shigehara, Kengo
Yokomuro, Shigeki
Ishibashi, Osamu
Mizuguchi, Yoshiaki
Arima, Yasuo
Kawahigashi, Yutaka
Kanda, Tomohiro
Akagi, Ichiro
Tajiri, Takashi
Yoshida, Hiroshi
Takizawa, Toshihiro
Uchida, Eiji
author_facet Shigehara, Kengo
Yokomuro, Shigeki
Ishibashi, Osamu
Mizuguchi, Yoshiaki
Arima, Yasuo
Kawahigashi, Yutaka
Kanda, Tomohiro
Akagi, Ichiro
Tajiri, Takashi
Yoshida, Hiroshi
Takizawa, Toshihiro
Uchida, Eiji
author_sort Shigehara, Kengo
collection PubMed
description Biliary tract cancer (BTC) is often difficult to diagnose definitively, even through histological examination. MicroRNAs (miRNAs) regulate a variety of physiological processes. In recent years, it has been suggested that profiles for circulating miRNAs, as well as those for tissue miRNAs, have the potential to be used as diagnostic biomarkers for cancer. The aim of this study was to confirm the existence of miRNAs in human bile and to assess their potential as clinical biomarkers for BTC. We sampled bile from patients who underwent biliary drainage for biliary diseases such as BTC and choledocholithiasis. PCR-based miRNA detection and miRNA cloning were performed to identify bile miRNAs. Using high-throughput real-time PCR-based miRNA microarrays, the expression profiles of 667 miRNAs were compared in patients with malignant disease (n = 9) and age-matched patients with the benign disease choledocholithiasis (n = 9). We subsequently characterized bile miRNAs in terms of stability and localization. Through cloning and using PCR methods, we confirmed that miRNAs exist in bile. Differential analysis of bile miRNAs demonstrated that 10 of the 667 miRNAs were significantly more highly expressed in the malignant group than in the benign group at P<0.0005. Setting the specificity threshold to 100% showed that some miRNAs (miR-9, miR-302c*, miR-199a-3p and miR-222*) had a sensitivity level of 88.9%, and receiver-operating characteristic analysis demonstrated that miR-9 and miR-145* could be useful diagnostic markers for BTC. Moreover, we verified the long-term stability of miRNAs in bile, a characteristic that makes them suitable for diagnostic use in clinical settings. We also confirmed that bile miRNAs are localized to the malignant/benign biliary epithelia. These findings suggest that bile miRNAs could be informative biomarkers for hepatobiliary disease and that some miRNAs, particularly miR-9, may be helpful in the diagnosis and clinical management of BTC.
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spelling pubmed-31574012011-08-19 Real-Time PCR-Based Analysis of the Human Bile MicroRNAome Identifies miR-9 as a Potential Diagnostic Biomarker for Biliary Tract Cancer Shigehara, Kengo Yokomuro, Shigeki Ishibashi, Osamu Mizuguchi, Yoshiaki Arima, Yasuo Kawahigashi, Yutaka Kanda, Tomohiro Akagi, Ichiro Tajiri, Takashi Yoshida, Hiroshi Takizawa, Toshihiro Uchida, Eiji PLoS One Research Article Biliary tract cancer (BTC) is often difficult to diagnose definitively, even through histological examination. MicroRNAs (miRNAs) regulate a variety of physiological processes. In recent years, it has been suggested that profiles for circulating miRNAs, as well as those for tissue miRNAs, have the potential to be used as diagnostic biomarkers for cancer. The aim of this study was to confirm the existence of miRNAs in human bile and to assess their potential as clinical biomarkers for BTC. We sampled bile from patients who underwent biliary drainage for biliary diseases such as BTC and choledocholithiasis. PCR-based miRNA detection and miRNA cloning were performed to identify bile miRNAs. Using high-throughput real-time PCR-based miRNA microarrays, the expression profiles of 667 miRNAs were compared in patients with malignant disease (n = 9) and age-matched patients with the benign disease choledocholithiasis (n = 9). We subsequently characterized bile miRNAs in terms of stability and localization. Through cloning and using PCR methods, we confirmed that miRNAs exist in bile. Differential analysis of bile miRNAs demonstrated that 10 of the 667 miRNAs were significantly more highly expressed in the malignant group than in the benign group at P<0.0005. Setting the specificity threshold to 100% showed that some miRNAs (miR-9, miR-302c*, miR-199a-3p and miR-222*) had a sensitivity level of 88.9%, and receiver-operating characteristic analysis demonstrated that miR-9 and miR-145* could be useful diagnostic markers for BTC. Moreover, we verified the long-term stability of miRNAs in bile, a characteristic that makes them suitable for diagnostic use in clinical settings. We also confirmed that bile miRNAs are localized to the malignant/benign biliary epithelia. These findings suggest that bile miRNAs could be informative biomarkers for hepatobiliary disease and that some miRNAs, particularly miR-9, may be helpful in the diagnosis and clinical management of BTC. Public Library of Science 2011-08-17 /pmc/articles/PMC3157401/ /pubmed/21858175 http://dx.doi.org/10.1371/journal.pone.0023584 Text en Shigehara 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
Shigehara, Kengo
Yokomuro, Shigeki
Ishibashi, Osamu
Mizuguchi, Yoshiaki
Arima, Yasuo
Kawahigashi, Yutaka
Kanda, Tomohiro
Akagi, Ichiro
Tajiri, Takashi
Yoshida, Hiroshi
Takizawa, Toshihiro
Uchida, Eiji
Real-Time PCR-Based Analysis of the Human Bile MicroRNAome Identifies miR-9 as a Potential Diagnostic Biomarker for Biliary Tract Cancer
title Real-Time PCR-Based Analysis of the Human Bile MicroRNAome Identifies miR-9 as a Potential Diagnostic Biomarker for Biliary Tract Cancer
title_full Real-Time PCR-Based Analysis of the Human Bile MicroRNAome Identifies miR-9 as a Potential Diagnostic Biomarker for Biliary Tract Cancer
title_fullStr Real-Time PCR-Based Analysis of the Human Bile MicroRNAome Identifies miR-9 as a Potential Diagnostic Biomarker for Biliary Tract Cancer
title_full_unstemmed Real-Time PCR-Based Analysis of the Human Bile MicroRNAome Identifies miR-9 as a Potential Diagnostic Biomarker for Biliary Tract Cancer
title_short Real-Time PCR-Based Analysis of the Human Bile MicroRNAome Identifies miR-9 as a Potential Diagnostic Biomarker for Biliary Tract Cancer
title_sort real-time pcr-based analysis of the human bile micrornaome identifies mir-9 as a potential diagnostic biomarker for biliary tract cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157401/
https://www.ncbi.nlm.nih.gov/pubmed/21858175
http://dx.doi.org/10.1371/journal.pone.0023584
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