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Cell-free microRNA expression signatures in urine serve as novel noninvasive biomarkers for diagnosis and recurrence prediction of bladder cancer

Urinary microRNAs (miRNAs) are potential biomarkers for the noninvasive diagnosis of bladder cancer (BC). In this study, we aimed to develop a urinary miRNAs panel for diagnosing and predicting recurrence of BC. Genome-wide miRNAs analysis by deep sequencing followed by two phases of quantitative re...

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Autores principales: Du, Lutao, Jiang, Xiumei, Duan, Weili, Wang, Rui, Wang, lishui, Zheng, Guixi, Yan, Keqiang, Wang, Lili, Li, Juan, Zhang, Xin, Pan, Hongwei, Yang, Yongmei, Wang, Chuanxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522322/
https://www.ncbi.nlm.nih.gov/pubmed/28388561
http://dx.doi.org/10.18632/oncotarget.16586
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author Du, Lutao
Jiang, Xiumei
Duan, Weili
Wang, Rui
Wang, lishui
Zheng, Guixi
Yan, Keqiang
Wang, Lili
Li, Juan
Zhang, Xin
Pan, Hongwei
Yang, Yongmei
Wang, Chuanxin
author_facet Du, Lutao
Jiang, Xiumei
Duan, Weili
Wang, Rui
Wang, lishui
Zheng, Guixi
Yan, Keqiang
Wang, Lili
Li, Juan
Zhang, Xin
Pan, Hongwei
Yang, Yongmei
Wang, Chuanxin
author_sort Du, Lutao
collection PubMed
description Urinary microRNAs (miRNAs) are potential biomarkers for the noninvasive diagnosis of bladder cancer (BC). In this study, we aimed to develop a urinary miRNAs panel for diagnosing and predicting recurrence of BC. Genome-wide miRNAs analysis by deep sequencing followed by two phases of quantitative real-time PCR assays were performed on urine supernatant of 276 BC patients and 276 controls. We identified a seven-miRNA panel (miR-7-5p, miR-22-3p, miR-29a-3p, miR-126-5p, miR-200a-3p, miR-375, and miR-423-5p) that provided high diagnostic accuracy of BC with an AUC of 0.923 and 0.916 in training and validation set, respectively. The corresponding AUCs of this panel for Ta, T1 and T2-T4 were 0.864, 0.930 and 0.978, significantly higher than those of urine cytology, which were 0.531, 0.628 and 0.724, respectively (all p < 0.05). Moreover, Kaplan–Meier analysis showed that nonmuscle-invasive BC (NMIBC) patients with high miR-22-3p and low miR-200a-3p level had worse recurrence-free survival (RFS) (p = 0.002 and 0.040, respectively). Multivariate Cox regression analysis revealed that miR-22-3p and miR-200a-3p were independently associated with RFS of NMIBC (p = 0.024 and 0.008, respectively). In conclusion, our results suggested that urinary miRNAs may have considerable clinical value in diagnosis and recurrence prediction of BC.
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spelling pubmed-55223222017-08-21 Cell-free microRNA expression signatures in urine serve as novel noninvasive biomarkers for diagnosis and recurrence prediction of bladder cancer Du, Lutao Jiang, Xiumei Duan, Weili Wang, Rui Wang, lishui Zheng, Guixi Yan, Keqiang Wang, Lili Li, Juan Zhang, Xin Pan, Hongwei Yang, Yongmei Wang, Chuanxin Oncotarget Research Paper Urinary microRNAs (miRNAs) are potential biomarkers for the noninvasive diagnosis of bladder cancer (BC). In this study, we aimed to develop a urinary miRNAs panel for diagnosing and predicting recurrence of BC. Genome-wide miRNAs analysis by deep sequencing followed by two phases of quantitative real-time PCR assays were performed on urine supernatant of 276 BC patients and 276 controls. We identified a seven-miRNA panel (miR-7-5p, miR-22-3p, miR-29a-3p, miR-126-5p, miR-200a-3p, miR-375, and miR-423-5p) that provided high diagnostic accuracy of BC with an AUC of 0.923 and 0.916 in training and validation set, respectively. The corresponding AUCs of this panel for Ta, T1 and T2-T4 were 0.864, 0.930 and 0.978, significantly higher than those of urine cytology, which were 0.531, 0.628 and 0.724, respectively (all p < 0.05). Moreover, Kaplan–Meier analysis showed that nonmuscle-invasive BC (NMIBC) patients with high miR-22-3p and low miR-200a-3p level had worse recurrence-free survival (RFS) (p = 0.002 and 0.040, respectively). Multivariate Cox regression analysis revealed that miR-22-3p and miR-200a-3p were independently associated with RFS of NMIBC (p = 0.024 and 0.008, respectively). In conclusion, our results suggested that urinary miRNAs may have considerable clinical value in diagnosis and recurrence prediction of BC. Impact Journals LLC 2017-03-28 /pmc/articles/PMC5522322/ /pubmed/28388561 http://dx.doi.org/10.18632/oncotarget.16586 Text en Copyright: © 2017 Du et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Du, Lutao
Jiang, Xiumei
Duan, Weili
Wang, Rui
Wang, lishui
Zheng, Guixi
Yan, Keqiang
Wang, Lili
Li, Juan
Zhang, Xin
Pan, Hongwei
Yang, Yongmei
Wang, Chuanxin
Cell-free microRNA expression signatures in urine serve as novel noninvasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title Cell-free microRNA expression signatures in urine serve as novel noninvasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_full Cell-free microRNA expression signatures in urine serve as novel noninvasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_fullStr Cell-free microRNA expression signatures in urine serve as novel noninvasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_full_unstemmed Cell-free microRNA expression signatures in urine serve as novel noninvasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_short Cell-free microRNA expression signatures in urine serve as novel noninvasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_sort cell-free microrna expression signatures in urine serve as novel noninvasive biomarkers for diagnosis and recurrence prediction of bladder cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522322/
https://www.ncbi.nlm.nih.gov/pubmed/28388561
http://dx.doi.org/10.18632/oncotarget.16586
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