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Cell‐free lncRNA expression signatures in urine serve as novel non‐invasive biomarkers for diagnosis and recurrence prediction of bladder cancer

Cell‐free long non‐coding RNAs (lncRNAs) are stably present in urine and can serve as non‐invasive biomarkers for cancer. We aimed to identify signatures of lncRNAs in urine for diagnosis and prognosis of bladder cancer (BC). Screening of lncRNAs by microarray analysis was performed using urine samp...

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Detalles Bibliográficos
Autores principales: Du, Lutao, Duan, Weili, Jiang, Xiumei, Zhao, Li, Li, Juan, Wang, Rui, Yan, Suzhen, Xie, Yujiao, Yan, Keqiang, Wang, Qingliang, Wang, Lili, Yang, Yongmei, Wang, Chuanxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908122/
https://www.ncbi.nlm.nih.gov/pubmed/29516641
http://dx.doi.org/10.1111/jcmm.13578
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author Du, Lutao
Duan, Weili
Jiang, Xiumei
Zhao, Li
Li, Juan
Wang, Rui
Yan, Suzhen
Xie, Yujiao
Yan, Keqiang
Wang, Qingliang
Wang, Lili
Yang, Yongmei
Wang, Chuanxin
author_facet Du, Lutao
Duan, Weili
Jiang, Xiumei
Zhao, Li
Li, Juan
Wang, Rui
Yan, Suzhen
Xie, Yujiao
Yan, Keqiang
Wang, Qingliang
Wang, Lili
Yang, Yongmei
Wang, Chuanxin
author_sort Du, Lutao
collection PubMed
description Cell‐free long non‐coding RNAs (lncRNAs) are stably present in urine and can serve as non‐invasive biomarkers for cancer. We aimed to identify signatures of lncRNAs in urine for diagnosis and prognosis of bladder cancer (BC). Screening of lncRNAs by microarray analysis was performed using urine samples of 10 BC patients and 10 controls. Expressions of candidate lncRNAs were evaluated in the training and validation set including 230 BC patients and 230 controls by quantitative reverse transcription polymerase chain reaction (qRT‐PCR). A two‐lncRNA panel (uc004cox.4 and GAS5) was constructed and provided high diagnostic accuracy of BC with an area under the curve (AUC) of 0.885 (95% CI, 0.836‐0.924). The AUCs of the lncRNA panel for Ta, T1 and T2‐T4 were 0.843, 0.867 and 0.923, respectively, significantly higher than those of urine cytology (all P < .05). Kaplan‐Meier analysis revealed that higher level of uc004cox.4 was associated with poor recurrence‐free survival (RFS) of non‐muscle invasive BC (NMIBC) (P = .008). Additionally, Cox regression analysis indicated that uc004cox.4 was an independent prognostic factor for RFS of NMIBC (P = .018). Taken together, our findings indicated that urinary lncRNA signatures possessed potential clinical value for BC diagnosis. Moreover, uc004cox.4 could provide prognostic information for NMIBC.
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spelling pubmed-59081222018-05-03 Cell‐free lncRNA expression signatures in urine serve as novel non‐invasive biomarkers for diagnosis and recurrence prediction of bladder cancer Du, Lutao Duan, Weili Jiang, Xiumei Zhao, Li Li, Juan Wang, Rui Yan, Suzhen Xie, Yujiao Yan, Keqiang Wang, Qingliang Wang, Lili Yang, Yongmei Wang, Chuanxin J Cell Mol Med Original Articles Cell‐free long non‐coding RNAs (lncRNAs) are stably present in urine and can serve as non‐invasive biomarkers for cancer. We aimed to identify signatures of lncRNAs in urine for diagnosis and prognosis of bladder cancer (BC). Screening of lncRNAs by microarray analysis was performed using urine samples of 10 BC patients and 10 controls. Expressions of candidate lncRNAs were evaluated in the training and validation set including 230 BC patients and 230 controls by quantitative reverse transcription polymerase chain reaction (qRT‐PCR). A two‐lncRNA panel (uc004cox.4 and GAS5) was constructed and provided high diagnostic accuracy of BC with an area under the curve (AUC) of 0.885 (95% CI, 0.836‐0.924). The AUCs of the lncRNA panel for Ta, T1 and T2‐T4 were 0.843, 0.867 and 0.923, respectively, significantly higher than those of urine cytology (all P < .05). Kaplan‐Meier analysis revealed that higher level of uc004cox.4 was associated with poor recurrence‐free survival (RFS) of non‐muscle invasive BC (NMIBC) (P = .008). Additionally, Cox regression analysis indicated that uc004cox.4 was an independent prognostic factor for RFS of NMIBC (P = .018). Taken together, our findings indicated that urinary lncRNA signatures possessed potential clinical value for BC diagnosis. Moreover, uc004cox.4 could provide prognostic information for NMIBC. John Wiley and Sons Inc. 2018-03-08 2018-05 /pmc/articles/PMC5908122/ /pubmed/29516641 http://dx.doi.org/10.1111/jcmm.13578 Text en © 2018 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Du, Lutao
Duan, Weili
Jiang, Xiumei
Zhao, Li
Li, Juan
Wang, Rui
Yan, Suzhen
Xie, Yujiao
Yan, Keqiang
Wang, Qingliang
Wang, Lili
Yang, Yongmei
Wang, Chuanxin
Cell‐free lncRNA expression signatures in urine serve as novel non‐invasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title Cell‐free lncRNA expression signatures in urine serve as novel non‐invasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_full Cell‐free lncRNA expression signatures in urine serve as novel non‐invasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_fullStr Cell‐free lncRNA expression signatures in urine serve as novel non‐invasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_full_unstemmed Cell‐free lncRNA expression signatures in urine serve as novel non‐invasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_short Cell‐free lncRNA expression signatures in urine serve as novel non‐invasive biomarkers for diagnosis and recurrence prediction of bladder cancer
title_sort cell‐free lncrna expression signatures in urine serve as novel non‐invasive biomarkers for diagnosis and recurrence prediction of bladder cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908122/
https://www.ncbi.nlm.nih.gov/pubmed/29516641
http://dx.doi.org/10.1111/jcmm.13578
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