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A potential panel of five mRNAs in urinary extracellular vesicles for the detection of bladder cancer

BACKGROUND: Extracellular vesicles (EVs) have showed promising potential in liquid biopsy of cancer. In present study, we evaluate the feasibility to diagnose bladder cancer using EVs RNA markers identified from public tissue RNA sequencing data. METHODS: We used urine samples from a cohort of popul...

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Autores principales: Xu, Yong, Zhang, Peng, Tan, Yizhou, Jia, Zhuo, Chen, Guangfu, Niu, Yinong, Xiao, Jing, Sun, Shengkun, Zhang, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947455/
https://www.ncbi.nlm.nih.gov/pubmed/33718082
http://dx.doi.org/10.21037/tau-20-1057
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author Xu, Yong
Zhang, Peng
Tan, Yizhou
Jia, Zhuo
Chen, Guangfu
Niu, Yinong
Xiao, Jing
Sun, Shengkun
Zhang, Xu
author_facet Xu, Yong
Zhang, Peng
Tan, Yizhou
Jia, Zhuo
Chen, Guangfu
Niu, Yinong
Xiao, Jing
Sun, Shengkun
Zhang, Xu
author_sort Xu, Yong
collection PubMed
description BACKGROUND: Extracellular vesicles (EVs) have showed promising potential in liquid biopsy of cancer. In present study, we evaluate the feasibility to diagnose bladder cancer using EVs RNA markers identified from public tissue RNA sequencing data. METHODS: We used urine samples from a cohort of population with suspected bladder cancer. Disease status (i.e., primary or recurrent bladder cancer) was diagnosed by cystoscopy. A prediction model including the expression of multiple RNAs in urinary EVs were developed in training cohort (n=368, 126 bladder cancer and 242 negative controls). The performance of optimal model (ExoPanel) consists of five mRNAs (MYBL2, TK1, UBE2C, KRT7, S100A2) was further assessed by a validation cohort (n=155, 56 bladder cancer and 99 negative controls). RESULTS: The performance of ExoPanel in training cohort was AUC 0.7759 (95% CI: 0.7259–0.8260), NPV 90.34% (95% CI: 84.04–94.42%), SN 88.89% (95% CI: 81.75–93.57%), and SP 54.13% (95% CI: 47.63–60.50%) respectively. In the validation cohort, the performance of this model was AUC 0.8402 (95% CI: 0.7690–0.9114), NPV 90.91% (95% CI: 79.29–96.60%), SN 91.07% (95% CI: 79.63–96.67%), and SP 50.51% (95% CI: 40.34–60.63%). Using this model, it is possible to rule out a significant number of non cancer patients, thus reduce the unnecessary operation of cystoscopy. CONCLUSIONS: We discovered a panel of five mRNAs, and evaluated its potential to facilitate bladder cancer diagnosis by analyzing their expression in urinary EVs.
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spelling pubmed-79474552021-03-12 A potential panel of five mRNAs in urinary extracellular vesicles for the detection of bladder cancer Xu, Yong Zhang, Peng Tan, Yizhou Jia, Zhuo Chen, Guangfu Niu, Yinong Xiao, Jing Sun, Shengkun Zhang, Xu Transl Androl Urol Original Article BACKGROUND: Extracellular vesicles (EVs) have showed promising potential in liquid biopsy of cancer. In present study, we evaluate the feasibility to diagnose bladder cancer using EVs RNA markers identified from public tissue RNA sequencing data. METHODS: We used urine samples from a cohort of population with suspected bladder cancer. Disease status (i.e., primary or recurrent bladder cancer) was diagnosed by cystoscopy. A prediction model including the expression of multiple RNAs in urinary EVs were developed in training cohort (n=368, 126 bladder cancer and 242 negative controls). The performance of optimal model (ExoPanel) consists of five mRNAs (MYBL2, TK1, UBE2C, KRT7, S100A2) was further assessed by a validation cohort (n=155, 56 bladder cancer and 99 negative controls). RESULTS: The performance of ExoPanel in training cohort was AUC 0.7759 (95% CI: 0.7259–0.8260), NPV 90.34% (95% CI: 84.04–94.42%), SN 88.89% (95% CI: 81.75–93.57%), and SP 54.13% (95% CI: 47.63–60.50%) respectively. In the validation cohort, the performance of this model was AUC 0.8402 (95% CI: 0.7690–0.9114), NPV 90.91% (95% CI: 79.29–96.60%), SN 91.07% (95% CI: 79.63–96.67%), and SP 50.51% (95% CI: 40.34–60.63%). Using this model, it is possible to rule out a significant number of non cancer patients, thus reduce the unnecessary operation of cystoscopy. CONCLUSIONS: We discovered a panel of five mRNAs, and evaluated its potential to facilitate bladder cancer diagnosis by analyzing their expression in urinary EVs. AME Publishing Company 2021-02 /pmc/articles/PMC7947455/ /pubmed/33718082 http://dx.doi.org/10.21037/tau-20-1057 Text en 2021 Translational Andrology and Urology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Xu, Yong
Zhang, Peng
Tan, Yizhou
Jia, Zhuo
Chen, Guangfu
Niu, Yinong
Xiao, Jing
Sun, Shengkun
Zhang, Xu
A potential panel of five mRNAs in urinary extracellular vesicles for the detection of bladder cancer
title A potential panel of five mRNAs in urinary extracellular vesicles for the detection of bladder cancer
title_full A potential panel of five mRNAs in urinary extracellular vesicles for the detection of bladder cancer
title_fullStr A potential panel of five mRNAs in urinary extracellular vesicles for the detection of bladder cancer
title_full_unstemmed A potential panel of five mRNAs in urinary extracellular vesicles for the detection of bladder cancer
title_short A potential panel of five mRNAs in urinary extracellular vesicles for the detection of bladder cancer
title_sort potential panel of five mrnas in urinary extracellular vesicles for the detection of bladder cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7947455/
https://www.ncbi.nlm.nih.gov/pubmed/33718082
http://dx.doi.org/10.21037/tau-20-1057
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