MicroRNA expression signatures of bladder cancer revealed by deep sequencing.

MicroRNAs (miRNAs) are a class of small noncoding RNAs that regulate gene expression. They are aberrantly expressed in many types of cancers. In this study, we determined the genome-wide miRNA profiles in bladder urothelial carcinoma by deep sequencing.We detected 656 differentially expressed known...

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Main Authors: Yonghua Han, Jiahao Chen, Xiaokun Zhao, Chaozhao Liang, Yong Wang, Liang Sun, Zhimao Jiang, Zhongfu Zhang, Ruilin Yang, Jing Chen, Zesong Li, Aifa Tang, Xianxin Li, Jiongxian Ye, Zhichen Guan, Yaoting Gui, Zhiming Cai
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-03-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3065473?pdf=render
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spelling doaj-e7aa983adb3b45b18f0d1d2a9e81a1192020-11-24T21:30:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-03-0163e1828610.1371/journal.pone.0018286MicroRNA expression signatures of bladder cancer revealed by deep sequencing.Yonghua HanJiahao ChenXiaokun ZhaoChaozhao LiangYong WangLiang SunZhimao JiangZhongfu ZhangRuilin YangJing ChenZesong LiAifa TangXianxin LiJiongxian YeZhichen GuanYaoting GuiZhiming CaiMicroRNAs (miRNAs) are a class of small noncoding RNAs that regulate gene expression. They are aberrantly expressed in many types of cancers. In this study, we determined the genome-wide miRNA profiles in bladder urothelial carcinoma by deep sequencing.We detected 656 differentially expressed known human miRNAs and miRNA antisense sequences (miRNA*s) in nine bladder urothelial carcinoma patients by deep sequencing. Many miRNAs and miRNA*s were significantly upregulated or downregulated in bladder urothelial carcinoma compared to matched histologically normal urothelium. hsa-miR-96 was the most significantly upregulated miRNA and hsa-miR-490-5p was the most significantly downregulated one. Upregulated miRNAs were more common than downregulated ones. The hsa-miR-183, hsa-miR-200b ∼ 429, hsa-miR-200c ∼ 141 and hsa-miR-17 ∼ 92 clusters were significantly upregulated. The hsa-miR-143 ∼ 145 cluster was significantly downregulated. hsa-miR-182, hsa-miR-183, hsa-miR-200a, hsa-miR-143 and hsa-miR-195 were evaluated by Real-Time qPCR in a total of fifty-one bladder urothelial carcinoma patients. They were aberrantly expressed in bladder urothelial carcinoma compared to matched histologically normal urothelium (p < 0.001 for each miRNA).To date, this is the first study to determine genome-wide miRNA expression patterns in human bladder urothelial carcinoma by deep sequencing. We found that a collection of miRNAs were aberrantly expressed in bladder urothelial carcinoma compared to matched histologically normal urothelium, suggesting that they might play roles as oncogenes or tumor suppressors in the development and/or progression of this cancer. Our data provide novel insights into cancer biology.http://europepmc.org/articles/PMC3065473?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yonghua Han
Jiahao Chen
Xiaokun Zhao
Chaozhao Liang
Yong Wang
Liang Sun
Zhimao Jiang
Zhongfu Zhang
Ruilin Yang
Jing Chen
Zesong Li
Aifa Tang
Xianxin Li
Jiongxian Ye
Zhichen Guan
Yaoting Gui
Zhiming Cai
spellingShingle Yonghua Han
Jiahao Chen
Xiaokun Zhao
Chaozhao Liang
Yong Wang
Liang Sun
Zhimao Jiang
Zhongfu Zhang
Ruilin Yang
Jing Chen
Zesong Li
Aifa Tang
Xianxin Li
Jiongxian Ye
Zhichen Guan
Yaoting Gui
Zhiming Cai
MicroRNA expression signatures of bladder cancer revealed by deep sequencing.
PLoS ONE
author_facet Yonghua Han
Jiahao Chen
Xiaokun Zhao
Chaozhao Liang
Yong Wang
Liang Sun
Zhimao Jiang
Zhongfu Zhang
Ruilin Yang
Jing Chen
Zesong Li
Aifa Tang
Xianxin Li
Jiongxian Ye
Zhichen Guan
Yaoting Gui
Zhiming Cai
author_sort Yonghua Han
title MicroRNA expression signatures of bladder cancer revealed by deep sequencing.
title_short MicroRNA expression signatures of bladder cancer revealed by deep sequencing.
title_full MicroRNA expression signatures of bladder cancer revealed by deep sequencing.
title_fullStr MicroRNA expression signatures of bladder cancer revealed by deep sequencing.
title_full_unstemmed MicroRNA expression signatures of bladder cancer revealed by deep sequencing.
title_sort microrna expression signatures of bladder cancer revealed by deep sequencing.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-03-01
description MicroRNAs (miRNAs) are a class of small noncoding RNAs that regulate gene expression. They are aberrantly expressed in many types of cancers. In this study, we determined the genome-wide miRNA profiles in bladder urothelial carcinoma by deep sequencing.We detected 656 differentially expressed known human miRNAs and miRNA antisense sequences (miRNA*s) in nine bladder urothelial carcinoma patients by deep sequencing. Many miRNAs and miRNA*s were significantly upregulated or downregulated in bladder urothelial carcinoma compared to matched histologically normal urothelium. hsa-miR-96 was the most significantly upregulated miRNA and hsa-miR-490-5p was the most significantly downregulated one. Upregulated miRNAs were more common than downregulated ones. The hsa-miR-183, hsa-miR-200b ∼ 429, hsa-miR-200c ∼ 141 and hsa-miR-17 ∼ 92 clusters were significantly upregulated. The hsa-miR-143 ∼ 145 cluster was significantly downregulated. hsa-miR-182, hsa-miR-183, hsa-miR-200a, hsa-miR-143 and hsa-miR-195 were evaluated by Real-Time qPCR in a total of fifty-one bladder urothelial carcinoma patients. They were aberrantly expressed in bladder urothelial carcinoma compared to matched histologically normal urothelium (p < 0.001 for each miRNA).To date, this is the first study to determine genome-wide miRNA expression patterns in human bladder urothelial carcinoma by deep sequencing. We found that a collection of miRNAs were aberrantly expressed in bladder urothelial carcinoma compared to matched histologically normal urothelium, suggesting that they might play roles as oncogenes or tumor suppressors in the development and/or progression of this cancer. Our data provide novel insights into cancer biology.
url http://europepmc.org/articles/PMC3065473?pdf=render
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