Connexin 26 is Down-Regulated by KDM5B in the Progression of Bladder Cancer

Connexin 26 (Cx26) expression is down-regulated and KDM5B (H3K4 demethylase) is up-regulated in the progression of bladder cancer, suggesting that Cx26 expression may be down-regulated by KDM5B in bladder cancer. To test the hypothesis, the HT1376 and T24 human bladder carcinoma cells were transfect...

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Main Authors: Enqing Xiong, Bo Song, Zhansong Zhou, Jinhong Pan, Yongping Su, Xin Li, Zhiwen Chen
Format: Article
Language:English
Published: MDPI AG 2013-04-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/14/4/7866
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spelling doaj-3f017d3d989843948e47afc1ba9e60c62020-11-25T00:14:39ZengMDPI AGInternational Journal of Molecular Sciences1422-00672013-04-011447866787910.3390/ijms14047866Connexin 26 is Down-Regulated by KDM5B in the Progression of Bladder CancerEnqing XiongBo SongZhansong ZhouJinhong PanYongping SuXin LiZhiwen ChenConnexin 26 (Cx26) expression is down-regulated and KDM5B (H3K4 demethylase) is up-regulated in the progression of bladder cancer, suggesting that Cx26 expression may be down-regulated by KDM5B in bladder cancer. To test the hypothesis, the HT1376 and T24 human bladder carcinoma cells were transfected with the plasmids pcDNA3.1-KDM5B, and caused the down-regulation of Cx26 expression. In contrast, the HT1376 and T24 cells transfected with the plasmids pTZU6+1-shRNA-KDM5B1 and pTZU6+1-shRNA-KDM5B2 caused the up-regulation of Cx26 expression. Immunohistochemistry and Spearman’s rank correlation analysis showed that the immunohistochemical expression of KDM5B and Cx26 was inversely related in bladder carcinoma tissues but no relationship in benign tissues. Taken together, these results indicate that KDM5B represses Cx26 expression in the bladder cancer development. Thus, a negative value to Cx26 immunohistochemical expression and a positive value to KDM5B immunohistochemical expression could be an ancillary diagnosis of primary bladder malignancy.http://www.mdpi.com/1422-0067/14/4/7866KDM5Bconnexin 26HT1376 human bladder cancer cellsT24 human bladder cancer cellsreal-time qPCRimmunohistochemistryspearman’s rank correlation
collection DOAJ
language English
format Article
sources DOAJ
author Enqing Xiong
Bo Song
Zhansong Zhou
Jinhong Pan
Yongping Su
Xin Li
Zhiwen Chen
spellingShingle Enqing Xiong
Bo Song
Zhansong Zhou
Jinhong Pan
Yongping Su
Xin Li
Zhiwen Chen
Connexin 26 is Down-Regulated by KDM5B in the Progression of Bladder Cancer
International Journal of Molecular Sciences
KDM5B
connexin 26
HT1376 human bladder cancer cells
T24 human bladder cancer cells
real-time qPCR
immunohistochemistry
spearman’s rank correlation
author_facet Enqing Xiong
Bo Song
Zhansong Zhou
Jinhong Pan
Yongping Su
Xin Li
Zhiwen Chen
author_sort Enqing Xiong
title Connexin 26 is Down-Regulated by KDM5B in the Progression of Bladder Cancer
title_short Connexin 26 is Down-Regulated by KDM5B in the Progression of Bladder Cancer
title_full Connexin 26 is Down-Regulated by KDM5B in the Progression of Bladder Cancer
title_fullStr Connexin 26 is Down-Regulated by KDM5B in the Progression of Bladder Cancer
title_full_unstemmed Connexin 26 is Down-Regulated by KDM5B in the Progression of Bladder Cancer
title_sort connexin 26 is down-regulated by kdm5b in the progression of bladder cancer
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2013-04-01
description Connexin 26 (Cx26) expression is down-regulated and KDM5B (H3K4 demethylase) is up-regulated in the progression of bladder cancer, suggesting that Cx26 expression may be down-regulated by KDM5B in bladder cancer. To test the hypothesis, the HT1376 and T24 human bladder carcinoma cells were transfected with the plasmids pcDNA3.1-KDM5B, and caused the down-regulation of Cx26 expression. In contrast, the HT1376 and T24 cells transfected with the plasmids pTZU6+1-shRNA-KDM5B1 and pTZU6+1-shRNA-KDM5B2 caused the up-regulation of Cx26 expression. Immunohistochemistry and Spearman’s rank correlation analysis showed that the immunohistochemical expression of KDM5B and Cx26 was inversely related in bladder carcinoma tissues but no relationship in benign tissues. Taken together, these results indicate that KDM5B represses Cx26 expression in the bladder cancer development. Thus, a negative value to Cx26 immunohistochemical expression and a positive value to KDM5B immunohistochemical expression could be an ancillary diagnosis of primary bladder malignancy.
topic KDM5B
connexin 26
HT1376 human bladder cancer cells
T24 human bladder cancer cells
real-time qPCR
immunohistochemistry
spearman’s rank correlation
url http://www.mdpi.com/1422-0067/14/4/7866
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