Gene Expression and DNA Methylation Status of Glutathione S-Transferase Mu1 and Mu5 in Urothelial Carcinoma.

Bladder cancer is highly recurrent after therapy, which has an enormous impact on the health and financial condition of the patient. It is worth developing diagnostic tools for bladder cancer. In our previous study, we found that the bladder carcinogen BBN increased urothelial global DNA CpG methyla...

Full description

Bibliographic Details
Main Authors: Shou-Chieh Wang, Chin-Chin Huang, Cheng-Huang Shen, Lei-Chen Lin, Pei-Wen Zhao, Shih-Ying Chen, Yu-Chiao Deng, Yi-Wen Liu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4942074?pdf=render
_version_ 1828370235147681792
author Shou-Chieh Wang
Chin-Chin Huang
Cheng-Huang Shen
Lei-Chen Lin
Pei-Wen Zhao
Shih-Ying Chen
Yu-Chiao Deng
Yi-Wen Liu
author_facet Shou-Chieh Wang
Chin-Chin Huang
Cheng-Huang Shen
Lei-Chen Lin
Pei-Wen Zhao
Shih-Ying Chen
Yu-Chiao Deng
Yi-Wen Liu
author_sort Shou-Chieh Wang
collection DOAJ
description Bladder cancer is highly recurrent after therapy, which has an enormous impact on the health and financial condition of the patient. It is worth developing diagnostic tools for bladder cancer. In our previous study, we found that the bladder carcinogen BBN increased urothelial global DNA CpG methylation and decreased GSTM1 protein expression in mice. Here, the correlation of BBN-decreased GSTM1 and GSTM gene CpG methylation status was analyzed in mice bladders. BBN treatment decreased the protein and mRNA expression of GSTM1, and the CpG methylation ratio of GSTM1 gene promoter was slightly increased in mice bladders. Unlike mouse GSTM1, the human GSTM1 gene tends to be deleted in bladder cancers. Among 7 human bladder cancer cell lines, GSTM1 gene is really null in 6 cell lines except one, T24 cells. The CpG methylation level of GSTM1 was 9.9% and 5-aza-dC did not significantly increase GSTM1 protein and mRNA expression in T24 cells; however, the GSTM5 gene was CpG hypermethylated (65.4%) and 5-aza-dC also did not affect the methylation ratio and mRNA expression. However, in other cell lines without GSTM1, 5-aza-dC increased GSTM5 expression and decreased its CpG DNA methylation ratio from 84.6% to 61.5% in 5637, and from 97.4% to 75% in J82 cells. In summary, two biomarkers of bladder tumor were provided. One is the GSTM1 gene which is down-regulated in mice bladder carcinogenesis and is usually deleted in human urothelial carcinoma, while the other is the GSTM5 gene, which is inactivated by DNA CpG methylation.
first_indexed 2024-04-14T06:36:20Z
format Article
id doaj.art-4244df29c83e40ee86f97949dbf1dab5
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-04-14T06:36:20Z
publishDate 2016-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-4244df29c83e40ee86f97949dbf1dab52022-12-22T02:07:28ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01117e015910210.1371/journal.pone.0159102Gene Expression and DNA Methylation Status of Glutathione S-Transferase Mu1 and Mu5 in Urothelial Carcinoma.Shou-Chieh WangChin-Chin HuangCheng-Huang ShenLei-Chen LinPei-Wen ZhaoShih-Ying ChenYu-Chiao DengYi-Wen LiuBladder cancer is highly recurrent after therapy, which has an enormous impact on the health and financial condition of the patient. It is worth developing diagnostic tools for bladder cancer. In our previous study, we found that the bladder carcinogen BBN increased urothelial global DNA CpG methylation and decreased GSTM1 protein expression in mice. Here, the correlation of BBN-decreased GSTM1 and GSTM gene CpG methylation status was analyzed in mice bladders. BBN treatment decreased the protein and mRNA expression of GSTM1, and the CpG methylation ratio of GSTM1 gene promoter was slightly increased in mice bladders. Unlike mouse GSTM1, the human GSTM1 gene tends to be deleted in bladder cancers. Among 7 human bladder cancer cell lines, GSTM1 gene is really null in 6 cell lines except one, T24 cells. The CpG methylation level of GSTM1 was 9.9% and 5-aza-dC did not significantly increase GSTM1 protein and mRNA expression in T24 cells; however, the GSTM5 gene was CpG hypermethylated (65.4%) and 5-aza-dC also did not affect the methylation ratio and mRNA expression. However, in other cell lines without GSTM1, 5-aza-dC increased GSTM5 expression and decreased its CpG DNA methylation ratio from 84.6% to 61.5% in 5637, and from 97.4% to 75% in J82 cells. In summary, two biomarkers of bladder tumor were provided. One is the GSTM1 gene which is down-regulated in mice bladder carcinogenesis and is usually deleted in human urothelial carcinoma, while the other is the GSTM5 gene, which is inactivated by DNA CpG methylation.http://europepmc.org/articles/PMC4942074?pdf=render
spellingShingle Shou-Chieh Wang
Chin-Chin Huang
Cheng-Huang Shen
Lei-Chen Lin
Pei-Wen Zhao
Shih-Ying Chen
Yu-Chiao Deng
Yi-Wen Liu
Gene Expression and DNA Methylation Status of Glutathione S-Transferase Mu1 and Mu5 in Urothelial Carcinoma.
PLoS ONE
title Gene Expression and DNA Methylation Status of Glutathione S-Transferase Mu1 and Mu5 in Urothelial Carcinoma.
title_full Gene Expression and DNA Methylation Status of Glutathione S-Transferase Mu1 and Mu5 in Urothelial Carcinoma.
title_fullStr Gene Expression and DNA Methylation Status of Glutathione S-Transferase Mu1 and Mu5 in Urothelial Carcinoma.
title_full_unstemmed Gene Expression and DNA Methylation Status of Glutathione S-Transferase Mu1 and Mu5 in Urothelial Carcinoma.
title_short Gene Expression and DNA Methylation Status of Glutathione S-Transferase Mu1 and Mu5 in Urothelial Carcinoma.
title_sort gene expression and dna methylation status of glutathione s transferase mu1 and mu5 in urothelial carcinoma
url http://europepmc.org/articles/PMC4942074?pdf=render
work_keys_str_mv AT shouchiehwang geneexpressionanddnamethylationstatusofglutathionestransferasemu1andmu5inurothelialcarcinoma
AT chinchinhuang geneexpressionanddnamethylationstatusofglutathionestransferasemu1andmu5inurothelialcarcinoma
AT chenghuangshen geneexpressionanddnamethylationstatusofglutathionestransferasemu1andmu5inurothelialcarcinoma
AT leichenlin geneexpressionanddnamethylationstatusofglutathionestransferasemu1andmu5inurothelialcarcinoma
AT peiwenzhao geneexpressionanddnamethylationstatusofglutathionestransferasemu1andmu5inurothelialcarcinoma
AT shihyingchen geneexpressionanddnamethylationstatusofglutathionestransferasemu1andmu5inurothelialcarcinoma
AT yuchiaodeng geneexpressionanddnamethylationstatusofglutathionestransferasemu1andmu5inurothelialcarcinoma
AT yiwenliu geneexpressionanddnamethylationstatusofglutathionestransferasemu1andmu5inurothelialcarcinoma