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Mapping of the methylation pattern of the hMSH2 promoter in colon cancer, using bisulfite genomic sequencing

The detailed methylation status of CpG sites in the promoter region of hMSH2 gene has yet not to be reported. We have mapped the complete methylation status of the hMSH2 promoter, a region that contains 75 CpG sites, using bisulfite genomic sequencing in 60 primary colorectal cancers. And the expres...

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Detalles Bibliográficos
Autores principales: Zhang, Hua, Fu, Wei-ling, Huang, Qing
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1570131/
https://www.ncbi.nlm.nih.gov/pubmed/16911791
http://dx.doi.org/10.1186/1477-3163-5-22
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author Zhang, Hua
Fu, Wei-ling
Huang, Qing
author_facet Zhang, Hua
Fu, Wei-ling
Huang, Qing
author_sort Zhang, Hua
collection PubMed
description The detailed methylation status of CpG sites in the promoter region of hMSH2 gene has yet not to be reported. We have mapped the complete methylation status of the hMSH2 promoter, a region that contains 75 CpG sites, using bisulfite genomic sequencing in 60 primary colorectal cancers. And the expression of hMSH2 was detected by immunohistochemistry. The hypermethylation of hMSH2 was detected in 18.33% (11/60) of tumor tissues. The protein of hMSH2 was detected in 41.67% (25/60) of tumor tissues. No hypermethylation of hMSH2 was detected in normal tissues. The protein of hMSH2 was detected in all normal tissues. Our study demonstrated that hMSH2 hypermethylation and protein expression were associated with the development of colorectal cancer.
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spelling pubmed-15701312006-09-19 Mapping of the methylation pattern of the hMSH2 promoter in colon cancer, using bisulfite genomic sequencing Zhang, Hua Fu, Wei-ling Huang, Qing J Carcinog Research The detailed methylation status of CpG sites in the promoter region of hMSH2 gene has yet not to be reported. We have mapped the complete methylation status of the hMSH2 promoter, a region that contains 75 CpG sites, using bisulfite genomic sequencing in 60 primary colorectal cancers. And the expression of hMSH2 was detected by immunohistochemistry. The hypermethylation of hMSH2 was detected in 18.33% (11/60) of tumor tissues. The protein of hMSH2 was detected in 41.67% (25/60) of tumor tissues. No hypermethylation of hMSH2 was detected in normal tissues. The protein of hMSH2 was detected in all normal tissues. Our study demonstrated that hMSH2 hypermethylation and protein expression were associated with the development of colorectal cancer. BioMed Central 2006-08-15 /pmc/articles/PMC1570131/ /pubmed/16911791 http://dx.doi.org/10.1186/1477-3163-5-22 Text en Copyright © 2006 Hua et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Zhang, Hua
Fu, Wei-ling
Huang, Qing
Mapping of the methylation pattern of the hMSH2 promoter in colon cancer, using bisulfite genomic sequencing
title Mapping of the methylation pattern of the hMSH2 promoter in colon cancer, using bisulfite genomic sequencing
title_full Mapping of the methylation pattern of the hMSH2 promoter in colon cancer, using bisulfite genomic sequencing
title_fullStr Mapping of the methylation pattern of the hMSH2 promoter in colon cancer, using bisulfite genomic sequencing
title_full_unstemmed Mapping of the methylation pattern of the hMSH2 promoter in colon cancer, using bisulfite genomic sequencing
title_short Mapping of the methylation pattern of the hMSH2 promoter in colon cancer, using bisulfite genomic sequencing
title_sort mapping of the methylation pattern of the hmsh2 promoter in colon cancer, using bisulfite genomic sequencing
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1570131/
https://www.ncbi.nlm.nih.gov/pubmed/16911791
http://dx.doi.org/10.1186/1477-3163-5-22
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