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Frequent loss of expression without sequence mutations of the DCC gene in primary gastric cancer
Loss of heterozygosity (LOH) on chromosome 18q21 is frequently found in various human cancers, suggesting the presence of tumour suppressor gene(s) in this chromosomal region. DCC is the most likely target of LOH because loss or reduction of DCC expression has been found in many types of cancers. Ho...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2001
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364029/ https://www.ncbi.nlm.nih.gov/pubmed/11461076 http://dx.doi.org/10.1054/bjoc.2001.1888 |
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author | Sato, K Tamura, G Tsuchiya, T Endoh, Y Usuba, O Kimura, W Motoyama, T |
author_facet | Sato, K Tamura, G Tsuchiya, T Endoh, Y Usuba, O Kimura, W Motoyama, T |
author_sort | Sato, K |
collection | PubMed |
description | Loss of heterozygosity (LOH) on chromosome 18q21 is frequently found in various human cancers, suggesting the presence of tumour suppressor gene(s) in this chromosomal region. DCC is the most likely target of LOH because loss or reduction of DCC expression has been found in many types of cancers. However, few reports have focused on sequence mutations of this gene. We investigated sequence mutations and expression of DCC in primary gastric cancers. We studied mutations in 25 of the 29 DCC exons by PCR-SSCP in 17 primary gastric cancers exhibiting LOH on 18q21. No mutations of DCC were found in any of the tumours, although 78% (47/60) of the primary tumours showed apparent loss or reduction of DCC expression by immunohistochemistry. Analysis of methylation status of DCC revealed that methylation frequently occurred in both primary tumours (75%; 45/60) and corresponding non-cancerous gastric mucosae (72%; 43/60). Methylated status of DCC was significantly correlated with the loss of DCC expression in primary tumours (P< 0.01). These results indicate that DCC is frequently silenced, probably by epigenetic mechanisms instead of sequence mutations in gastric cancer. © 2001 Cancer Research Campaign http://www.bjcancer.com |
format | Text |
id | pubmed-2364029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23640292009-09-10 Frequent loss of expression without sequence mutations of the DCC gene in primary gastric cancer Sato, K Tamura, G Tsuchiya, T Endoh, Y Usuba, O Kimura, W Motoyama, T Br J Cancer Regular Article Loss of heterozygosity (LOH) on chromosome 18q21 is frequently found in various human cancers, suggesting the presence of tumour suppressor gene(s) in this chromosomal region. DCC is the most likely target of LOH because loss or reduction of DCC expression has been found in many types of cancers. However, few reports have focused on sequence mutations of this gene. We investigated sequence mutations and expression of DCC in primary gastric cancers. We studied mutations in 25 of the 29 DCC exons by PCR-SSCP in 17 primary gastric cancers exhibiting LOH on 18q21. No mutations of DCC were found in any of the tumours, although 78% (47/60) of the primary tumours showed apparent loss or reduction of DCC expression by immunohistochemistry. Analysis of methylation status of DCC revealed that methylation frequently occurred in both primary tumours (75%; 45/60) and corresponding non-cancerous gastric mucosae (72%; 43/60). Methylated status of DCC was significantly correlated with the loss of DCC expression in primary tumours (P< 0.01). These results indicate that DCC is frequently silenced, probably by epigenetic mechanisms instead of sequence mutations in gastric cancer. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-07 /pmc/articles/PMC2364029/ /pubmed/11461076 http://dx.doi.org/10.1054/bjoc.2001.1888 Text en Copyright © 2001 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Regular Article Sato, K Tamura, G Tsuchiya, T Endoh, Y Usuba, O Kimura, W Motoyama, T Frequent loss of expression without sequence mutations of the DCC gene in primary gastric cancer |
title | Frequent loss of expression without sequence mutations of the DCC gene in primary gastric cancer |
title_full | Frequent loss of expression without sequence mutations of the DCC gene in primary gastric cancer |
title_fullStr | Frequent loss of expression without sequence mutations of the DCC gene in primary gastric cancer |
title_full_unstemmed | Frequent loss of expression without sequence mutations of the DCC gene in primary gastric cancer |
title_short | Frequent loss of expression without sequence mutations of the DCC gene in primary gastric cancer |
title_sort | frequent loss of expression without sequence mutations of the dcc gene in primary gastric cancer |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364029/ https://www.ncbi.nlm.nih.gov/pubmed/11461076 http://dx.doi.org/10.1054/bjoc.2001.1888 |
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