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Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma

Loss of heterozygosity (LOH) is frequent at the chromosomal region 11q22–q23 in several types of tumours of diverse cell origin. Previous investigations of LOH at this chromosomal region in colorectal carcinoma have been contradictory in their findings, and have only included between 1–4 loci. In or...

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Autores principales: Lee, A S-G, Seo, Y-C, Chang, A, Tohari, S, Eu, K-W, Seow-Choen, F, McGee, J O’D
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363538/
https://www.ncbi.nlm.nih.gov/pubmed/10952779
http://dx.doi.org/10.1054/bjoc.2000.1366
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author Lee, A S-G
Seo, Y-C
Chang, A
Tohari, S
Eu, K-W
Seow-Choen, F
McGee, J O’D
author_facet Lee, A S-G
Seo, Y-C
Chang, A
Tohari, S
Eu, K-W
Seow-Choen, F
McGee, J O’D
author_sort Lee, A S-G
collection PubMed
description Loss of heterozygosity (LOH) is frequent at the chromosomal region 11q22–q23 in several types of tumours of diverse cell origin. Previous investigations of LOH at this chromosomal region in colorectal carcinoma have been contradictory in their findings, and have only included between 1–4 loci. In order to define any regions of LOH on 11q23, we investigated 16 loci between D11S940 and D11S934 on the long arm of chromosome 11 using microsatellite analysis. Of 57 colorectal carcinomas specimens, 36 (63.2%) demonstrated LOH at one or more marker, with the highest frequencies of LOH at D11S1340 (41.0%), located between 105.13–111.97 Mb from the centromere, and D11S924 (37.1%) and D11S4107 (40.5%), both located approximately 113 Mb from the centromere. No statistically significant associations between LOH and age-of-presentation or Dukes’ stage were found. LOH was observed in colorectal tumours of all Dukes’ stages, including Dukes’ stages A and B, suggesting that the inactivation of a tumour suppressor gene(s) on 11q23 occurs in the early stages of colorectal carcinoma. These results confirm the presence of putative tumour suppressor gene(s) at chromosome 11q23, involved in the carcinogenesis of colorectal carcinoma, and will facilitate future identification of candidate genes. © 2000 Cancer Research Campaign
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spelling pubmed-23635382009-09-10 Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma Lee, A S-G Seo, Y-C Chang, A Tohari, S Eu, K-W Seow-Choen, F McGee, J O’D Br J Cancer Regular Article Loss of heterozygosity (LOH) is frequent at the chromosomal region 11q22–q23 in several types of tumours of diverse cell origin. Previous investigations of LOH at this chromosomal region in colorectal carcinoma have been contradictory in their findings, and have only included between 1–4 loci. In order to define any regions of LOH on 11q23, we investigated 16 loci between D11S940 and D11S934 on the long arm of chromosome 11 using microsatellite analysis. Of 57 colorectal carcinomas specimens, 36 (63.2%) demonstrated LOH at one or more marker, with the highest frequencies of LOH at D11S1340 (41.0%), located between 105.13–111.97 Mb from the centromere, and D11S924 (37.1%) and D11S4107 (40.5%), both located approximately 113 Mb from the centromere. No statistically significant associations between LOH and age-of-presentation or Dukes’ stage were found. LOH was observed in colorectal tumours of all Dukes’ stages, including Dukes’ stages A and B, suggesting that the inactivation of a tumour suppressor gene(s) on 11q23 occurs in the early stages of colorectal carcinoma. These results confirm the presence of putative tumour suppressor gene(s) at chromosome 11q23, involved in the carcinogenesis of colorectal carcinoma, and will facilitate future identification of candidate genes. © 2000 Cancer Research Campaign Nature Publishing Group 2000-09 2000-08-17 /pmc/articles/PMC2363538/ /pubmed/10952779 http://dx.doi.org/10.1054/bjoc.2000.1366 Text en Copyright © 2000 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
Lee, A S-G
Seo, Y-C
Chang, A
Tohari, S
Eu, K-W
Seow-Choen, F
McGee, J O’D
Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma
title Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma
title_full Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma
title_fullStr Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma
title_full_unstemmed Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma
title_short Detailed deletion mapping at chromosome 11q23 in colorectal carcinoma
title_sort detailed deletion mapping at chromosome 11q23 in colorectal carcinoma
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363538/
https://www.ncbi.nlm.nih.gov/pubmed/10952779
http://dx.doi.org/10.1054/bjoc.2000.1366
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