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A detailed analysis of the role of K-ras gene mutation in the progression of colorectal adenoma.
To elucidate the role of ras gene mutations during the early stage of colorectal tumour progression, K-ras gene mutations were analysed in 32 benign adenomas and 36 adenomas with focal carcinoma in the colorectum by microscraping of histologically pure regions from tissue sections, polymerase chain...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group|1
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063378/ https://www.ncbi.nlm.nih.gov/pubmed/9020477 |
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author | Ohnishi, T. Tomita, N. Monden, T. Ohue, M. Yana, I. Takami, K. Yamamoto, H. Yagyu, T. Kikkawa, N. Shimano, T. Monden, M. |
author_facet | Ohnishi, T. Tomita, N. Monden, T. Ohue, M. Yana, I. Takami, K. Yamamoto, H. Yagyu, T. Kikkawa, N. Shimano, T. Monden, M. |
author_sort | Ohnishi, T. |
collection | PubMed |
description | To elucidate the role of ras gene mutations during the early stage of colorectal tumour progression, K-ras gene mutations were analysed in 32 benign adenomas and 36 adenomas with focal carcinoma in the colorectum by microscraping of histologically pure regions from tissue sections, polymerase chain reaction-restriction fragment length polymorphism and in part by direct sequencing. Several regions were scraped out and analysed when an adenoma contained areas with different grades of dysplasia. The frequencies of K-ras gene mutation in mild dysplasia, moderate dysplasia and focal carcinoma were 19% (7/36), 51% (25/49) and 39% (14/36) respectively. The K-ras gene status was heterogeneous in 4 of the 11 benign adenomas from which multiple samples were obtained, and mutations were always found in the regions with more advanced dysplasia in these adenomas. Thirteen of the 36 adenomas with focal carcinoma showed heterogeneity of mutations between the adenoma region and the focal carcinoma. Seven of which had mutations only in the adenoma region. These findings indicated that the K-ras gene mutations occur during the late stage of adenoma progression and may confer a more advanced morphological phenotype of adenoma, but these mutations are not mainly involved in malignant transformation from adenoma to carcinoma. IMAGES: |
format | Text |
id | pubmed-2063378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Nature Publishing Group|1 |
record_format | MEDLINE/PubMed |
spelling | pubmed-20633782009-09-10 A detailed analysis of the role of K-ras gene mutation in the progression of colorectal adenoma. Ohnishi, T. Tomita, N. Monden, T. Ohue, M. Yana, I. Takami, K. Yamamoto, H. Yagyu, T. Kikkawa, N. Shimano, T. Monden, M. Br J Cancer Research Article To elucidate the role of ras gene mutations during the early stage of colorectal tumour progression, K-ras gene mutations were analysed in 32 benign adenomas and 36 adenomas with focal carcinoma in the colorectum by microscraping of histologically pure regions from tissue sections, polymerase chain reaction-restriction fragment length polymorphism and in part by direct sequencing. Several regions were scraped out and analysed when an adenoma contained areas with different grades of dysplasia. The frequencies of K-ras gene mutation in mild dysplasia, moderate dysplasia and focal carcinoma were 19% (7/36), 51% (25/49) and 39% (14/36) respectively. The K-ras gene status was heterogeneous in 4 of the 11 benign adenomas from which multiple samples were obtained, and mutations were always found in the regions with more advanced dysplasia in these adenomas. Thirteen of the 36 adenomas with focal carcinoma showed heterogeneity of mutations between the adenoma region and the focal carcinoma. Seven of which had mutations only in the adenoma region. These findings indicated that the K-ras gene mutations occur during the late stage of adenoma progression and may confer a more advanced morphological phenotype of adenoma, but these mutations are not mainly involved in malignant transformation from adenoma to carcinoma. IMAGES: Nature Publishing Group|1 1997 /pmc/articles/PMC2063378/ /pubmed/9020477 Text en 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 | Research Article Ohnishi, T. Tomita, N. Monden, T. Ohue, M. Yana, I. Takami, K. Yamamoto, H. Yagyu, T. Kikkawa, N. Shimano, T. Monden, M. A detailed analysis of the role of K-ras gene mutation in the progression of colorectal adenoma. |
title | A detailed analysis of the role of K-ras gene mutation in the progression of colorectal adenoma. |
title_full | A detailed analysis of the role of K-ras gene mutation in the progression of colorectal adenoma. |
title_fullStr | A detailed analysis of the role of K-ras gene mutation in the progression of colorectal adenoma. |
title_full_unstemmed | A detailed analysis of the role of K-ras gene mutation in the progression of colorectal adenoma. |
title_short | A detailed analysis of the role of K-ras gene mutation in the progression of colorectal adenoma. |
title_sort | detailed analysis of the role of k-ras gene mutation in the progression of colorectal adenoma. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063378/ https://www.ncbi.nlm.nih.gov/pubmed/9020477 |
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