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The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system.

A total of 301 colorectal carcinoma (CRC) archival samples were analysed using the amplification-refractory mutation system (ARMS). Each sample was examined to determine the mutation status of codons 12 and 13 of the K-ras oncogene. The results from direct DNA sequence analysis carried out on 30 of...

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Autores principales: Fox, J. C., England, J., White, P., Ellison, G., Callaghan, K., Charlesworth, N. R., Hehir, J., McCarthy, T. L., Smith-Ravin, J., Talbot, I. C., Snary, D., Northover, J. M., Newton, C. R., Little, S.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150152/
https://www.ncbi.nlm.nih.gov/pubmed/9579832
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author Fox, J. C.
England, J.
White, P.
Ellison, G.
Callaghan, K.
Charlesworth, N. R.
Hehir, J.
McCarthy, T. L.
Smith-Ravin, J.
Talbot, I. C.
Snary, D.
Northover, J. M.
Newton, C. R.
Little, S.
author_facet Fox, J. C.
England, J.
White, P.
Ellison, G.
Callaghan, K.
Charlesworth, N. R.
Hehir, J.
McCarthy, T. L.
Smith-Ravin, J.
Talbot, I. C.
Snary, D.
Northover, J. M.
Newton, C. R.
Little, S.
author_sort Fox, J. C.
collection PubMed
description A total of 301 colorectal carcinoma (CRC) archival samples were analysed using the amplification-refractory mutation system (ARMS). Each sample was examined to determine the mutation status of codons 12 and 13 of the K-ras oncogene. The results from direct DNA sequence analysis carried out on 30 of the samples differed from the ARMS result in almost 50% of the cases as a result of the relative excess of wild-type to mutated DNA sequences. To assess the validity of the ARMS data, the polymerase chain reaction (PCR) was used to generate an amplicon from K-ras exon 1 from 23 of the samples. The PCR amplicons were cloned and sequenced, and the DNA sequence analysis of the cloned material was in agreement with the ARMS results in all but one case. This case represented a tumour that exhibited a five-nucleotide reversed inversion. The cloned sequence data confirm the sensitivity and specificity of the individual ARMS reactions and that it is possible in certain cases to detect additional, more complex, sequence variations. IMAGES:
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spelling pubmed-21501522009-09-10 The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system. Fox, J. C. England, J. White, P. Ellison, G. Callaghan, K. Charlesworth, N. R. Hehir, J. McCarthy, T. L. Smith-Ravin, J. Talbot, I. C. Snary, D. Northover, J. M. Newton, C. R. Little, S. Br J Cancer Research Article A total of 301 colorectal carcinoma (CRC) archival samples were analysed using the amplification-refractory mutation system (ARMS). Each sample was examined to determine the mutation status of codons 12 and 13 of the K-ras oncogene. The results from direct DNA sequence analysis carried out on 30 of the samples differed from the ARMS result in almost 50% of the cases as a result of the relative excess of wild-type to mutated DNA sequences. To assess the validity of the ARMS data, the polymerase chain reaction (PCR) was used to generate an amplicon from K-ras exon 1 from 23 of the samples. The PCR amplicons were cloned and sequenced, and the DNA sequence analysis of the cloned material was in agreement with the ARMS results in all but one case. This case represented a tumour that exhibited a five-nucleotide reversed inversion. The cloned sequence data confirm the sensitivity and specificity of the individual ARMS reactions and that it is possible in certain cases to detect additional, more complex, sequence variations. IMAGES: Nature Publishing Group 1998-04 /pmc/articles/PMC2150152/ /pubmed/9579832 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
Fox, J. C.
England, J.
White, P.
Ellison, G.
Callaghan, K.
Charlesworth, N. R.
Hehir, J.
McCarthy, T. L.
Smith-Ravin, J.
Talbot, I. C.
Snary, D.
Northover, J. M.
Newton, C. R.
Little, S.
The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system.
title The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system.
title_full The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system.
title_fullStr The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system.
title_full_unstemmed The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system.
title_short The detection of K-ras mutations in colorectal cancer using the amplification-refractory mutation system.
title_sort detection of k-ras mutations in colorectal cancer using the amplification-refractory mutation system.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2150152/
https://www.ncbi.nlm.nih.gov/pubmed/9579832
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