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Hypersensitive K303R oestrogen receptor-α variant not found in invasive carcinomas
INTRODUCTION: Genetic abnormalities or mutations in premalignant breast lesions may have a role in progression toward malignancy or influence the behaviour of subsequent disease. The A908G (Lys303→Arg) change in the gene encoding oestrogen receptor-α (ER-α) creates a hypersensitivity to oestradiol a...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1064111/ https://www.ncbi.nlm.nih.gov/pubmed/15642159 http://dx.doi.org/10.1186/bcr965 |
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author | Davies, Michael PA O'Neill, Penny A Innes, Helen Sibson, D Ross |
author_facet | Davies, Michael PA O'Neill, Penny A Innes, Helen Sibson, D Ross |
author_sort | Davies, Michael PA |
collection | PubMed |
description | INTRODUCTION: Genetic abnormalities or mutations in premalignant breast lesions may have a role in progression toward malignancy or influence the behaviour of subsequent disease. The A908G (Lys303→Arg) change in the gene encoding oestrogen receptor-α (ER-α) creates a hypersensitivity to oestradiol and would have significant consequences if present in breast carcinoma, especially those treated with endocrine therapy. We have therefore examined a panel of endocrine-treated invasive carcinomas for the presence of this mutation. METHODS: Sequencing of control DNA was shown to detect mutation present in as little as 15% of the starting material. Enrichment for the mutation by using MboII restriction digestion allowed the detection of mutant present at 1% or less. We applied these techniques to genomic DNA and cDNA from 136 invasive breast carcinomas. RESULTS: No evidence of the A908G mutation was found with either technique. The incidence of this mutation in our panel of tumours is therefore significantly less than previously reported. CONCLUSION: The fact that the mutation was not found leads us to believe that this mutation is absent from most cells in invasive carcinomas and furthermore that the major expression product of the ER-α gene in cancers does not contain the K303R mutation. It is therefore unlikely to influence the effectiveness of endocrine treatment. |
format | Text |
id | pubmed-1064111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-10641112005-03-11 Hypersensitive K303R oestrogen receptor-α variant not found in invasive carcinomas Davies, Michael PA O'Neill, Penny A Innes, Helen Sibson, D Ross Breast Cancer Res Research Article INTRODUCTION: Genetic abnormalities or mutations in premalignant breast lesions may have a role in progression toward malignancy or influence the behaviour of subsequent disease. The A908G (Lys303→Arg) change in the gene encoding oestrogen receptor-α (ER-α) creates a hypersensitivity to oestradiol and would have significant consequences if present in breast carcinoma, especially those treated with endocrine therapy. We have therefore examined a panel of endocrine-treated invasive carcinomas for the presence of this mutation. METHODS: Sequencing of control DNA was shown to detect mutation present in as little as 15% of the starting material. Enrichment for the mutation by using MboII restriction digestion allowed the detection of mutant present at 1% or less. We applied these techniques to genomic DNA and cDNA from 136 invasive breast carcinomas. RESULTS: No evidence of the A908G mutation was found with either technique. The incidence of this mutation in our panel of tumours is therefore significantly less than previously reported. CONCLUSION: The fact that the mutation was not found leads us to believe that this mutation is absent from most cells in invasive carcinomas and furthermore that the major expression product of the ER-α gene in cancers does not contain the K303R mutation. It is therefore unlikely to influence the effectiveness of endocrine treatment. BioMed Central 2005 2004-11-23 /pmc/articles/PMC1064111/ /pubmed/15642159 http://dx.doi.org/10.1186/bcr965 Text en Copyright © 2004 Davies et al.; licensee BioMed Central Ltd. |
spellingShingle | Research Article Davies, Michael PA O'Neill, Penny A Innes, Helen Sibson, D Ross Hypersensitive K303R oestrogen receptor-α variant not found in invasive carcinomas |
title | Hypersensitive K303R oestrogen receptor-α variant not found in invasive carcinomas |
title_full | Hypersensitive K303R oestrogen receptor-α variant not found in invasive carcinomas |
title_fullStr | Hypersensitive K303R oestrogen receptor-α variant not found in invasive carcinomas |
title_full_unstemmed | Hypersensitive K303R oestrogen receptor-α variant not found in invasive carcinomas |
title_short | Hypersensitive K303R oestrogen receptor-α variant not found in invasive carcinomas |
title_sort | hypersensitive k303r oestrogen receptor-α variant not found in invasive carcinomas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1064111/ https://www.ncbi.nlm.nih.gov/pubmed/15642159 http://dx.doi.org/10.1186/bcr965 |
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