Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Davies, Michael PA, O'Neill, Penny A, Innes, Helen, Sibson, D Ross
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
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
_version_ 1782123293032054784
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
work_keys_str_mv AT daviesmichaelpa hypersensitivek303roestrogenreceptoravariantnotfoundininvasivecarcinomas
AT oneillpennya hypersensitivek303roestrogenreceptoravariantnotfoundininvasivecarcinomas
AT inneshelen hypersensitivek303roestrogenreceptoravariantnotfoundininvasivecarcinomas
AT sibsondross hypersensitivek303roestrogenreceptoravariantnotfoundininvasivecarcinomas