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Oestrogen receptor β and neoadjuvant therapy with tamoxifen: prediction of response and effects of treatment
In order to elucidate the relative importance of oestrogen receptor (ER)α, ERβ and an ERβ variant (ERβ2/βcx) in the response of breast cancers to tamoxifen, tumour levels of each receptor were assessed in 36 patients before and after 3 months of neoadjuvant treatment with tamoxifen (20 mg daily). Al...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361404/ https://www.ncbi.nlm.nih.gov/pubmed/16622466 http://dx.doi.org/10.1038/sj.bjc.6603082 |
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author | Miller, W R Anderson, T J Dixon, J M Saunders, P T K |
author_facet | Miller, W R Anderson, T J Dixon, J M Saunders, P T K |
author_sort | Miller, W R |
collection | PubMed |
description | In order to elucidate the relative importance of oestrogen receptor (ER)α, ERβ and an ERβ variant (ERβ2/βcx) in the response of breast cancers to tamoxifen, tumour levels of each receptor were assessed in 36 patients before and after 3 months of neoadjuvant treatment with tamoxifen (20 mg daily). All patients were postmenopausal women presenting with large ERα-positive breast cancers. Clinical response to treatment was assessed by tumour volume changes as determined from sequential ultrasounds and pathological response by comparison of the tumour morphology before and after treatment. Of 33 cases, 23 (70%) were classified as having a clinical response and 16 (48%) as having a response pathologically. All tumours stained positively for ERα and ERβ and 15 out of 33 (45%) for ERβ2/βcx. There were no significant differences in quantitative expression of any receptor between tumours that subsequently responded and that did not, whether response was assessed clinically or pathologically. Tamoxifen treatment was associated with a decrease in ERα, but an increase was the most frequent change (17 out of 33) in ERβ, and no consistent change was evident in staining of the ERβ2/βcx variant. In summary, ERβ1 and ERβ2/βcx variant protein are detected in ERα-positive breast tumours but their expression is not associated with a response to tamoxifen. Differential changes in ERα and ERβ were seen with treatment. |
format | Text |
id | pubmed-2361404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23614042009-09-10 Oestrogen receptor β and neoadjuvant therapy with tamoxifen: prediction of response and effects of treatment Miller, W R Anderson, T J Dixon, J M Saunders, P T K Br J Cancer Molecular Diagnostics In order to elucidate the relative importance of oestrogen receptor (ER)α, ERβ and an ERβ variant (ERβ2/βcx) in the response of breast cancers to tamoxifen, tumour levels of each receptor were assessed in 36 patients before and after 3 months of neoadjuvant treatment with tamoxifen (20 mg daily). All patients were postmenopausal women presenting with large ERα-positive breast cancers. Clinical response to treatment was assessed by tumour volume changes as determined from sequential ultrasounds and pathological response by comparison of the tumour morphology before and after treatment. Of 33 cases, 23 (70%) were classified as having a clinical response and 16 (48%) as having a response pathologically. All tumours stained positively for ERα and ERβ and 15 out of 33 (45%) for ERβ2/βcx. There were no significant differences in quantitative expression of any receptor between tumours that subsequently responded and that did not, whether response was assessed clinically or pathologically. Tamoxifen treatment was associated with a decrease in ERα, but an increase was the most frequent change (17 out of 33) in ERβ, and no consistent change was evident in staining of the ERβ2/βcx variant. In summary, ERβ1 and ERβ2/βcx variant protein are detected in ERα-positive breast tumours but their expression is not associated with a response to tamoxifen. Differential changes in ERα and ERβ were seen with treatment. Nature Publishing Group 2006-05-08 2006-04-18 /pmc/articles/PMC2361404/ /pubmed/16622466 http://dx.doi.org/10.1038/sj.bjc.6603082 Text en Copyright © 2006 Cancer Research UK 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 | Molecular Diagnostics Miller, W R Anderson, T J Dixon, J M Saunders, P T K Oestrogen receptor β and neoadjuvant therapy with tamoxifen: prediction of response and effects of treatment |
title | Oestrogen receptor β and neoadjuvant therapy with tamoxifen: prediction of response and effects of treatment |
title_full | Oestrogen receptor β and neoadjuvant therapy with tamoxifen: prediction of response and effects of treatment |
title_fullStr | Oestrogen receptor β and neoadjuvant therapy with tamoxifen: prediction of response and effects of treatment |
title_full_unstemmed | Oestrogen receptor β and neoadjuvant therapy with tamoxifen: prediction of response and effects of treatment |
title_short | Oestrogen receptor β and neoadjuvant therapy with tamoxifen: prediction of response and effects of treatment |
title_sort | oestrogen receptor β and neoadjuvant therapy with tamoxifen: prediction of response and effects of treatment |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361404/ https://www.ncbi.nlm.nih.gov/pubmed/16622466 http://dx.doi.org/10.1038/sj.bjc.6603082 |
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