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Absence of progesterone receptor associated with secondary breast cancer in postmenopausal women

The relationship between expression of receptors for oestrogen and progesterone (ER and PR) and disease progression in breast cancer was investigated by comparing immunocytochemical determinations of ER and PR in fine needle aspirates from primary and secondary breast tumours. Rates of receptor expr...

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Autores principales: Balleine, R L, Earl, M J, Greenberg, M L, Clarke, C L
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362699/
https://www.ncbi.nlm.nih.gov/pubmed/10188907
http://dx.doi.org/10.1038/sj.bjc.6690249
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author Balleine, R L
Earl, M J
Greenberg, M L
Clarke, C L
author_facet Balleine, R L
Earl, M J
Greenberg, M L
Clarke, C L
author_sort Balleine, R L
collection PubMed
description The relationship between expression of receptors for oestrogen and progesterone (ER and PR) and disease progression in breast cancer was investigated by comparing immunocytochemical determinations of ER and PR in fine needle aspirates from primary and secondary breast tumours. Rates of receptor expression were significantly higher in primary than in secondary lesions: for ER 63.3% (n = 689) compared with 45.3% (n = 223), and for PR 53.7% (n = 443) compared with 33.1% (n = 121). The effect of menopausal status was examined by subdividing the patient cohort into those over or under the age of 50 years. In both instances, ER expression in secondary tumours was relatively low; however, only postmenopausal patients had significantly lower rates of PR expression in secondary tumours. Consistent with this, an increase in the ER+PR– profile in secondary tumours compared with primary cases from postmenopausal patients was seen, and in a multivariate analysis, a specific absence of PR expression in secondary tumours was revealed. Comparison of ER and PR expression in simultaneously sampled primary tumours and lymph node metastases from the same patient showed that receptor expression was stable with progression to a metastatic site as results were concordant for ER in 92% (n = 88) and PR in 93.8% of cases (n = 65). These results suggest that absence of PR expression in primary breast cancer is associated with disease progression and may be a marker of an aggressive tumour phenotype. © 1999 Cancer Research Campaign
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spelling pubmed-23626992009-09-10 Absence of progesterone receptor associated with secondary breast cancer in postmenopausal women Balleine, R L Earl, M J Greenberg, M L Clarke, C L Br J Cancer Regular Article The relationship between expression of receptors for oestrogen and progesterone (ER and PR) and disease progression in breast cancer was investigated by comparing immunocytochemical determinations of ER and PR in fine needle aspirates from primary and secondary breast tumours. Rates of receptor expression were significantly higher in primary than in secondary lesions: for ER 63.3% (n = 689) compared with 45.3% (n = 223), and for PR 53.7% (n = 443) compared with 33.1% (n = 121). The effect of menopausal status was examined by subdividing the patient cohort into those over or under the age of 50 years. In both instances, ER expression in secondary tumours was relatively low; however, only postmenopausal patients had significantly lower rates of PR expression in secondary tumours. Consistent with this, an increase in the ER+PR– profile in secondary tumours compared with primary cases from postmenopausal patients was seen, and in a multivariate analysis, a specific absence of PR expression in secondary tumours was revealed. Comparison of ER and PR expression in simultaneously sampled primary tumours and lymph node metastases from the same patient showed that receptor expression was stable with progression to a metastatic site as results were concordant for ER in 92% (n = 88) and PR in 93.8% of cases (n = 65). These results suggest that absence of PR expression in primary breast cancer is associated with disease progression and may be a marker of an aggressive tumour phenotype. © 1999 Cancer Research Campaign Nature Publishing Group 1999-03 /pmc/articles/PMC2362699/ /pubmed/10188907 http://dx.doi.org/10.1038/sj.bjc.6690249 Text en Copyright © 1999 Cancer Research Campaign 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 Regular Article
Balleine, R L
Earl, M J
Greenberg, M L
Clarke, C L
Absence of progesterone receptor associated with secondary breast cancer in postmenopausal women
title Absence of progesterone receptor associated with secondary breast cancer in postmenopausal women
title_full Absence of progesterone receptor associated with secondary breast cancer in postmenopausal women
title_fullStr Absence of progesterone receptor associated with secondary breast cancer in postmenopausal women
title_full_unstemmed Absence of progesterone receptor associated with secondary breast cancer in postmenopausal women
title_short Absence of progesterone receptor associated with secondary breast cancer in postmenopausal women
title_sort absence of progesterone receptor associated with secondary breast cancer in postmenopausal women
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362699/
https://www.ncbi.nlm.nih.gov/pubmed/10188907
http://dx.doi.org/10.1038/sj.bjc.6690249
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