Cargando…
Detection of P24 protein in human breast cancer: influence of receptor status and oestrogen exposure.
The expression of oestrogen regulated protein, P24, was investigated in 69 breast cancers. At initial evaluation P24 protein was detected significantly more frequently and was present in significantly higher concentration in oestrogen receptor positive than in receptor negative tumours. There was, h...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1990
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971697/ https://www.ncbi.nlm.nih.gov/pubmed/2372491 |
_version_ | 1782134966190080000 |
---|---|
author | Seymour, L. Bezwoda, W. R. Meyer, K. Behr, C. |
author_facet | Seymour, L. Bezwoda, W. R. Meyer, K. Behr, C. |
author_sort | Seymour, L. |
collection | PubMed |
description | The expression of oestrogen regulated protein, P24, was investigated in 69 breast cancers. At initial evaluation P24 protein was detected significantly more frequently and was present in significantly higher concentration in oestrogen receptor positive than in receptor negative tumours. There was, however, no correlation between P24 staining and progesterone receptor, tumour ploidy or proliferative index. Nineteen patients received a short course of treatment with diethylstilboestrol. Following treatment with oestrogen, P24 staining became positive in 7/13 tumours previously negative for P24, including six tumours which were oestrogen receptor negative. Oestrogen administration also caused an increase of the proliferation index in 12/19 tumours, including 5/7 that were oestrogen receptor positive and 7/12 that were oestrogen receptor negative. In some instances oestrogenic stimulation of proliferation occurred together with increased P24 expression; in other instances proliferation index increased without induction of P24 synthesis. The in vivo effects of oestrogen in clinical breast cancer thus appear to show dissociation between enhancement of protein synthesis and cellular proliferation. |
format | Text |
id | pubmed-1971697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1990 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19716972009-09-10 Detection of P24 protein in human breast cancer: influence of receptor status and oestrogen exposure. Seymour, L. Bezwoda, W. R. Meyer, K. Behr, C. Br J Cancer Research Article The expression of oestrogen regulated protein, P24, was investigated in 69 breast cancers. At initial evaluation P24 protein was detected significantly more frequently and was present in significantly higher concentration in oestrogen receptor positive than in receptor negative tumours. There was, however, no correlation between P24 staining and progesterone receptor, tumour ploidy or proliferative index. Nineteen patients received a short course of treatment with diethylstilboestrol. Following treatment with oestrogen, P24 staining became positive in 7/13 tumours previously negative for P24, including six tumours which were oestrogen receptor negative. Oestrogen administration also caused an increase of the proliferation index in 12/19 tumours, including 5/7 that were oestrogen receptor positive and 7/12 that were oestrogen receptor negative. In some instances oestrogenic stimulation of proliferation occurred together with increased P24 expression; in other instances proliferation index increased without induction of P24 synthesis. The in vivo effects of oestrogen in clinical breast cancer thus appear to show dissociation between enhancement of protein synthesis and cellular proliferation. Nature Publishing Group 1990-06 /pmc/articles/PMC1971697/ /pubmed/2372491 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 Seymour, L. Bezwoda, W. R. Meyer, K. Behr, C. Detection of P24 protein in human breast cancer: influence of receptor status and oestrogen exposure. |
title | Detection of P24 protein in human breast cancer: influence of receptor status and oestrogen exposure. |
title_full | Detection of P24 protein in human breast cancer: influence of receptor status and oestrogen exposure. |
title_fullStr | Detection of P24 protein in human breast cancer: influence of receptor status and oestrogen exposure. |
title_full_unstemmed | Detection of P24 protein in human breast cancer: influence of receptor status and oestrogen exposure. |
title_short | Detection of P24 protein in human breast cancer: influence of receptor status and oestrogen exposure. |
title_sort | detection of p24 protein in human breast cancer: influence of receptor status and oestrogen exposure. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1971697/ https://www.ncbi.nlm.nih.gov/pubmed/2372491 |
work_keys_str_mv | AT seymourl detectionofp24proteininhumanbreastcancerinfluenceofreceptorstatusandoestrogenexposure AT bezwodawr detectionofp24proteininhumanbreastcancerinfluenceofreceptorstatusandoestrogenexposure AT meyerk detectionofp24proteininhumanbreastcancerinfluenceofreceptorstatusandoestrogenexposure AT behrc detectionofp24proteininhumanbreastcancerinfluenceofreceptorstatusandoestrogenexposure |