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Metallothionein expression in human breast cancer.
Metallothioneins are ubiquitous low molecular weight proteins characterised by high cysteine content and affinity for binding heavy metals. Abnormal metallothionein function and expression have been implicated in various disease states, including neoplasia. The aim of this study was to investigate m...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1995
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034037/ https://www.ncbi.nlm.nih.gov/pubmed/7547250 |
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author | Goulding, H. Jasani, B. Pereira, H. Reid, A. Galea, M. Bell, J. A. Elston, C. W. Robertson, J. F. Blamey, R. W. Nicholson, R. A. |
author_facet | Goulding, H. Jasani, B. Pereira, H. Reid, A. Galea, M. Bell, J. A. Elston, C. W. Robertson, J. F. Blamey, R. W. Nicholson, R. A. |
author_sort | Goulding, H. |
collection | PubMed |
description | Metallothioneins are ubiquitous low molecular weight proteins characterised by high cysteine content and affinity for binding heavy metals. Abnormal metallothionein function and expression have been implicated in various disease states, including neoplasia. The aim of this study was to investigate metallothionein expression in human breast carcinoma. Sections of routinely fixed and processed blocks of tumour from 100 consecutive cases of primary operable breast carcinoma were stained for metallothionein using a recently developed monoclonal antibody and a standard immunohistochemical technique. Expression was scored on the basis of microscopical assessment of percentage of tumour cells staining. One patient was lost to follow-up and excluded from the study. A significant association (P < 0.0001) was observed between metallothionein expression and tumour type, with low levels being observed in tumours of good prognostic type. There was also a significant association with local recurrence (P < 0.02) and a significant difference (P < 0.02) in both survival and disease-free interval between tumours showing low and high levels of expression, the latter indicating a poor prognosis. No relationship was observed with patient age, tumour size, lymph node stage, histological grade, vascular invasion, menopausal status or oestrogen receptor status. The assessment of metallothionein expression in human breast cancer appears to provide prognostic information and may have important implications for understanding its development. IMAGES: |
format | Text |
id | pubmed-2034037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20340372009-09-10 Metallothionein expression in human breast cancer. Goulding, H. Jasani, B. Pereira, H. Reid, A. Galea, M. Bell, J. A. Elston, C. W. Robertson, J. F. Blamey, R. W. Nicholson, R. A. Br J Cancer Research Article Metallothioneins are ubiquitous low molecular weight proteins characterised by high cysteine content and affinity for binding heavy metals. Abnormal metallothionein function and expression have been implicated in various disease states, including neoplasia. The aim of this study was to investigate metallothionein expression in human breast carcinoma. Sections of routinely fixed and processed blocks of tumour from 100 consecutive cases of primary operable breast carcinoma were stained for metallothionein using a recently developed monoclonal antibody and a standard immunohistochemical technique. Expression was scored on the basis of microscopical assessment of percentage of tumour cells staining. One patient was lost to follow-up and excluded from the study. A significant association (P < 0.0001) was observed between metallothionein expression and tumour type, with low levels being observed in tumours of good prognostic type. There was also a significant association with local recurrence (P < 0.02) and a significant difference (P < 0.02) in both survival and disease-free interval between tumours showing low and high levels of expression, the latter indicating a poor prognosis. No relationship was observed with patient age, tumour size, lymph node stage, histological grade, vascular invasion, menopausal status or oestrogen receptor status. The assessment of metallothionein expression in human breast cancer appears to provide prognostic information and may have important implications for understanding its development. IMAGES: Nature Publishing Group 1995-10 /pmc/articles/PMC2034037/ /pubmed/7547250 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 Goulding, H. Jasani, B. Pereira, H. Reid, A. Galea, M. Bell, J. A. Elston, C. W. Robertson, J. F. Blamey, R. W. Nicholson, R. A. Metallothionein expression in human breast cancer. |
title | Metallothionein expression in human breast cancer. |
title_full | Metallothionein expression in human breast cancer. |
title_fullStr | Metallothionein expression in human breast cancer. |
title_full_unstemmed | Metallothionein expression in human breast cancer. |
title_short | Metallothionein expression in human breast cancer. |
title_sort | metallothionein expression in human breast cancer. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034037/ https://www.ncbi.nlm.nih.gov/pubmed/7547250 |
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