Cargando…
Epidermal and transforming growth factor alpha in patients with breast tumours.
Measurements of transforming growth factor alpha (TGF-alpha) in cancer patients have produced variable results. We have now used a specific radioimmunoassay (RIA) and a mitogenic assay to evaluate TGF-alpha content of tumour and urine samples separated by an analytical HPLC system. Urine samples fro...
Autores principales: | , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1989
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2247132/ https://www.ncbi.nlm.nih.gov/pubmed/2785399 |
_version_ | 1782150916380557312 |
---|---|
author | Gregory, H. Thomas, C. E. Willshire, I. R. Young, J. A. Anderson, H. Baildam, A. Howell, A. |
author_facet | Gregory, H. Thomas, C. E. Willshire, I. R. Young, J. A. Anderson, H. Baildam, A. Howell, A. |
author_sort | Gregory, H. |
collection | PubMed |
description | Measurements of transforming growth factor alpha (TGF-alpha) in cancer patients have produced variable results. We have now used a specific radioimmunoassay (RIA) and a mitogenic assay to evaluate TGF-alpha content of tumour and urine samples separated by an analytical HPLC system. Urine samples from patients with breast tumours and from age matched controls gave TGF-alpha amounts ranging from 0 to 61.5 ng 24 h-1 compared to urogastrone epidermal growth factor figures of 3.0-26.2 micrograms 24 h-1. The quantities of TGF-alpha in patient and control groups were not significantly different. The majority of breast tumour extracts contained mitogenic material eluting from the HPLC system at the TGF-alpha calibration point. Measurement by RIA of combined samples from each group showed that steroid receptor positive tumours had a mean figure of 14.8 ng g-1 tissue and steroid receptor negative 7.4 ng g-1. Receptor positive tumours from patients treated with an antioestrogen, tamoxifen citrate (Nolvadex), had 0.16 ng g-1. Thus TGF-alpha is found in tumours as a biologically active entity and in quantities sufficient to promote cell division. In addition the observation that tamoxifen causes a significant reduction in the content of TGF-alpha may be an additional beneficial action. |
format | Text |
id | pubmed-2247132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22471322009-09-10 Epidermal and transforming growth factor alpha in patients with breast tumours. Gregory, H. Thomas, C. E. Willshire, I. R. Young, J. A. Anderson, H. Baildam, A. Howell, A. Br J Cancer Research Article Measurements of transforming growth factor alpha (TGF-alpha) in cancer patients have produced variable results. We have now used a specific radioimmunoassay (RIA) and a mitogenic assay to evaluate TGF-alpha content of tumour and urine samples separated by an analytical HPLC system. Urine samples from patients with breast tumours and from age matched controls gave TGF-alpha amounts ranging from 0 to 61.5 ng 24 h-1 compared to urogastrone epidermal growth factor figures of 3.0-26.2 micrograms 24 h-1. The quantities of TGF-alpha in patient and control groups were not significantly different. The majority of breast tumour extracts contained mitogenic material eluting from the HPLC system at the TGF-alpha calibration point. Measurement by RIA of combined samples from each group showed that steroid receptor positive tumours had a mean figure of 14.8 ng g-1 tissue and steroid receptor negative 7.4 ng g-1. Receptor positive tumours from patients treated with an antioestrogen, tamoxifen citrate (Nolvadex), had 0.16 ng g-1. Thus TGF-alpha is found in tumours as a biologically active entity and in quantities sufficient to promote cell division. In addition the observation that tamoxifen causes a significant reduction in the content of TGF-alpha may be an additional beneficial action. Nature Publishing Group 1989-04 /pmc/articles/PMC2247132/ /pubmed/2785399 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 Gregory, H. Thomas, C. E. Willshire, I. R. Young, J. A. Anderson, H. Baildam, A. Howell, A. Epidermal and transforming growth factor alpha in patients with breast tumours. |
title | Epidermal and transforming growth factor alpha in patients with breast tumours. |
title_full | Epidermal and transforming growth factor alpha in patients with breast tumours. |
title_fullStr | Epidermal and transforming growth factor alpha in patients with breast tumours. |
title_full_unstemmed | Epidermal and transforming growth factor alpha in patients with breast tumours. |
title_short | Epidermal and transforming growth factor alpha in patients with breast tumours. |
title_sort | epidermal and transforming growth factor alpha in patients with breast tumours. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2247132/ https://www.ncbi.nlm.nih.gov/pubmed/2785399 |
work_keys_str_mv | AT gregoryh epidermalandtransforminggrowthfactoralphainpatientswithbreasttumours AT thomasce epidermalandtransforminggrowthfactoralphainpatientswithbreasttumours AT willshireir epidermalandtransforminggrowthfactoralphainpatientswithbreasttumours AT youngja epidermalandtransforminggrowthfactoralphainpatientswithbreasttumours AT andersonh epidermalandtransforminggrowthfactoralphainpatientswithbreasttumours AT baildama epidermalandtransforminggrowthfactoralphainpatientswithbreasttumours AT howella epidermalandtransforminggrowthfactoralphainpatientswithbreasttumours |