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Nitric oxide synthase activity in human breast cancer.
Nitric oxide (NO) is generated by a family of isoenzymes (NO synthases) expressed in a wide range of mammalian cells. We have recently reported NO synthase expression in human gynaecological cancers. In this study we have assessed the activity and distribution of NO synthase in a series of human bre...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034139/ https://www.ncbi.nlm.nih.gov/pubmed/7541238 |
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author | Thomsen, L. L. Miles, D. W. Happerfield, L. Bobrow, L. G. Knowles, R. G. Moncada, S. |
author_facet | Thomsen, L. L. Miles, D. W. Happerfield, L. Bobrow, L. G. Knowles, R. G. Moncada, S. |
author_sort | Thomsen, L. L. |
collection | PubMed |
description | Nitric oxide (NO) is generated by a family of isoenzymes (NO synthases) expressed in a wide range of mammalian cells. We have recently reported NO synthase expression in human gynaecological cancers. In this study we have assessed the activity and distribution of NO synthase in a series of human breast tumours and in normal breast tissue. Calcium-dependent (constitutive) and -independent (inducible) NO synthase activity, as well as NO biosynthesis, was high in invasive tumours compared with benign or normal tissue. Furthermore, for invasive ductal carcinomas, NO biosynthesis was significantly greater for grade III compared with grade II tumours. Immunohistochemical investigations revealed immunolabelling with a monoclonal antibody to murine inducible NO synthase predominantly within tumour-associated macrophages. Immunolabelling with a polyclonal antiserum raised against rat brain NO synthase was also observed in vascular endothelial and myoepithelial cells. Thus NO synthase is expressed in human breast tumours, where its presence correlates with tumour grade. IMAGES: |
format | Text |
id | pubmed-2034139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20341392009-09-10 Nitric oxide synthase activity in human breast cancer. Thomsen, L. L. Miles, D. W. Happerfield, L. Bobrow, L. G. Knowles, R. G. Moncada, S. Br J Cancer Research Article Nitric oxide (NO) is generated by a family of isoenzymes (NO synthases) expressed in a wide range of mammalian cells. We have recently reported NO synthase expression in human gynaecological cancers. In this study we have assessed the activity and distribution of NO synthase in a series of human breast tumours and in normal breast tissue. Calcium-dependent (constitutive) and -independent (inducible) NO synthase activity, as well as NO biosynthesis, was high in invasive tumours compared with benign or normal tissue. Furthermore, for invasive ductal carcinomas, NO biosynthesis was significantly greater for grade III compared with grade II tumours. Immunohistochemical investigations revealed immunolabelling with a monoclonal antibody to murine inducible NO synthase predominantly within tumour-associated macrophages. Immunolabelling with a polyclonal antiserum raised against rat brain NO synthase was also observed in vascular endothelial and myoepithelial cells. Thus NO synthase is expressed in human breast tumours, where its presence correlates with tumour grade. IMAGES: Nature Publishing Group 1995-07 /pmc/articles/PMC2034139/ /pubmed/7541238 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 Thomsen, L. L. Miles, D. W. Happerfield, L. Bobrow, L. G. Knowles, R. G. Moncada, S. Nitric oxide synthase activity in human breast cancer. |
title | Nitric oxide synthase activity in human breast cancer. |
title_full | Nitric oxide synthase activity in human breast cancer. |
title_fullStr | Nitric oxide synthase activity in human breast cancer. |
title_full_unstemmed | Nitric oxide synthase activity in human breast cancer. |
title_short | Nitric oxide synthase activity in human breast cancer. |
title_sort | nitric oxide synthase activity in human breast cancer. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034139/ https://www.ncbi.nlm.nih.gov/pubmed/7541238 |
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