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Expression and function of angiopoietin-1 in breast cancer
Angiopoietin-1 (Ang1) has been shown to act as an angiogenic promoter in embryonic angiogenesis by promoting vascular branching, pericyte recruitment and endothelial survival. We have investigated the role of Ang1 in tumour neovascularization under clinical conditions and in animal models. The expre...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2000
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363588/ https://www.ncbi.nlm.nih.gov/pubmed/11027428 http://dx.doi.org/10.1054/bjoc.2000.1437 |
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author | Hayes, A J Huang, W-Q Yu, J Maisonpierre, P C Liu, A Kern, F G Lippman, M E McLeskey, S W Li, L-Y |
author_facet | Hayes, A J Huang, W-Q Yu, J Maisonpierre, P C Liu, A Kern, F G Lippman, M E McLeskey, S W Li, L-Y |
author_sort | Hayes, A J |
collection | PubMed |
description | Angiopoietin-1 (Ang1) has been shown to act as an angiogenic promoter in embryonic angiogenesis by promoting vascular branching, pericyte recruitment and endothelial survival. We have investigated the role of Ang1 in tumour neovascularization under clinical conditions and in animal models. The expression of Ang1 in clinical breast cancer specimens was analysed by using laser-capture microdissection and reverse transcriptase-linked polymerase chain reaction (RT-PCR) on RNA isolated from the samples. Despite the expression of Ang1 in many human breast cancer cell lines, the gene was expressed in only three of 21 breast cancer clinical specimens, even though its receptor, Tie2, is abundant in the vasculature of all of these tumours. Ang1 was then overexpressed in a human breast cancer cell line (MCF-7) on its own and in conjunction with FGF1, an angiogenic factor shown to be able to increase the tumorigenicity of MCF-7 cells. High concentrations of Ang1 were produced in the conditioned media of the transfected cells (range 156–820 ng ml(–1)). However, in contrast to its physiological role as promoter of angiogenesis, overexpression of Ang1 did not enhance tumour growth, but instead caused up to a 3-fold retardation of tumour growth (P = 0.003). © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2363588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23635882009-09-10 Expression and function of angiopoietin-1 in breast cancer Hayes, A J Huang, W-Q Yu, J Maisonpierre, P C Liu, A Kern, F G Lippman, M E McLeskey, S W Li, L-Y Br J Cancer Regular Article Angiopoietin-1 (Ang1) has been shown to act as an angiogenic promoter in embryonic angiogenesis by promoting vascular branching, pericyte recruitment and endothelial survival. We have investigated the role of Ang1 in tumour neovascularization under clinical conditions and in animal models. The expression of Ang1 in clinical breast cancer specimens was analysed by using laser-capture microdissection and reverse transcriptase-linked polymerase chain reaction (RT-PCR) on RNA isolated from the samples. Despite the expression of Ang1 in many human breast cancer cell lines, the gene was expressed in only three of 21 breast cancer clinical specimens, even though its receptor, Tie2, is abundant in the vasculature of all of these tumours. Ang1 was then overexpressed in a human breast cancer cell line (MCF-7) on its own and in conjunction with FGF1, an angiogenic factor shown to be able to increase the tumorigenicity of MCF-7 cells. High concentrations of Ang1 were produced in the conditioned media of the transfected cells (range 156–820 ng ml(–1)). However, in contrast to its physiological role as promoter of angiogenesis, overexpression of Ang1 did not enhance tumour growth, but instead caused up to a 3-fold retardation of tumour growth (P = 0.003). © 2000 Cancer Research Campaign Nature Publishing Group 2000-11 /pmc/articles/PMC2363588/ /pubmed/11027428 http://dx.doi.org/10.1054/bjoc.2000.1437 Text en Copyright © 2000 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 Hayes, A J Huang, W-Q Yu, J Maisonpierre, P C Liu, A Kern, F G Lippman, M E McLeskey, S W Li, L-Y Expression and function of angiopoietin-1 in breast cancer |
title | Expression and function of angiopoietin-1 in breast cancer |
title_full | Expression and function of angiopoietin-1 in breast cancer |
title_fullStr | Expression and function of angiopoietin-1 in breast cancer |
title_full_unstemmed | Expression and function of angiopoietin-1 in breast cancer |
title_short | Expression and function of angiopoietin-1 in breast cancer |
title_sort | expression and function of angiopoietin-1 in breast cancer |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363588/ https://www.ncbi.nlm.nih.gov/pubmed/11027428 http://dx.doi.org/10.1054/bjoc.2000.1437 |
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