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Growth arrest-specific gene 6 expression in human breast cancer
Growth arrest-specific gene 6 (Gas6), identified in 1995, acts as the ligand to the Axl/Tyro3 family of tyrosine kinase receptors and exerts mitogenic activity when bound to these receptors. Overexpression of the Axl/Tyro3 receptor family has been found in breast, ovarian and lung tumours. Gas6 is u...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275480/ https://www.ncbi.nlm.nih.gov/pubmed/18283315 http://dx.doi.org/10.1038/sj.bjc.6604260 |
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author | Mc Cormack, O Chung, W Y Fitzpatrick, P Cooke, F Flynn, B Harrison, M Fox, E Gallagher, E Goldrick, A Mc Dervan, P A Mc Cann, A Kerin, M J |
author_facet | Mc Cormack, O Chung, W Y Fitzpatrick, P Cooke, F Flynn, B Harrison, M Fox, E Gallagher, E Goldrick, A Mc Dervan, P A Mc Cann, A Kerin, M J |
author_sort | Mc Cormack, O |
collection | PubMed |
description | Growth arrest-specific gene 6 (Gas6), identified in 1995, acts as the ligand to the Axl/Tyro3 family of tyrosine kinase receptors and exerts mitogenic activity when bound to these receptors. Overexpression of the Axl/Tyro3 receptor family has been found in breast, ovarian and lung tumours. Gas6 is upregulated 23-fold by progesterone acting through the progesterone receptor B (PRB). Recently, Gas6 has been shown to be a target for overexpression and amplification in breast cancer. Quantitative real-time PCR analysis was used to determine the levels of Gas6 mRNA expression in 49 primary breast carcinomas. Expression of PRB protein was evaluated immunohistochemically with a commercially available PRB antibody. The results showed a positive association between PRB protein and Gas6 mRNA levels (P=0.04). Gas6 correlated positively with a number of favourable prognostic variables including lymph node negativity (P=0.0002), younger age at diagnosis (P=0.04), smaller size of tumours (P=0.02), low Nottingham prognostic index scores (P=0.03) and low nuclear morphology (P=0.03). This study verifies for the first time the association between PRB and Gas6 in breast cancer tissue. |
format | Text |
id | pubmed-2275480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22754802009-09-10 Growth arrest-specific gene 6 expression in human breast cancer Mc Cormack, O Chung, W Y Fitzpatrick, P Cooke, F Flynn, B Harrison, M Fox, E Gallagher, E Goldrick, A Mc Dervan, P A Mc Cann, A Kerin, M J Br J Cancer Genetics and Genomics Growth arrest-specific gene 6 (Gas6), identified in 1995, acts as the ligand to the Axl/Tyro3 family of tyrosine kinase receptors and exerts mitogenic activity when bound to these receptors. Overexpression of the Axl/Tyro3 receptor family has been found in breast, ovarian and lung tumours. Gas6 is upregulated 23-fold by progesterone acting through the progesterone receptor B (PRB). Recently, Gas6 has been shown to be a target for overexpression and amplification in breast cancer. Quantitative real-time PCR analysis was used to determine the levels of Gas6 mRNA expression in 49 primary breast carcinomas. Expression of PRB protein was evaluated immunohistochemically with a commercially available PRB antibody. The results showed a positive association between PRB protein and Gas6 mRNA levels (P=0.04). Gas6 correlated positively with a number of favourable prognostic variables including lymph node negativity (P=0.0002), younger age at diagnosis (P=0.04), smaller size of tumours (P=0.02), low Nottingham prognostic index scores (P=0.03) and low nuclear morphology (P=0.03). This study verifies for the first time the association between PRB and Gas6 in breast cancer tissue. Nature Publishing Group 2008-03-25 2008-02-19 /pmc/articles/PMC2275480/ /pubmed/18283315 http://dx.doi.org/10.1038/sj.bjc.6604260 Text en Copyright © 2008 Cancer Research UK 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 | Genetics and Genomics Mc Cormack, O Chung, W Y Fitzpatrick, P Cooke, F Flynn, B Harrison, M Fox, E Gallagher, E Goldrick, A Mc Dervan, P A Mc Cann, A Kerin, M J Growth arrest-specific gene 6 expression in human breast cancer |
title | Growth arrest-specific gene 6 expression in human breast cancer |
title_full | Growth arrest-specific gene 6 expression in human breast cancer |
title_fullStr | Growth arrest-specific gene 6 expression in human breast cancer |
title_full_unstemmed | Growth arrest-specific gene 6 expression in human breast cancer |
title_short | Growth arrest-specific gene 6 expression in human breast cancer |
title_sort | growth arrest-specific gene 6 expression in human breast cancer |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2275480/ https://www.ncbi.nlm.nih.gov/pubmed/18283315 http://dx.doi.org/10.1038/sj.bjc.6604260 |
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