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Significance of the metastasis-inducing protein AGR2 for outcome in hormonally treated breast cancer patients

The anterior gradient protein-2 (AGR2) is inducible by oestrogen and itself can induce metastasis in a rat model for breast cancer. Here, a rabbit antibody to recombinant human AGR2 was used to assess its prognostic significance in a retrospective cohort of 351 breast cancer patients treated by adju...

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Autores principales: Innes, H E, Liu, D, Barraclough, R, Davies, M P A, O'neill, P A, Platt-Higgins, A, de Silva Rudland, S, Sibson, D R, Rudland, P S
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361240/
https://www.ncbi.nlm.nih.gov/pubmed/16598187
http://dx.doi.org/10.1038/sj.bjc.6603065
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author Innes, H E
Liu, D
Barraclough, R
Davies, M P A
O'neill, P A
Platt-Higgins, A
de Silva Rudland, S
Sibson, D R
Rudland, P S
author_facet Innes, H E
Liu, D
Barraclough, R
Davies, M P A
O'neill, P A
Platt-Higgins, A
de Silva Rudland, S
Sibson, D R
Rudland, P S
author_sort Innes, H E
collection PubMed
description The anterior gradient protein-2 (AGR2) is inducible by oestrogen and itself can induce metastasis in a rat model for breast cancer. Here, a rabbit antibody to recombinant human AGR2 was used to assess its prognostic significance in a retrospective cohort of 351 breast cancer patients treated by adjuvant hormonal therapy. The antibody stains 66% of breast carcinomas to varying degrees. The percentage of positive carcinoma cells in tumours directly correlates with the level of AGR2 mRNA (Spearman's rank correlation, P=0.0007) and protein (linear regression analysis r(2)=0.95, P=0.0002). There is a significant association of staining of carcinomas for AGR2 with oestrogen receptor α (ERα) staining and with low histological grade (both Fisher's Exact test P<0.0001). In the ERα-positive cases, but not the ERα-negative cases, when subdivided into the separate staining classes for AGR2, there is a significantly progressive decrease in patient survival with increased staining (log rank test, P=0.006). The significant association of staining for AGR2 with patient death over a 10-year period (log rank test P=0.007, hazard ratio=3) only becomes significant at 6 years of follow-up. This may be due to the cessation of adjuvant hormonal therapy at an earlier time, resulting in adverse re-expression of the metastasis-inducing protein AGR2.
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spelling pubmed-23612402009-09-10 Significance of the metastasis-inducing protein AGR2 for outcome in hormonally treated breast cancer patients Innes, H E Liu, D Barraclough, R Davies, M P A O'neill, P A Platt-Higgins, A de Silva Rudland, S Sibson, D R Rudland, P S Br J Cancer Molecular Diagnostics The anterior gradient protein-2 (AGR2) is inducible by oestrogen and itself can induce metastasis in a rat model for breast cancer. Here, a rabbit antibody to recombinant human AGR2 was used to assess its prognostic significance in a retrospective cohort of 351 breast cancer patients treated by adjuvant hormonal therapy. The antibody stains 66% of breast carcinomas to varying degrees. The percentage of positive carcinoma cells in tumours directly correlates with the level of AGR2 mRNA (Spearman's rank correlation, P=0.0007) and protein (linear regression analysis r(2)=0.95, P=0.0002). There is a significant association of staining of carcinomas for AGR2 with oestrogen receptor α (ERα) staining and with low histological grade (both Fisher's Exact test P<0.0001). In the ERα-positive cases, but not the ERα-negative cases, when subdivided into the separate staining classes for AGR2, there is a significantly progressive decrease in patient survival with increased staining (log rank test, P=0.006). The significant association of staining for AGR2 with patient death over a 10-year period (log rank test P=0.007, hazard ratio=3) only becomes significant at 6 years of follow-up. This may be due to the cessation of adjuvant hormonal therapy at an earlier time, resulting in adverse re-expression of the metastasis-inducing protein AGR2. Nature Publishing Group 2006-04-10 2006-04-04 /pmc/articles/PMC2361240/ /pubmed/16598187 http://dx.doi.org/10.1038/sj.bjc.6603065 Text en Copyright © 2006 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 Molecular Diagnostics
Innes, H E
Liu, D
Barraclough, R
Davies, M P A
O'neill, P A
Platt-Higgins, A
de Silva Rudland, S
Sibson, D R
Rudland, P S
Significance of the metastasis-inducing protein AGR2 for outcome in hormonally treated breast cancer patients
title Significance of the metastasis-inducing protein AGR2 for outcome in hormonally treated breast cancer patients
title_full Significance of the metastasis-inducing protein AGR2 for outcome in hormonally treated breast cancer patients
title_fullStr Significance of the metastasis-inducing protein AGR2 for outcome in hormonally treated breast cancer patients
title_full_unstemmed Significance of the metastasis-inducing protein AGR2 for outcome in hormonally treated breast cancer patients
title_short Significance of the metastasis-inducing protein AGR2 for outcome in hormonally treated breast cancer patients
title_sort significance of the metastasis-inducing protein agr2 for outcome in hormonally treated breast cancer patients
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361240/
https://www.ncbi.nlm.nih.gov/pubmed/16598187
http://dx.doi.org/10.1038/sj.bjc.6603065
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