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Securin promotes the identification of favourable outcome in invasive breast cancer
BACKGROUND: Securin is a recently recognised oncogene with multiple known functions in initiation, progression and cell cycle regulation in several malignant diseases, including breast carcinoma. METHODS: In this paper, the prognostic value of securin is evaluated by immunohistochemistry in 310 pati...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743366/ https://www.ncbi.nlm.nih.gov/pubmed/19690544 http://dx.doi.org/10.1038/sj.bjc.6605237 |
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author | Talvinen, K Karra, H Hurme, S Nykänen, M Nieminen, A Anttinen, J Kuopio, T Kronqvist, P |
author_facet | Talvinen, K Karra, H Hurme, S Nykänen, M Nieminen, A Anttinen, J Kuopio, T Kronqvist, P |
author_sort | Talvinen, K |
collection | PubMed |
description | BACKGROUND: Securin is a recently recognised oncogene with multiple known functions in initiation, progression and cell cycle regulation in several malignant diseases, including breast carcinoma. METHODS: In this paper, the prognostic value of securin is evaluated by immunohistochemistry in 310 patients diagnosed with invasive breast cancer during a mammographic screening programme in Central Finland. All patients were directed to modern surgical and oncological treatments and were followed up for a maximum of 20 years. RESULTS: Our results suggest that securin immunopositivity is an independent prognosticator of invasive breast cancer. In our study, securin predicted breast cancer-specific survival among all cases of invasive breast cancer and subgroups divided according to histological type, Ki-67 proliferation status and tumour size. Especially in a multivariate analysis standardised for axillary lymph node status, patient's age and tumour size at the time of diagnosis, securin immunopositivity indicated a 13.1-fold risk of breast cancer death (P=0.024) among invasive ductal breast carcinomas with low Ki-67 positivity. CONCLUSION: Our present and previous results suggest that securin could be useful in clinical pathology to intensify the power of the established prognosticators of invasive breast cancer and, especially, to assist in identifying patients with a more favourable outcome than that indicated by Ki-67 alone. |
format | Text |
id | pubmed-2743366 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-27433662010-09-15 Securin promotes the identification of favourable outcome in invasive breast cancer Talvinen, K Karra, H Hurme, S Nykänen, M Nieminen, A Anttinen, J Kuopio, T Kronqvist, P Br J Cancer Molecular Diagnostics BACKGROUND: Securin is a recently recognised oncogene with multiple known functions in initiation, progression and cell cycle regulation in several malignant diseases, including breast carcinoma. METHODS: In this paper, the prognostic value of securin is evaluated by immunohistochemistry in 310 patients diagnosed with invasive breast cancer during a mammographic screening programme in Central Finland. All patients were directed to modern surgical and oncological treatments and were followed up for a maximum of 20 years. RESULTS: Our results suggest that securin immunopositivity is an independent prognosticator of invasive breast cancer. In our study, securin predicted breast cancer-specific survival among all cases of invasive breast cancer and subgroups divided according to histological type, Ki-67 proliferation status and tumour size. Especially in a multivariate analysis standardised for axillary lymph node status, patient's age and tumour size at the time of diagnosis, securin immunopositivity indicated a 13.1-fold risk of breast cancer death (P=0.024) among invasive ductal breast carcinomas with low Ki-67 positivity. CONCLUSION: Our present and previous results suggest that securin could be useful in clinical pathology to intensify the power of the established prognosticators of invasive breast cancer and, especially, to assist in identifying patients with a more favourable outcome than that indicated by Ki-67 alone. Nature Publishing Group 2009-09-15 2009-08-18 /pmc/articles/PMC2743366/ /pubmed/19690544 http://dx.doi.org/10.1038/sj.bjc.6605237 Text en Copyright © 2009 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 Talvinen, K Karra, H Hurme, S Nykänen, M Nieminen, A Anttinen, J Kuopio, T Kronqvist, P Securin promotes the identification of favourable outcome in invasive breast cancer |
title | Securin promotes the identification of favourable outcome in invasive breast cancer |
title_full | Securin promotes the identification of favourable outcome in invasive breast cancer |
title_fullStr | Securin promotes the identification of favourable outcome in invasive breast cancer |
title_full_unstemmed | Securin promotes the identification of favourable outcome in invasive breast cancer |
title_short | Securin promotes the identification of favourable outcome in invasive breast cancer |
title_sort | securin promotes the identification of favourable outcome in invasive breast cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743366/ https://www.ncbi.nlm.nih.gov/pubmed/19690544 http://dx.doi.org/10.1038/sj.bjc.6605237 |
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