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PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival
BACKGROUND: PTTG1-interacting protein (PTTG1IP) is an oncogenic protein, which participates in metaphase-anaphase transition of the cell cycle through activation of securin (PTTG1). PTTG1IP promotes the shift of securin from the cell cytoplasm to the nucleus, allowing the interaction between separas...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658989/ https://www.ncbi.nlm.nih.gov/pubmed/29078751 http://dx.doi.org/10.1186/s12885-017-3694-6 |
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author | Repo, Heli Gurvits, Natalia Löyttyniemi, Eliisa Nykänen, Marjukka Lintunen, Minnamaija Karra, Henna Kurki, Samu Kuopio, Teijo Talvinen, Kati Söderström, Mirva Kronqvist, Pauliina |
author_facet | Repo, Heli Gurvits, Natalia Löyttyniemi, Eliisa Nykänen, Marjukka Lintunen, Minnamaija Karra, Henna Kurki, Samu Kuopio, Teijo Talvinen, Kati Söderström, Mirva Kronqvist, Pauliina |
author_sort | Repo, Heli |
collection | PubMed |
description | BACKGROUND: PTTG1-interacting protein (PTTG1IP) is an oncogenic protein, which participates in metaphase-anaphase transition of the cell cycle through activation of securin (PTTG1). PTTG1IP promotes the shift of securin from the cell cytoplasm to the nucleus, allowing the interaction between separase and securin. PTTG1IP overexpression has been previously observed in malignant disease, e.g. in breast carcinoma. However, the prognostic value of PTTG1IP in breast carcinoma patients has not previously been revealed. METHODS: A total of 497 breast carcinoma patients with up to 22-year follow-up were analysed for PTTG1IP and securin immunoexpression. The results were evaluated for correlations with the clinical prognosticators and patient survival. RESULTS: In our material, negative PTTG1IP immunoexpression predicted a 1.5-fold risk of breast cancer death (p = 0.02). However, adding securin immunoexpression to the analysis indicated an even stronger and independent prognostic power in the patient material (HR = 2.5, p < 0.0001). The subcellular location of securin was found with potential prognostic value also among the triple-negative breast carcinomas (n = 96, p = 0.052). CONCLUSIONS: PTTG1IP-negativity alone and in combination with high securin immunoexpression indicates a high risk of breast cancer death, resulting in up to 14-year survival difference in our material. |
format | Online Article Text |
id | pubmed-5658989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56589892017-11-01 PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival Repo, Heli Gurvits, Natalia Löyttyniemi, Eliisa Nykänen, Marjukka Lintunen, Minnamaija Karra, Henna Kurki, Samu Kuopio, Teijo Talvinen, Kati Söderström, Mirva Kronqvist, Pauliina BMC Cancer Research Article BACKGROUND: PTTG1-interacting protein (PTTG1IP) is an oncogenic protein, which participates in metaphase-anaphase transition of the cell cycle through activation of securin (PTTG1). PTTG1IP promotes the shift of securin from the cell cytoplasm to the nucleus, allowing the interaction between separase and securin. PTTG1IP overexpression has been previously observed in malignant disease, e.g. in breast carcinoma. However, the prognostic value of PTTG1IP in breast carcinoma patients has not previously been revealed. METHODS: A total of 497 breast carcinoma patients with up to 22-year follow-up were analysed for PTTG1IP and securin immunoexpression. The results were evaluated for correlations with the clinical prognosticators and patient survival. RESULTS: In our material, negative PTTG1IP immunoexpression predicted a 1.5-fold risk of breast cancer death (p = 0.02). However, adding securin immunoexpression to the analysis indicated an even stronger and independent prognostic power in the patient material (HR = 2.5, p < 0.0001). The subcellular location of securin was found with potential prognostic value also among the triple-negative breast carcinomas (n = 96, p = 0.052). CONCLUSIONS: PTTG1IP-negativity alone and in combination with high securin immunoexpression indicates a high risk of breast cancer death, resulting in up to 14-year survival difference in our material. BioMed Central 2017-10-27 /pmc/articles/PMC5658989/ /pubmed/29078751 http://dx.doi.org/10.1186/s12885-017-3694-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Repo, Heli Gurvits, Natalia Löyttyniemi, Eliisa Nykänen, Marjukka Lintunen, Minnamaija Karra, Henna Kurki, Samu Kuopio, Teijo Talvinen, Kati Söderström, Mirva Kronqvist, Pauliina PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival |
title | PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival |
title_full | PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival |
title_fullStr | PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival |
title_full_unstemmed | PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival |
title_short | PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival |
title_sort | pttg1-interacting protein (pttg1ip/pbf) predicts breast cancer survival |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658989/ https://www.ncbi.nlm.nih.gov/pubmed/29078751 http://dx.doi.org/10.1186/s12885-017-3694-6 |
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