PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival
Repo, H., Gurvits, N., Löyttyniemi, E., Nykänen, M., Lintunen, M., Karra, H., Kurki, S., Kuopio, T., Talvinen, K., Söderström, M., & Kronqvist, P. (2017). PTTG1-interacting protein (PTTG1IP/PBF) predicts breast cancer survival. BMC Cancer, 17, Article 705. https://doi.org/10.1186/s12885-017-3694-6
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2017Copyright
© The Author(s). 2017 This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License.
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.
...
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Except where otherwise noted, this item's license is described as © The Author(s). 2017 This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License.
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