Islam M. Miligy
Thioredoxin-interacting protein is an independent risk stratifier for breast ductal carcinoma in situ
Miligy, Islam M.; Gorringe, Kylie L.; Toss, Michael S.; Al-Kawaz, Abdubaqi; Simpson, Peter; Diez-Rodriguez, Maria; Nolan, Christopher C.; Ellis, Ian O.; Green, Andrew R.; Rakha, Emad
Authors
Kylie L. Gorringe
Michael S. Toss
Abdubaqi Al-Kawaz
Peter Simpson
Maria Diez-Rodriguez
Christopher C. Nolan
Professor IAN ELLIS IAN.ELLIS@NOTTINGHAM.AC.UK
Professor of Cancer Pathology
ANDREW GREEN andrew.green@nottingham.ac.uk
Associate Professor
EMAD RAKHA Emad.Rakha@nottingham.ac.uk
Professor of Breast Cancer Pathology
Abstract
Current clinicopathological parameters are useful predictors of breast ductal carcinoma in situ behaviour, but they are insufficient to define high risk patients for disease progression precisely. Thioredoxin interacting protein (TXNIP) is a key player of oxidative stress. This study aims to evaluate the role of TXNIP as a predictor of ductal carcinoma in situ progression. Tissue microarrays from 776 pure ductal carcinoma in situ and 239 mixed ductal carcinoma in situ and invasive tumors were constructed. All patients were treated at a single institution with a long-term follow-up and TXNIP expression was assessed using immunohistochemistry. TXNIP expression was investigated in terms of associations with clinicopathological and molecular features and patient outcome. Loss/reduced cytoplasmic expression of TXNIP was associated with features of aggressiveness including high nuclear grade (p=1.6x10-5), presence of comedo necrosis (p=0.001) and oestrogen receptor negative (ER-)/HER2- ductal carcinoma in situ (p=4.6x10-5). Univariate analysis showed an inverse association between TXNIP expression and outcome in terms of shorter local recurrence free survival (p=0.009). Multivariable analyses showed that independent predictors of ductal carcinoma in situ recurrence were low TXNIP expression (p=0.005, HR=0.51 and 95%CI: 0.32-0.81), larger ductal carcinoma in situ size and high nuclear grade. TXNIP functions as a tumor suppressor gene with loss of its expression associated with ductal carcinoma in situ recurrence. TXNIP can be used as a potentially useful marker in prognostic stratification of ductal carcinoma in situ for management decisions.
Citation
Miligy, I. M., Gorringe, K. L., Toss, M. S., Al-Kawaz, A., Simpson, P., Diez-Rodriguez, M., …Rakha, E. (2018). Thioredoxin-interacting protein is an independent risk stratifier for breast ductal carcinoma in situ. Modern Pathology, 31(12), 1807-1815. https://doi.org/10.1038/s41379-018-0086-7
Journal Article Type | Article |
---|---|
Acceptance Date | May 23, 2018 |
Online Publication Date | Jun 28, 2018 |
Publication Date | Jun 28, 2018 |
Deposit Date | Jul 2, 2018 |
Publicly Available Date | Dec 29, 2018 |
Journal | Modern Pathology |
Print ISSN | 0893-3952 |
Electronic ISSN | 1530-0285 |
Publisher | Nature Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 31 |
Issue | 12 |
Pages | 1807-1815 |
DOI | https://doi.org/10.1038/s41379-018-0086-7 |
Keywords | Suctal carcinoma in situ; Predictor; Outcome; Progression; TXNIP, Immunohistochemistry |
Public URL | https://nottingham-repository.worktribe.com/output/942872 |
Publisher URL | https://www.nature.com/articles/s41379-018-0086-7 |
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