Journal
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume 458, Issue 4, Pages 816-822Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2015.02.037
Keywords
Autophagy; ATG5; FIP200; Breast cancer; Disease-free survival
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Funding
- National Natural Science Foundation of China [81202082, 81201531]
- Shanghai Committee of Science and Technology Funds [12ZR1406200, 12DZ2260100, 12410707700, 12140901502]
- Shanghai Committee of Science and Technology Fund [11QA1401400]
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Autophagy is a self-digesting process that is primarily responsible for the removal and recycling of longlived proteins and damaged organelles to maintain the homeostasis of the cell. Recent studies have indicated dual roles for autophagy in cancer: suppression of tumor progression and promotion of survival. In this study, we sought to investigate the prognostic value of two autophagy-related proteins, autophagy-related gene 5 (ATG5) and FAK family kinase-interacting protein of 200 kDa (FIP200), in patients with operable breast cancer. More specifically, the expression of ATG5 and FIP200 was evaluated by immunohistochemistry (IHC) in surgical specimens collected from 200 patients who were diagnosed with histologically proven invasive ductal breast cancer. A stepwise Cox multivariate analysis was then performed to construct a risk prediction model. In this retrospective cohort study, both ATG5 (HR = 0.465, 95% Cl 0.247-0.872, P = 0.017) and FIP200 (HR = 0.521, 95% Cl 0.278-0.979, P = 0.043) correlated with prolonged disease-free survival (DES). In a receiver operating characteristic (ROC) analysis, the addition of ATG5 and FIP200 expression led to a significantly improved area under the timedependent ROC curve (AUC) at 3 years (0.748 versus 0.680, P < 0.001) and 5 years (0.756 versus 0.699, P < 0.001). Collectively, our findings established the prognostic significance of ATG5 and FIP200 in patients with breast cancer. (C) 2015 Elsevier Inc. All rights reserved.
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