Abstract | BACKGROUND: We previously identified estrogen-responsive finger protein (Efp) as an estrogen-induced gene, and showed that the positive immunoreactivity of Efp is a poor prognostic factor for patients with breast cancer. We also demonstrated that Efp has distinctive roles in innate immunity by activating pattern recognition receptor retinoic acid-inducible gene I (RIG-I). The clinical value of RIG-I protein expression in breast cancer had not been evaluated in relationship with patients' prognosis. PATIENTS AND METHODS: RESULTS: Positive immunoreactivity of RIG-I was correlated with lower disease-free survival (P = .032) and was an independent poor prognostic factor (P = .043). RIG-I immunoreactivity was positively correlated with that of Efp (P = .0004). Patients with positive immunoreactivities of both RIG-I and Efp proteins were associated with a lower disease-free survival rate (P = .005). CONCLUSIONS: Positive immunoreactivity of RIG-I has clinical significance as a poor prognostic factor in patients with estrogen receptor-positive breast cancer. A positive correlation of RIG-I and Efp immunoreactivities was observed, and the combination of their immunoreactivities can be used to predict patients' prognosis.
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Authors | Junichiro Sato, Kotaro Azuma, Keiichi Kinowaki, Kazuhiro Ikeda, Takuya Ogura, Yutaka Takazawa, Hidetaka Kawabata, Masanobu Kitagawa, Satoshi Inoue |
Journal | Clinical breast cancer
(Clin Breast Cancer)
Vol. 21
Issue 5
Pg. 399-407.e2
(10 2021)
ISSN: 1938-0666 [Electronic] United States |
PMID | 33386231
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2020 Elsevier Inc. All rights reserved. |
Chemical References |
- Biomarkers, Tumor
- Transcription Factors
- Tripartite Motif Proteins
- TRIM25 protein, human
- Ubiquitin-Protein Ligases
|
Topics |
- Biomarkers, Tumor
(metabolism)
- Breast Neoplasms
(metabolism, pathology)
- Cell Line, Tumor
- Female
- Humans
- Prognosis
- Transcription Factors
(metabolism)
- Tripartite Motif Proteins
(metabolism)
- Ubiquitin-Protein Ligases
(metabolism)
|