TNFAIP8 as a predictor of metastasis and a novel prognostic biomarker in patients with epithelial ovarian cancer

被引:56
作者
Liu, T. [1 ]
Gao, H. [2 ]
Chen, X. [1 ]
Lou, G. [1 ]
Gu, L. [1 ]
Yang, M. [2 ]
Xia, B. [1 ]
Yin, H. [3 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 3, Dept Gynecol, Harbin, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 3, Harbin, Peoples R China
[3] Mudanjiang Tumor Hosp, Dept Gynecol, Mudanjiang, Peoples R China
关键词
TNFAIP8; epithelial ovarian cancer; prognosis; metastasis; peritoneum; lymph node; DEATH EFFECTOR DOMAIN; CYTOREDUCTIVE SURGERY; EXPRESSION; SCC-S2; OVEREXPRESSION; IDENTIFICATION; STATISTICS; RADIATION; APOPTOSIS; GENES;
D O I
10.1038/bjc.2013.501
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: Tumour necrosis factor-alpha-induced protein 8 (TNFAIP8) has been recently documented in various malignancies, but its role in epithelial ovarian cancer (EOC) remains unknown. Methods: Tumour necrosis factor-alpha-induced protein 8 expression was determined by real-time reverse transcription PCR and western blot analysis. Tumour tissues, consisting of serous, mucinous, endometrioid and clear cell histotypes, from 202 EOC patients (International Federation of Gynecologists and Obstetricians I-IV) who underwent primary cytoreduction were collected. Then, we examined the immunohistochemical expression of TNFAIP8 and evaluated its clinical significances. Results: Tumour necrosis factor-alpha-induced protein 8 overexpression was significantly associated with high histologic grade (P = 0.005), large residual tumour size (P = 0.014), recurrence (P = 0.024) and response to chemotherapy (P < 0.001). Multivariate analysis showed that TNFAIP8 overexpression was independently correlated with the presence of lymph node (odds ratio (OR): 4.129; 95% confidence interval (CI): 1.491-11.435; P = 0.006) and intraperitoneal metastasis (OR: 2.209; 95% CI: 1.174-4.156; P = 0.014). Moreover, results revealed that the status of TNFAIP8 expression was an independently prognostic factor for both cancer-specific survival (hazard ratio (HR): 1.852; 95% CI: 1.322-2.594; P < 0.001) and disease-free survival (HR: 1.724; 95% CI: 1.235-2.407; P = 0.001) in patients with EOC. Conclusion: The present data provide evidence that TNFAIP8 predicts EOC metastasis and poor survival, highlighting its potential function as a therapeutic target for EOCs.
引用
收藏
页码:1685 / 1692
页数:8
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