Department of Gynecology, The Third Affiliated Hospital, Harbin Medical University, Harbin, China.
Br J Cancer. 2013 Sep 17;109(6):1685-92. doi: 10.1038/bjc.2013.501. Epub 2013 Aug 27.
Tumour necrosis factor-α-induced protein 8 (TNFAIP8) has been recently documented in various malignancies, but its role in epithelial ovarian cancer (EOC) remains unknown.
Tumour necrosis factor-α-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.
Tumour necrosis factor-α-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.
The present data provide evidence that TNFAIP8 predicts EOC metastasis and poor survival, highlighting its potential function as a therapeutic target for EOCs.
肿瘤坏死因子-α诱导蛋白 8(TNFAIP8)最近在各种恶性肿瘤中被记录,但它在卵巢上皮癌(EOC)中的作用尚不清楚。
通过实时逆转录 PCR 和 Western blot 分析确定肿瘤坏死因子-α诱导蛋白 8 的表达。收集了 202 名接受初次细胞减灭术的 EOC 患者(国际妇产科联合会 I-IV 期)的肿瘤组织,包括浆液性、黏液性、子宫内膜样和透明细胞组织型。然后,我们检查了 TNFAIP8 的免疫组织化学表达,并评估了其临床意义。
TNFAIP8 的过度表达与高组织学分级(P=0.005)、大残余肿瘤大小(P=0.014)、复发(P=0.024)和对化疗的反应(P<0.001)显著相关。多变量分析表明,TNFAIP8 的过度表达与淋巴结存在(优势比(OR):4.129;95%置信区间(CI):1.491-11.435;P=0.006)和腹腔内转移(OR:2.209;95% CI:1.174-4.156;P=0.014)独立相关。此外,结果表明 TNFAIP8 表达状态是 EOC 患者癌症特异性生存(风险比(HR):1.852;95% CI:1.322-2.594;P<0.001)和无病生存(HR:1.724;95% CI:1.235-2.407;P=0.001)的独立预后因素。
本研究数据提供了证据表明 TNFAIP8 预测 EOC 转移和不良生存,强调了其作为 EOC 治疗靶点的潜在功能。