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首页> 外文期刊>Human Pathology >Overexpression of TNFAIP8 is associated with tumor aggressiveness and poor prognosis in patients with invasive ductal breast carcinoma
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Overexpression of TNFAIP8 is associated with tumor aggressiveness and poor prognosis in patients with invasive ductal breast carcinoma

机译:TNFAIP8的过度表达与侵袭性导管乳腺癌患者的肿瘤侵袭性和预后不良有关

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摘要

Tumor necrosis factor alpha-induced protein 8 (TNFAIP8), a transcription factor nuclear factor kappa B-inducible, antiapoptotic and oncogenic molecule, is associated with prognosis of several human malignancies. However, the relationship between TNFAIP8 and the prognosis of the invasive ductal carcinoma (IDC) of the breast remains unclear. TNFAIP8 expression was evaluated using real-time polymerase chain reaction (PCR) and Western blot analysis in 20 fresh IDC tissues and immunohistochemical analysis in 351 paraffin embedded IDC tissues. Real-time PCR and Western blot analysis demonstrated that both TNFAIP8 messenger RNA and protein were up-regulated in IDC tissues compared with the paired adjacent noncancerous tissues. Immunohistochemistry revealed that TNFAIP8 expression was significantly correlated with some clinicopathological factors, including axillary lymph node metastasis (P = .001), advanced TNM stage (P < .001), high histologic grade (P < .001), molecular subtype (P < .001), and postoperative recurrence (P < .001). Univariate and multivariate logistic regression analyses demonstrated that TNFAIP8 overexpression was strongly associated with axillary lymph node metastasis (odds ratio, 1.818; 95% confidence interval, 1.167-2.832; P = .008). Moreover, Kaplan-Meier analysis indicated that IDC patients with high TNFAIP8 expression had a shorter survival time than did those with low TNFAIP8 expression, and multivariate analysis indicated that TNFAIP8 was an independent prognostic factor for overall survival and disease-free survival in IDC (P = .041 and P = .020, respectively). Therefore, TNFAIP8 overexpression may contribute to tumor progression, and it may be a novel prognostic biomarker for the patients with IDC. (C) 2017 Elsevier Inc. All rights reserved.
机译:肿瘤坏死因子α-诱导的蛋白质8(TNFAIP8),转录因子核因子Kappa B型诱导,抗透露和致癌分子与几种人类恶性肿瘤的预后有关。然而,TNFAIP8之间的关系和乳房的侵入性导管癌(IDC)的预后仍然尚不清楚。使用实时聚合酶链反应(PCR)和20种新鲜IDC组织中的Western印迹分析和351个石蜡嵌入式IDC组织中的免疫组织化学分析评估TNFAIP8表达。实时PCR和Western印迹分析证明,与配对相邻的非癌组织相比,在IDC组织中,TNFAIP8信使RNA和蛋白质均上调。免疫组织化学发现,TNFAIP8表达与一些临床病理因子显着相关,包括腋窝淋巴结转移(P = .001),高级TNM阶段(P <.001),高组织学等学(P <.001),分子亚型(P < .001),术后复发(P <.001)。单变量和多变量逻辑回归分析证明TNFAIP8过表达与腋窝淋巴结转移强烈相关(差距比,1.818; 95%置信区间,1.167-2.832; P = .008)。此外,Kaplan-Meier分析表明,IDC具有高TNFAIP8表达的患者的存活时间较短,而不是具有低TNFAIP8表达的时间,并且多变量分析表明TNFAIP8是IDC中总存活和无病生存的独立预后因素(P = .041和p = .020)。因此,TNFAIP8过表达可能有助于肿瘤进展,并且可以是IDC患者的新预后生物标志物。 (c)2017年Elsevier Inc.保留所有权利。

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