Rta-IgG as a biomarker for diagnosis and post treatment prognostic of nasopharyngeal carcinoma

Rta-IgG as a biomarker for diagnosis and post treatment prognostic of nasopharyngeal carcinoma
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Rta-IgG作为鼻咽癌诊断和治疗后预后的生物标志物

DOI:
10.3233/cbm-160586
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发表时间:
2016-01-01
期刊:
影响因子:
3.1
通讯作者:
Guo, Lin
Guo, Lin
中科院分区:
医学3区
文献类型:
--
作者:
Xu, Xiao-Feng;Lu, Ren-Quan;Guo, Lin

文献摘要

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背景技术背景:鼻咽癌(Nasopharyngeal carcinoma,NPC)是一种常见的头颈部恶性肿瘤。目的:检测未经治疗的NPC患者血清中EB病毒Rta蛋白的表达,并比较NPC患者血清中Rta-IgG和VCA-IgA的差异。在目前的工作中,收集13例未经治疗的鼻咽癌患者和10例非鼻咽癌对照的鼻咽组织进行免疫组化(IHC),染色分析Rta蛋白的表达水平,同时制备血清标本,采用酶联免疫吸附试验(ELISA)检测Rta-IgG水平对鼻咽癌患者、其他肿瘤患者及正常人的诊断价值。对26例鼻咽癌患者治疗前后及治疗后1 ~ 2年的血清Rta-IgG水平进行监测。Rta蛋白在鼻咽癌组和非鼻咽癌组中的表达差异有统计学意义(P < 0.05)。相应地,NPC患者血清Rta-IgG水平(3.05,1.19-4.95)明显高于非NPC参与者(0.15,0.08-0.30,P < 0.05)包括肺癌患者(0.14,0.08-0.19),乳腺癌患者(0.17,0.10-0.25),胃癌患者(0.08,0.05-0.16),恶性淋巴瘤患者鼻咽良性病变组(1.65,0.74-1.93)和健康志愿者组(0.22,0.13-0.32)。受试者操作特征(ROC)分析结果表明,Rta-IgG诊断鼻咽癌的敏感性为83.6%,特异性为82.4%,其诊断效率高于VCA-IgA。Rta-IgG阳性率与临床分期有关,与转移部位无关。结论:鼻咽癌患者血清Rta表达水平升高,血清Rta-IgG可作为鼻咽癌鉴别诊断和疗效监测的生物标志物。
BACKGROUND: Nasopharyngeal carcinoma (NPC) is a common type of head and neck cancer.OBJECTIVE: This study aimed to detect the expression of Epstein-Barr viral Rta protein in patients with untreated NPC, and compare the serum Rta-IgG with the VCA-IgA in patients with NPC.METHODS: In the current work, the nasopharyngeal tissues of untreated NPC patients (n = 13) and non-NPC controls (n = 10) were collected for the immunohistochemical (IHC) staining to analyze the levels of Rta protein expression, meanwhile serum samples from the participants were prepared to assess the roles of Rta-IgG level with Enzyme-linked immunosorbence assay (ELISA) in diagnosis of NPC including the patients with NPC, the patients with other cancers, and normal volunteers.RESULTS: The levels of serum Rta-IgG in 26 NPC patients were monitored at pre-and post-treatments, as well as one to two year after. We found that there was a significant difference of the expression levels of Rta protein between NPC and non-NPC groups (P < 0.05). Correspondingly, the levels of serum Rta-IgG in NPC patients (3.05, 1.19-4.95) were significantly higher than those of non-NPC participants (0.15, 0.08-0.30, P < 0.05) including the patients with lung cancer (0.14, 0.08-0.19), the patients with breast carcinoma (0.17, 0.10-0.25), the patients with gastric carcinoma (0.08, 0.05-0.16), the patients with malignant lymphoma (0.13, 0.08-0.20), the patients with benign nasopharyngeal disease (1.65, 0.74-1.93) and healthy volunteers (0.22, 0.13-0.32), respectively. With a receiver operation characteristic (ROC) analysis, the cut-off value to discriminate NPC patients from the controls was established at 0.92 (S/CO) for Rta-IgG (sensitivity 83.6%; specificity 82.4%), the diagnosis efficacy of Rta-IgG was higher than VCA-IgA. The positive rates of Rta-IgG were related to clinical stage, but not metastatic sites. Serum concentrations of Rta-IgG were decreased in NPC patients with effective radiation, and slightly raised or with no change with ineffective radiation.CONCLUSIONS: Rta expression levels are elevated in the patients with NPC, and serum Rta-IgG is a promising biomarker in both differential diagnosis and therapy-monitoring of the patients with NPC.