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Clinical significance of serum thymus and activation-regulated chemokine in gastric cancer: Potential as a serum biomarker

机译:血清胸腺和活化调节趋化因子在胃癌中的临床意义:潜在的血清生物标志物

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摘要

Thymus and activation-regulated chemokine (TARC) can stimulate cancer cell proliferation and migration. The present study evaluated the clinical significance of serum TARC in gastric cancer (GC). We measured serum TARC, macrophage-derived chemokine, monocyte chemotactic protein-1 and stem cell factor (SCF) levels using a chemiluminescent immunoassay along the GC carcinogenesis (normal, high-risk, early GC [EGC] and advanced GC [AGC]) in both training (N = 25 per group) and independent validation datasets (90 normal, 30 high-risk, 50 EGC and 50 AGC). Serum levels were compared among groups using one-way analysis of variance. To evaluate the diagnostic potential of serum TARC for GC, receiver operating characteristic curve and logistic regression analyses were performed. Correlations between serum TARC and GC clinicopathological features were analyzed using Spearman's correlation. In the training dataset, serum TARC correlated with serum MDC, MCP-1 and SCF. However, only serum TARC and SCF were significantly higher in cancer groups than non-cancer groups (P < 0.001). In the validation dataset, serum TARC also increased along the GC carcinogenesis; the AGC group (167.2 ± 111.1 ng/mL) had significantly higher levels than the EGC (109.1 ± 67.7 ng/mL), the high-risk (66.2 ± 47.7 ng/mL) and the normal (67.5 ± 36.2 ng/mL) groups (Bonferroni, all P < 0.001). Receiver operating characteristic curves and logistic regression demonstrated the remarkable diagnostic potential of serum TARC as a single marker (72.0% sensitivity and 71.1% specificity; cutoff point, 0.37; logistic regression) and in a multiple-marker panel (72.6% sensitivity and 88.2% specificity; cutoff point, 0.54). Spearman's correlation showed that serum TARC was closely correlated with tumor size (γs = 0.227, P = 0.028), T-stage (γs = 0.340, P = 0.001), N-stage (γs = 0.318, P = 0.002) and M-stage (γs = 0.346, P = 0.001). Serum TARC is a promising serum biomarker for GC.
机译:胸腺和激活调节趋化因子(TARC)可以刺激癌细胞的增殖和迁移。本研究评估了血清TARC在胃癌(GC)中的临床意义。我们使用化学发光免疫分析法沿着GC致癌作用(正常,高风险,早期GC [EGC]和晚期GC [AGC])测量了血清TARC,巨噬细胞衍生的趋化因子,单核细胞趋化蛋白1和干细胞因子(SCF)的水平。在训练中(每组N = 25)和独立的验证数据集(90正常,30高风险,50 EGC和50 AGC)。使用单向方差分析比较各组之间的血清水平。为了评估血清TARC对GC的诊断潜力,进行了受试者工作特征曲线和logistic回归分析。使用Spearman相关性分析血清TARC与GC临床病理特征之间的相关性。在训练数据集中,血清TARC与血清MDC,MCP-1和SCF相关。但是,在癌症组中只有血清TARC和SCF显着高于非癌症组(P <0.001)。在验证数据集中,血清TARC也随着GC癌变而增加; AGC组(167.2±111.1 ng / mL)的水平明显高于EGC(109.1±67.7 ng / mL),高风险(66.2±47.7 ng / mL)和正常(67.5±36.2 ng / mL)组(邦费罗尼,所有P <0.001)。接收者操作特征曲线和逻辑回归表明,血清TARC作为单一标志物(72.0%灵敏度和71.1%特异性;临界点0.37; logistic回归)和在多个标志物组中(72.6%灵敏度和88.2%)具有显着的诊断潜力。特异性;临界点,0.54)。 Spearman的相关性表明血清TARC与肿瘤大小(γs= 0.227,P = 0.028),T期(γs= 0.340,P = 0.001),N期(γs= 0.318,P = 0.002)和M-密切相关。阶段(γs= 0.346,P = 0.001)。血清TARC是有前途的GC血清生物标志物。

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