首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Serum macrophage migration-inhibitory factor as a diagnostic and prognostic biomarker for gastric cancer.
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Serum macrophage migration-inhibitory factor as a diagnostic and prognostic biomarker for gastric cancer.

机译:血清巨噬细胞迁移抑制因子作为胃癌的诊断和预后生物标志物。

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BACKGROUND: This study aimed to determine the potential diagnostic value of migration-inhibitory factor (MIF) for gastric cancer in patients presenting with dyspepsia and its prognostic value for gastric cancer. METHODS: A cohort of 97 patients with histologically confirmed gastric adenocarcinoma and 222 patients with dyspepsia were recruited. Enzyme-linked immunosorbent assay was used to measure serum MIF and carcinoembryonic antigen (CEA). RESULTS: The serum MIF concentrations were 6554.0 +/- 204.1 pg/mL and 1453.7 +/- 79.9 pg/mL, respectively, in gastric cancer patients and dyspeptic patients (P < .001). Serum MIF levels increased with the advancing gastric pathologies (P < .001). With the cutoff value of 3230 pg/mL, serum MIF had sensitivity, specificity, and accuracy of 83.5%, 92.3%, and 89.7%, respectively, in diagnosing gastric cancer, whereas the rates were 60.8%, 83.3%, and 76.5%, respectively, for serum CEA. Gastric cancer patients with serum MIF levels above 6600 pg/mL had a lower 5-year survival rate than those with serum MIF level below that level (P = .012). Higher serum CEA levels were also associated with poor survival. The prediction for 5-year survival was even better (P = .0001), using a combination of serum MIF and CEA. CONCLUSIONS: Serum MIF level, which correlates with gastric MIF expression, is a better molecular marker than CEA in diagnosing gastric cancer in patients presenting with dyspepsia. A combination of serum MIF and CEA predicts 5-year survival better than the individual test.
机译:背景:这项研究旨在确定迁移抑制因子(MIF)对消化不良患者的胃癌的潜在诊断价值及其对胃癌的预后价值。方法:招募了97例经组织学证实为胃腺癌的患者和222例消化不良的患者。酶联免疫吸附法用于测定血清MIF和癌胚抗原(CEA)。结果:胃癌患者和消化不良患者的血清MIF浓度分别为6554.0 +/- 204.1 pg / mL和1453.7 +/- 79.9 pg / mL(P <.001)。血清MIF水平随着胃部疾病的进展而增加(P <.001)。血清MIF的临界值为3230 pg / mL,在胃癌诊断中的敏感性,特异性和准确性分别为83.5%,92.3%和89.7%,而检出率分别为60.8%,83.3%和76.5%。分别用于血清CEA。血清MIF高于6600 pg / mL的胃癌患者的5年生存率低于血清MIF低于该水平的患者(P = 0.012)。血清CEA水平升高也与存活率低有关。使用血清MIF和CEA的组合,对5年生存的预测甚至更好(P = .0001)。结论:与胃癌MIF表达相关的血清MIF水平在诊断消化不良患者的胃癌中比CEA更好。血清MIF和CEA的组合比单独测试预测的5年生存率更好。

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