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首页> 外文期刊>Clinical lung cancer >Serum endothelial monocyte-activating polypeptide-II: a novel biomarker in patients with non-small-cell lung cancer.
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Serum endothelial monocyte-activating polypeptide-II: a novel biomarker in patients with non-small-cell lung cancer.

机译:血清内皮单核细胞活化多肽-II:非小细胞肺癌患者的新型生物标志物。

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摘要

BACKGROUND: Endothelial monocyte-activating polypeptide-II (EMAP-II) is a proinflammatory cytokine with antiangiogenic properties. Serum EMAP-II levels have not been investigated previously in non-small-cell lung cancer (NSCLC). The aim of this study was to examine the relationship between serum EMAP-II levels and clinicopathologic features, including prognosis, in patients with NSCLC. PATIENTS AND METHODS: We measured serum EMAP-II levels in 30 healthy control subjects and 48 patients with untreated NSCLC by enzyme linkedimmunosorbent assay. RESULTS: Patients with NSCLC had significantly higher serum EMAP-II levels than did the control group (492 pg/mL +/- 1126 pg/mL vs. 266 pg/mL +/- 1013 pg/mL; P = .015). No significant association was found between serum EMAP-II levels and various clinicopathologic features (age, smoking history, performance status, histopathology, tumor stage, lymph node stage, or distant metastasis). Median survival time was 10.13 months (range, 2-53.8 months). The high-EMAP-II (>or= 100 pg/mL) group had a shorter survival compared with the low-EMAP-II (< 100 pg/mL) group (P = .023), and the serum EMAP-II level was still an important predictor of survival in a multivariate analysis, along with disease stage. CONCLUSION: Our results showed that serum EMAP-II levels are significantly higher in patients with NSCLC than in healthy subjects and suggest it is of potential prognostic value.
机译:背景:内皮单核细胞活化多肽-II(EMAP-II)是具有抗血管生成特性的促炎细胞因子。先前尚未在非小细胞肺癌(NSCLC)中研究血清EMAP-II水平。这项研究的目的是检查NSCLC患者血清EMAP-II水平与临床病理特征(包括预后)之间的关系。患者和方法:我们通过酶联免疫吸附测定法测量了30名健康对照受试者和48例未经治疗的NSCLC患者的血清EMAP-II水平。结果:NSCLC患者的血清EMAP-II水平显着高于对照组(492 pg / mL +/- 1126 pg / mL与266 pg / mL +/- 1013 pg / mL; P = .015)。血清EMAP-II水平与各种临床病理特征(年龄,吸烟史,行为状态,组织病理学,肿瘤分期,淋巴结分期或远处转移)之间未发现显着关联。中位生存时间为10.13个月(范围2-53.8个月)。高EMAP-II(>或= 100 pg / mL)组的生存期短于低EMAP-II(<100 pg / mL)组(P = .023),并且血清EMAP-II水平在多变量分析以及疾病阶段中,仍然是生存的重要预测指标。结论:我们的结果表明,NSCLC患者的血清EMAP-II水平显着高于健康受试者,表明其具有潜在的预后价值。

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