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首页> 外文期刊>BMC Cancer >Plasma secretory phospholipase A2-IIa as a potential biomarker for lung cancer in patients with solitary pulmonary nodules
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Plasma secretory phospholipase A2-IIa as a potential biomarker for lung cancer in patients with solitary pulmonary nodules

机译:血浆分泌性磷脂酶A2-IIa作为孤立性肺结节患者肺癌的潜在生物标志物

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Background Five-year survival for lung cancer has remained at 16% over last several decades largely due to the fact that over 50% of patients are diagnosed with locally-advanced or metastatic disease. Diagnosis at an earlier and potentially curable stage is crucial. Solitary pulmonary nodules (SPNs) are common, but the difficulty lies in the determination of which SPN is malignant. Currently, there is no convenient and reliable biomarker effective for early diagnosis. Secretory phospholipase A2-IIa (sPLA2-IIa) is secreted into the circulation by cancer cells and may allow for an early detection of lung cancer. Methods Plasma samples from healthy donors, patients with only benign SPN, and patients with lung cancer were analyzed. Expression of sPLA2-IIa protein in lung cancer tissues was also determined. Results We found that the levels of plasma sPLA2-IIa were significantly elevated in lung cancer patients. The receiver operating characteristic curve analysis, comparing lung cancer patients to patients with benign nodules, revealed an optimum cutoff value for plasma sPLA2-IIa of 2.4 ng/ml to predict an early stage cancer with 48% sensitivity and 86% specificity and up to 67% sensitivity for T2 stage lung cancer. Combined sPLA2-IIa, CEA, and Cyfra21.1 tests increased the sensitivity for lung cancer prediction. High level of plasma sPLA2-IIa was associated with a decreased overall cancer survival. sPLA2-IIa was overexpressed in almost all non-small cell lung cancer and in the majority of small cell lung cancer by immunohistochemistry analysis. Conclusion Our finding strongly suggests that plasma sPLA2-IIa is a potential lung biomarker to distinguish benign nodules from lung cancer and to aid lung cancer diagnosis in patients with SPNs.
机译:背景技术在过去的几十年中,肺癌的五年生存率一直保持在16%,这主要是由于超过50%的患者被诊断出患有局部晚期或转移性疾病。在早期且可能治愈的阶段进行诊断至关重要。孤立性肺结节(SPN)很常见,但困难在于确定哪个SPN是恶性的。当前,尚没有有效且可靠的早期诊断生物标记物。分泌型磷脂酶A2-IIa(sPLA2-IIa)被癌细胞分泌到循环系统中,可以早期发现肺癌。方法分析来自健康供体,仅良性SPN患者和肺癌患者的血浆样本。还确定了sPLA2-IIa蛋白在肺癌组织中的表达。结果我们发现肺癌患者血浆sPLA2-IIa的水平显着升高。接收器工作特性曲线分析将肺癌患者与良性结节患者进行了比较,发现血浆sPLA2-IIa的最佳临界值为2.4 ng / ml,可预测早期癌症,其敏感性为48%,特异性为86%,最高可达67对T2期肺癌的%敏感性。结合使用sPLA2-IIa,CEA和Cyfra21.1测试可提高肺癌预测的敏感性。血浆sPLA2-IIa的高水平与总体癌症生存率降低有关。通过免疫组织化学分析,sPLA2-IIa在几乎所有非小细胞肺癌和大多数小细胞肺癌中均过表达。结论我们的发现强烈表明血浆sPLA2-IIa是一种潜在的肺生物标志物,可将良性结节与肺癌区分开,并有助于SPN患者的肺癌诊断。

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