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胸膜MAC30作为非小细胞肺癌伴恶性胸腔积液的预后标志物。

Pleural MAC30 as a prognostic marker in NSCLC with malignant pleural effusion.

作者信息

Shan Yi, Ding Hui, Lu Junjie, Ge Zhijun, Tan Yongfei

机构信息

Department of Critical Care Medicine, The Affiliated Yixing Hospital of Jiangsu University Yixing, Jiangsu 214200, China.

Department of Respiratory, The Affiliated Yixing Hospital of Jiangsu University Yixing, Jiangsu 214200, China.

出版信息

Oncotarget. 2017 Nov 22;8(68):112809-112815. doi: 10.18632/oncotarget.22631. eCollection 2017 Dec 22.

Abstract

Over-expressed meningioma-associate protein (MAC30) in tissues was associated with malignant tumor differentiation, metastasis and poor prognosis. However, the attention of MAC30 in pleural effusion from lung tumor is insufficient. Our retrospective study was prepared to explore the clinical values on diagnosis and prognosis of MAC30 from malignant pleural effusion (MPE) in non-small cell lung cancer (NSCLC). Levels of MAC30 were confirmed in MPE from 48 NSCLC patients and in benign pleural effusion (BPE) from 45 controls via enzyme-linked immunosorbent assay (ELISA). The association of MAC30 in MPE with clinical significance was further determined. We found that the levels of MAC30 in MPE were obviously higher than those in BPE (p < 0.05). Moreover, with a cutoff point (17.5 ng/ml), we confirmed the sensitivity and specificity of MAC30 for MPE were 82.7% and 85.3% using ROC curve analysis. Indeed, longer overall survival (OS) was present in NSCLC patients with low MAC30 expression in MPE. Multivariate analysis explicated that elevated MAC30 in MPE was an independent prognostic factor for shorter OS of NSCLC. Our data suggests that MAC30 in pleural effusion could be a potential prognostic marker in NSCLC with MPE.

摘要

组织中过表达的脑膜瘤相关蛋白(MAC30)与恶性肿瘤分化、转移及预后不良相关。然而,MAC30在肺癌胸腔积液中的研究关注度不足。我们的回顾性研究旨在探讨MAC30在非小细胞肺癌(NSCLC)恶性胸腔积液(MPE)诊断及预后中的临床价值。通过酶联免疫吸附测定(ELISA)法检测了48例NSCLC患者MPE及45例对照者良性胸腔积液(BPE)中MAC30的水平,并进一步确定MPE中MAC30与临床意义的相关性。我们发现MPE中MAC30水平明显高于BPE(p < 0.05)。此外,通过ROC曲线分析,以临界值17.5 ng/ml确定MAC30对MPE的敏感性和特异性分别为82.7%和85.3%。事实上,MPE中MAC30表达低的NSCLC患者总生存期(OS)更长。多因素分析表明,MPE中MAC30升高是NSCLC患者OS缩短的独立预后因素。我们的数据表明,胸腔积液中的MAC30可能是NSCLC合并MPE的潜在预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27de/5762552/887968ee1655/oncotarget-08-112809-g001.jpg

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