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MAC30表达在人肺纯鳞状细胞癌中的预后价值

Prognostic Value of MAC30 Expression in Human Pure Squamous Cell Carcinomas of the Lung.

作者信息

Ding Hui, Gui Xian-Hua, Lin Xu-Bo, Chen Ru-Hua, Cai Hou-Rong, Fen Yan, Sheng Yun-Lu

机构信息

Department of Respiratory Medicine, Yixing People Hospital, Affiliated Jiangsu University, Nanjing, China E-mail :

出版信息

Asian Pac J Cancer Prev. 2016;17(5):2705-10.

Abstract

Recent evidence haas indicated that meningioma-associate protein (MAC30) exhibits different expression patterns in various tumors. However, little is known about the value of MAC30 in human squamous cell carcinoma of lung (SQCLC). The purpose of our study was to investigate the expression of MAC30 and to explore its clinical significance in SQCLC patients. A total of 156 Chinese patients diagnosed with SQCLC were selected for this study. The expression of MAC30 in all tissues was confirmed by immunohistochemical staining. Quantitative real-time PCR was performed to analyze MAC30 mRNA expression in 32 cases of SQCLC patients with corresponding non-tumor lung tissues. We observed enhanced mRNA expression of MAC30 in SQCLC as compared to control samples. Further, elevated MAC30 protein expression was strongly associated with poor tumor differentiation, TNM stage, and lymph node metastasis. In addition, we observed that patients with increased MAC30 expression demonstrated poor overall survival. Multivariate analysis explicated that increased MAC30 expression was a valuable independent predictable factor for poor tumor differentiation and short survival in SQCLC patients. Our present study suggests that MAC30 may serve as a biomarker for poor tumor differentiation and outcomes of patients with SQCLC.

摘要

最近的证据表明,脑膜瘤相关蛋白(MAC30)在各种肿瘤中表现出不同的表达模式。然而,关于MAC30在人肺鳞状细胞癌(SQCLC)中的价值知之甚少。我们研究的目的是调查MAC30的表达,并探讨其在SQCLC患者中的临床意义。本研究共选取了156例诊断为SQCLC的中国患者。通过免疫组织化学染色确认所有组织中MAC30的表达。对32例SQCLC患者及其相应的非肿瘤肺组织进行定量实时PCR分析MAC30 mRNA表达。我们观察到与对照样本相比,SQCLC中MAC30的mRNA表达增强。此外,MAC30蛋白表达升高与肿瘤低分化、TNM分期及淋巴结转移密切相关。此外,我们观察到MAC30表达增加的患者总生存期较差。多因素分析表明,MAC30表达增加是SQCLC患者肿瘤低分化和生存期短的一个有价值的独立预测因素。我们目前的研究表明,MAC30可能作为SQCLC患者肿瘤低分化和预后的生物标志物。

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