Marchetti Antonio, Tinari Nicola, Buttitta Fiamma, Chella Antonio, Angeletti Carlo Alberto, Sacco Rocco, Mucilli Felice, Ullrich Axel, Iacobelli Stefano
Department of Oncology and Neurosciences, University G. D'Annunzio, Chieti, Italy 66100.
Cancer Res. 2002 May 1;62(9):2535-9.
90K, also known as Mac-2 binding protein, is a secreted glycoprotein that binds galectins, beta1-integrins, collagens, and fibronectin, and has some relevance in cell-cell and cell-extracellular matrix adhesion. Previous studies have shown that serum levels of 90K have prognostic value in several neoplasms. In the present study, the role of the expression of 90K as an adverse prognostic indicator in 72 pathological stage I non-small cell lung cancer patients was investigated immunohistochemically. All of the patients underwent complete surgical removal of the tumor. The median length of follow-up care was 54 months. High level of 90K expression (90K staining of > or =50% of the neoplastic cells) was observed in 20 of the 72 (28%) tumors. Expression of 90K was confirmed by ELISA. The results showed that a high expression of 90K correlates with adverse prognosis. Among patients with high 90K expression, the disease-free and overall survival rates were significantly lower than the same rates of those with low expression (P = 0. 0001 and P = 0. 0003, respectively). The incidence of distant metastases in the patients with high 90K expression (60%; 12 of 20 patients) was significantly higher than that of in the patients with low expression (21%; 11 of 53 patients; P = 0.0038). The results of multivariate analysis confirmed that a high 90K expression was a significant factor to predict poor prognosis. We suggest that 90K expression could be a useful prognostic factor in patients with stage I non-small cell lung cancer, likely as an indicator of the metastatic propensity of the tumor.
90K,也被称为Mac-2结合蛋白,是一种分泌型糖蛋白,可与半乳糖凝集素、β1整合素、胶原蛋白和纤连蛋白结合,在细胞间和细胞与细胞外基质黏附中具有一定作用。先前的研究表明,90K的血清水平在几种肿瘤中具有预后价值。在本研究中,采用免疫组织化学方法研究了90K表达作为72例病理I期非小细胞肺癌患者不良预后指标的作用。所有患者均接受了肿瘤的完整手术切除。随访护理的中位时长为54个月。在72例肿瘤中的20例(28%)中观察到90K高表达(90K染色的肿瘤细胞≥50%)。通过酶联免疫吸附测定法(ELISA)证实了90K的表达。结果显示,90K的高表达与不良预后相关。在90K高表达的患者中,无病生存率和总生存率显著低于低表达患者(分别为P = 0.0001和P = 0.0003)。90K高表达患者的远处转移发生率(60%;20例患者中的12例)显著高于低表达患者(21%;53例患者中的11例;P = 0.0038)。多因素分析结果证实,90K高表达是预测不良预后的重要因素。我们认为,90K表达可能是I期非小细胞肺癌患者有用的预后因素,可能作为肿瘤转移倾向的指标。