Watzka Stefan B, Setinek Ulrike, Huber Monika, Cantonati Heidi, Lax Franz, Watson Sonja, Weigel Günter, Müller Michael R
Division of Thoracic Surgery, Otto Wagner Hospital, Sanatoriumstrasse 2, 1140 Vienna, Austria.
Interact Cardiovasc Thorac Surg. 2008 Feb;7(1):107-10. doi: 10.1510/icvts.2007.160473. Epub 2007 Nov 29.
Integrin-linked kinase (ILK) is a protein kinase that links integrins and growth factors to a range of signalling pathways. ILK expression and activity are increased in a variety of human cancers. However, little is known regarding the role of ILK in malignant pleural mesothelioma (MPM). In this study, we assessed the expression of ILK in samples of human MPM, and compared it with the expression of epidermal growth factor receptor (EGFR). Thirty-four samples of human malignant mesothelioma were stained with a polyclonal antibody against ILK. Two independent observers evaluated the morphological pattern and intensity of staining. The findings have been compared with the patient's characteristics. Most MPM and mesothelial cell proliferation samples (87.9%) showed cytoplasmic ILK staining of varying intensity. Normal mesothelial cells and normal lung parenchyma did not stain for ILK at all. Conversely, the percentage of positive EGFR staining was somewhat lower (75.8%). The ILK-positive patients were significantly older than the ILK-negative patients. Here we report for the first time that ILK is indeed expressed in malignant mesothelioma. For further validation of a causal association between ILK and neoplastic mesothelial transformation, these immunohistochemical results should be supplemented with clinical and molecular biological data.
整合素连接激酶(ILK)是一种蛋白激酶,它将整合素和生长因子与一系列信号通路相连。在多种人类癌症中,ILK的表达和活性都会升高。然而,关于ILK在恶性胸膜间皮瘤(MPM)中的作用却知之甚少。在本研究中,我们评估了ILK在人类MPM样本中的表达,并将其与表皮生长因子受体(EGFR)的表达进行了比较。用抗ILK的多克隆抗体对34份人类恶性间皮瘤样本进行染色。两名独立观察者评估了染色的形态模式和强度。研究结果已与患者的特征进行了比较。大多数MPM和间皮细胞增殖样本(87.9%)显示出不同强度的细胞质ILK染色。正常间皮细胞和正常肺实质根本没有ILK染色。相反,EGFR阳性染色的百分比略低(75.8%)。ILK阳性患者明显比ILK阴性患者年龄大。在此我们首次报道ILK确实在恶性间皮瘤中表达。为了进一步验证ILK与肿瘤性间皮细胞转化之间的因果关系,这些免疫组化结果应辅以临床和分子生物学数据。