Scholz Claus-Jürgen, Kurzeder Christian, Koretz Karin, Windisch Jasmin, Kreienberg Rolf, Sauer Georg, Deissler Helmut
IZKF Laboratory for Microarray Applications, University of Würzburg, Germany.
Cancer Lett. 2009 Mar 18;275(2):198-203. doi: 10.1016/j.canlet.2008.10.014. Epub 2008 Nov 18.
In many human cancers, tumor progression was found to be associated with an altered expression of tetraspanins, a group of transmembrane adaptor proteins that are implicated in fundamental cellular processes. Although recognized as a characteristic of malignant cells of various origins, Tspan-1 has not yet been characterized in detail due to lack of specific antibodies. We describe the generation of Tspan-1-specific antibodies and immunohistochemical staining of different subtypes of ovarian carcinomas (n=72) that revealed significant differences in Tspan-1 expression that was pronounced in mucinous and endometrioid tumors. The observation that immunoreactivity was focused in intracellular vesicles often concentrated at the luminal sides of glandular structures further supported the assumption that Tspan-1 is involved in secretory pathways. In the group of serous ovarian carcinomas, pronounced expression of Tspan-1 was observed in FIGO stage III C-classified tumors of advanced stages. In summary, our results show that Tspan-1 is an important characteristic of malignant ovarian cancer cells and a potential therapeutic target.
在许多人类癌症中,肿瘤进展被发现与四跨膜蛋白的表达改变有关,四跨膜蛋白是一组参与基本细胞过程的跨膜衔接蛋白。尽管Tspan-1被认为是各种起源的恶性细胞的一个特征,但由于缺乏特异性抗体,尚未对其进行详细表征。我们描述了Tspan-1特异性抗体的产生以及对72例不同亚型卵巢癌的免疫组织化学染色,结果显示Tspan-1表达存在显著差异,在黏液性和子宫内膜样肿瘤中尤为明显。免疫反应集中在细胞内小泡且常聚集在腺结构腔面的观察结果进一步支持了Tspan-1参与分泌途径的假设。在浆液性卵巢癌组中,在国际妇产科联盟(FIGO)III C期分类的晚期肿瘤中观察到Tspan-1的明显表达。总之,我们的结果表明Tspan-1是恶性卵巢癌细胞的一个重要特征和潜在的治疗靶点。