Hiendlmeyer Elke, Regus Susanne, Wassermann Stella, Hlubek Falk, Haynl Angela, Dimmler Arno, Koch Claudia, Knoll Claudia, van Beest Moniek, Reuning Ute, Brabletz Thomas, Kirchner Thomas, Jung Andreas
Pathologisches Institut der Universität Erlangen-Nürnberg, Krankenhausstrasse 8-10, 91054 Erlangen, Germany.
Cancer Res. 2004 Feb 15;64(4):1209-14. doi: 10.1158/0008-5472.can-3627-2.
Expression of the urokinase plasminogen activator (uPA) increases during the progression of colorectal tumors from adenomas to carcinomas. The highest amounts of uPA are found at the invasion front of carcinomas, which also displays a strong expression of nuclear beta-catenin and is therefore a region expressing beta-catenin target genes at high levels. Here we show that beta-catenin contributes to the transactivation of uPA. Therefore, beta-catenin might have an impact on the capacity of colorectal tumors for invasion and metastasis, as well as dormancy, which are hallmarks of cancer.
在结直肠癌从腺瘤发展为癌的过程中,尿激酶型纤溶酶原激活剂(uPA)的表达会增加。在癌的侵袭前沿发现uPA的含量最高,该区域还显示出强烈的核β-连环蛋白表达,因此是高水平表达β-连环蛋白靶基因的区域。在此我们表明,β-连环蛋白有助于uPA的反式激活。因此,β-连环蛋白可能会对结直肠癌的侵袭、转移以及休眠能力产生影响,而这些都是癌症的特征。