Zhi H, Yang X J, Kuhnmuench J, Berg T, Thill R, Yang H, See W A, Becker C G, Williams C L, Li R
Department of Pathology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
J Pathol. 2009 Feb;217(3):389-97. doi: 10.1002/path.2456.
SmgGDS is a guanine nucleotide exchange factor with the unique ability to activate multiple small GTPases, implicating it in cancer development and progression. Here, we investigated the role of SmgGDS in prostate cancer by studying the expression of SmgGDS in benign and malignant prostatic tissues. We also probed SmgGDS function in three prostate carcinoma cell lines using small interfering RNA (siRNA). Immunohistochemical analysis revealed that SmgGDS levels were elevated in prostatic intraepithelial neoplasia (PIN), prostate carcinoma, and metastatic prostate carcinoma. In addition, expression of SmgGDS positively correlated with that of cyclooxygenase-2 (COX-2), a protein believed to promote the development of prostate carcinoma. Reduction of SmgGDS expression in prostate carcinoma cells inhibited proliferation and migration, irrespective of androgen receptor status. These effects were accompanied by a reduction in COX-2 expression and in activity of NF-kappaB, a known regulator of COX-2. Taken together, these findings suggest that SmgGDS promotes the development and progression of prostate cancer, possibly associated with NF-kappaB-dependent up-regulation of COX-2.
SmgGDS是一种鸟嘌呤核苷酸交换因子,具有激活多种小GTP酶的独特能力,这表明它与癌症的发生和发展有关。在此,我们通过研究SmgGDS在良性和恶性前列腺组织中的表达,探讨了SmgGDS在前列腺癌中的作用。我们还使用小干扰RNA(siRNA)在三种前列腺癌细胞系中探究了SmgGDS的功能。免疫组织化学分析显示,SmgGDS水平在前列腺上皮内瘤变(PIN)、前列腺癌和转移性前列腺癌中升高。此外,SmgGDS的表达与环氧化酶-2(COX-2)的表达呈正相关,COX-2是一种被认为促进前列腺癌发展的蛋白质。前列腺癌细胞中SmgGDS表达的降低抑制了细胞增殖和迁移,而与雄激素受体状态无关。这些作用伴随着COX-2表达的降低以及NF-κB活性的降低,NF-κB是COX-2的已知调节因子。综上所述,这些发现表明SmgGDS促进前列腺癌的发生和发展,可能与NF-κB依赖的COX-2上调有关。