Pharmazentrum Frankfurt/Zentrum für Arzneimittelforschung, Entwicklung und Sicherheit, Goethe University Hospital, Frankfurt am Main, Germany.
Neoplasia. 2013 Feb;15(2):218-30. doi: 10.1593/neo.121222.
A disintegrin and metalloproteinase 17 (ADAM17) is a metalloprotease that is overexpressed in many cancer types, including renal cancers. However, the regulatory mechanisms of ADAM17 in cancer development and progression are poorly understood. In the present work, we provide evidence using overexpression and inhibition of microRNA 145 (miR-145) that miR-145 negatively regulates ADAM17 expression. Furthermore, we show that ADAM17 negatively regulates miR-145 through tumor necrosis factor-α, resulting in a reciprocal negative feedback loop. In this study, the expression of ADAM17 and miR-145 correlated negatively in renal cancer tumor tissues and cell lines, suggesting an important regulatory mechanism. Additionally, we showed that the regulation of ADAM17 is partly involved in the effects of miR-145 on proliferation and migration, whereas no involvement in chemosensitivity was observed. Importantly, in the healthy kidney, miR-145 was detected in different cell types including tubular cells, which are considered the origin of renal cancer. In renal cancer cell lines, miR-145 expression was strongly suppressed by methylation. In summary, miR-145 is downregulated in renal cancer patients, which leads to the up-regulation of ADAM17 in renal cancer. Importantly, miR-145 and ADAM17 are regulated in a reciprocal negative feedback loop.
解整合素金属蛋白酶 17(ADAM17)是一种在许多癌症类型中过度表达的金属蛋白酶,包括肾癌。然而,ADAM17 在癌症发展和进展中的调节机制尚不清楚。在本工作中,我们通过 miRNA 145(miR-145)的过表达和抑制实验提供了证据,表明 miR-145 负调控 ADAM17 的表达。此外,我们表明 ADAM17 通过肿瘤坏死因子-α(tumor necrosis factor-α)负调控 miR-145,导致一个相互的负反馈回路。在这项研究中,ADAM17 和 miR-145 的表达在肾癌肿瘤组织和细胞系中呈负相关,提示存在重要的调节机制。此外,我们表明 ADAM17 的调节部分涉及 miR-145 对增殖和迁移的影响,而对化疗敏感性没有影响。重要的是,在健康的肾脏中,miR-145 在不同的细胞类型中被检测到,包括被认为是肾癌起源的管状细胞。在肾癌细胞系中,miR-145 的表达被甲基化强烈抑制。总之,miR-145 在肾癌患者中下调,导致 ADAM17 在肾癌中的上调。重要的是,miR-145 和 ADAM17 受到相互的负反馈调节。