Suppr超能文献

微小 RNA-145 靶向金属蛋白酶 ADAM17,在肾细胞癌患者中受到抑制。

MicroRNA-145 targets the metalloprotease ADAM17 and is suppressed in renal cell carcinoma patients.

机构信息

Pharmazentrum Frankfurt/Zentrum für Arzneimittelforschung, Entwicklung und Sicherheit, Goethe University Hospital, Frankfurt am Main, Germany.

出版信息

Neoplasia. 2013 Feb;15(2):218-30. doi: 10.1593/neo.121222.

Abstract

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.

摘要

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。

相似文献

5
MicroRNA-152 targets ADAM17 to suppress NSCLC progression.MicroRNA-152 靶向 ADAM17 抑制非小细胞肺癌进展。
FEBS Lett. 2014 May 21;588(10):1983-8. doi: 10.1016/j.febslet.2014.04.022. Epub 2014 Apr 26.

引用本文的文献

本文引用的文献

8
New role of microRNA: carcinogenesis and clinical application in cancer.微小 RNA 的新角色:致癌作用及在癌症中的临床应用。
Acta Biochim Biophys Sin (Shanghai). 2011 Nov;43(11):831-9. doi: 10.1093/abbs/gmr080. Epub 2011 Sep 10.
9
ADAM17: a molecular switch to control inflammation and tissue regeneration.ADAM17:控制炎症和组织再生的分子开关。
Trends Immunol. 2011 Aug;32(8):380-7. doi: 10.1016/j.it.2011.05.005. Epub 2011 Jul 13.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验