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MicroRNA-145 Targets the Metalloprotease ADAM17 and Is Suppressed in Renal Cell Carcinoma Patients

Authors :
Kai Doberstein
Nico Steinmeyer
Ann-Kathrin Hartmetz
Wolfgang Eberhardt
Michel Mittelbronn
Patrick N. Harter
Eva Juengel
Roman Blaheta
Josef Pfeilschifter
Paul Gutwein
Source :
Neoplasia: An International Journal for Oncology Research, Vol 15, Iss 2, Pp 218-230 (2013)
Publication Year :
2013
Publisher :
Elsevier, 2013.

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.

Details

Language :
English
ISSN :
14765586 and 15228002
Volume :
15
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Neoplasia: An International Journal for Oncology Research
Publication Type :
Academic Journal
Accession number :
edsdoj.f4b2e17e8f94f12b8b8feaa96d6cefd
Document Type :
article
Full Text :
https://doi.org/10.1593/neo.121222