| Literature DB >> 30537206 |
Yanfa He1, Jianzhen Liu2, Yongjun Wang3, Xiaoli Zhu2, Zhengchao Fan2, Chongbin Li2, Hang Yin2, Ying Liu4.
Abstract
Renal cell carcinoma (RCC) is a common kidney tumor in adults. The role of miR-486-5p in RCC is unknown. The aim of our study was to identify new targets regulated by miR-486-5p in RCC, to obtain a deeper insight into the network and to better understand the role of these microRNAs and their targets in carcinogenesis of RCC. We performed a series of tests and found consistently lower expression levels of miR-486-5p in kidney cancer cells. Restoration of miR-486-5p expression in RCC cells could lead to the suppression of cell proliferation and the increase of cell apoptosis. Further studies demonstrated that TGF-β-activated kinase 1 was a target gene of miR-486-5p in kidney cancer cells. It was also shown that C-C motif chemokine ligand 2 (CCL2) from tumor-associated macrophages downregulated miR-486-5p expression, and miR-486-5p inhibited RCC cell proliferation and apoptosis resistance induced by CCL2. The study demonstrates that there are potential diagnosis and therapy values of miR-486-5p in RCC.Entities:
Keywords: C-C motif chemokine ligand 2 (CCL2); TGF-β-activated kinase 1 (TAK1); apoptosis; miR-486-5p; renal cell carcinoma
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Year: 2018 PMID: 30537206 DOI: 10.1002/jcb.26900
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429