4.7 Article

miR-372 suppresses tumour proliferation and invasion by targeting IGF2BP1 in renal cell carcinoma

期刊

CELL PROLIFERATION
卷 48, 期 5, 页码 593-599

出版社

WILEY
DOI: 10.1111/cpr.12207

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资金

  1. National Nature Science Foundation of China [81301964]
  2. Postgraduate Student Foundation for New Teacher from the Ministry of Education of China [20133601120013]
  3. Foundation from Department of Education of Jiangxi Province [GJJ14215, GJJ14194]
  4. Province National Natural Science Foundation of Jiangxi [20151BAB215023]
  5. Foundation for Post-Doctor Research Project of Jiangxi Province, China

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ObjectivesMicroRNAs (miRNAs) are endogenous small non-coding RNAs that regulate proteins and mRNAs for degradation or translational suppression. Up to now, the role of miR-372 in renal cell carcinoma has remained unknown; in this study, we have aimed to reveal its functional importance in this tumour. Materials and methodsqRT-PCR was performed to measure expression levels of miR-372 in renal cell carcinoma cell lines and tissues. CCK-8 and an invasion assay were performed to measure its functional role. Luciferase assays, qRT-PCR and western blotting were performed to discover miR-372s target gene. ResultsWe demonstrated that miRNA-372 was down-regulated in renal cell carcinoma cell lines and tissue specimens; its over-expression inhibited cell proliferation and invasion. Moreover, we showed that miRNA-372 repressed insulin-like growth factor 2 mRNA-binding protein 1 (IGF2BP1) expression by directly interacting with its putative binding site at the 3-UTR. Furthermore, ectopic expression of IGF2BP1 significantly reversed suppression of cell proliferation and invasion caused by miR-372 over-expression. ConclusionsOur data indicated that miR-372 seemed to function as a tumour suppressor in renal cell carcinoma progression by inhibiting the IGF2BP1 expression.

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