科研之友
微信
新浪微博
Facebook
分享链接
摘要
Objective: To identify microRNA s (miRNA s) that are overexpressed in renal cell carcinoma (RC) and characterize the functional role of miR-21. Materials and methods: The miRNA expression profiles between RC tissue and adjacent normal tissue were compared using microarray analysis. The differential expression of miR-21 was validated by real-time polymerase chain reaction (RT-PCR). 786-O RC cells were transfected with miR-21 mimic, miR-21 inhibitor, or negative controls and cell proliferation, apoptosis and cell cycle were examined by MTT assay and flow cytometry. The expression of programmed cell death 4 (PDCD4) and tropomyosin 1 (TPM1) was detected by RT-PCR and Western blot analysis. Results: Compared to adjacent normal tissue, 10 human miRNA s were significantly upregulated and 7 were downregulated in RC tissue. RT-PCR confirmed that miR-21 was significantly overexpressed in RC tissue. In vitro expression of miR-21 mimic promoted the growth of 786-O cells, whereas miR-21 inhibitor inhibited cell growth by inducing apoptosis and cell cycle arrest at S phase. Furthermore, miR-21 mimic or inhibitor significantly reduced or increased the expression of PDCD4 and TPM1. Conclusions: MiR-21 is overexpressed in RC tissue and modulates the growth, apoptosis and cell cycle progression of RC cells and regulates the expression of PDCD4 and TPM1.
- 出版日期2013-6
- 单位中山大学
