miR-150, p53 protein and relevant miRNAs consist of a regulatory network in NSCLC tumorigenesis | |
Wang, DT; Ma, ZL; Li, YL; Wang, YQ; Zhao, BT; Wei, JL; Qiu, X; Zhao, XT; Jin, YX | |
刊名 | ONCOLOGY REPORTS |
2013 | |
卷号 | 30期号:1页码:492-498 |
关键词 | miR-150 p53 protein miRNA NSCLC |
通讯作者 | Ma, ZL (reprint author), Shanghai Univ, Sch Life Sci, 99 Shangda Rd, Shanghai 200444, Peoples R China.,zlma@shu.edu.cn ; yxjin@sibs.ac.cn |
英文摘要 | microRNAs (miRNAs) are a class of non-coding small RNAs that act as negative regulators of gene expression by binding to the 3'-untranslated region (3'-UTR) of target mRNAs. Tumor protein p53, a transcriptional factor, plays an important role in the progression of tumorigenesis. miR-150 was the only miRNA predicted to target 3'-UTR of p53 by TargetScan. In order to investigate the function of miR-150, p53 and relevant miRNAs in non-small cell lung cancer (NSCLC), we constructed two expression vectors of p53 (pcDNA3.1-p53 and pcDNA3.1-p53-3'-UTR) and two report vectors (pGL3-p53-3'-UTR and pGL3-p53-3'-mUTR). The activity of luciferase transfected with miR-150 mimics was lower by 30% when compared to that of the miRNA-negative control (miRNA-NC). Moreover, the p53 protein was downregulated by at least 50% when miR-150 mimics were cotransfected with pcDNA3.1-p53-3'-UTR when compared to miRNA-NC. We also determined the expression of miR-150 and p53 in NSCLC patient tissue samples. The expression of miR-150 in T2 stage tissue samples was higher than that in T1 stage tissue samples. The corresponding target gene p53 was correlated with miR-150 expression. In the present study, we further analyzed the cell cycle distribution. The cells transfected with pcDNA3.1-p53 were significantly arrested in the G1 phase when compared to the control cells. When miR-150 mimics were cotransfected with pcDNA3.1-p53-3'-UTR, the percentage of cells in the G1 phase was significantly lower by 4% when compared to miRNA-NC. To identify miRNAs that are regulated by the p53 protein, qRT-PCR was performed after pcDNA3.1-p53 transfection. miR-34a, miR-184, miR-181a and miR-148 were upregulated significantly. However, there was no distinct difference in the expression of miR-10a, miR-182 and miR-34c. Our results showed that miR-150 targets the 3'-UTR of p53, and p53 protein promotes the expression of miRNAs which affect cell cycle progression. These findings suggest that miR-150, p53 protein and relevant miRNAs are members of a regulatory network in NSCLC tumorigenesis. |
学科主题 | Oncology |
类目[WOS] | Oncology |
关键词[WOS] | TARGETING NOTCH1 ; CANCER CELLS ; EXPRESSION ; PATHWAY ; MIR-34A ; PROLIFERATION ; MICRORNA-34A ; CARCINOMA ; APOPTOSIS |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000321077500069 |
内容类型 | 期刊论文 |
版本 | 出版稿 |
源URL | [http://202.127.25.143/handle/331003/312] |
专题 | 上海生化细胞研究所_上海生科院生化细胞研究所 |
推荐引用方式 GB/T 7714 | Wang, DT,Ma, ZL,Li, YL,et al. miR-150, p53 protein and relevant miRNAs consist of a regulatory network in NSCLC tumorigenesis[J]. ONCOLOGY REPORTS,2013,30(1):492-498. |
APA | Wang, DT.,Ma, ZL.,Li, YL.,Wang, YQ.,Zhao, BT.,...&Jin, YX.(2013).miR-150, p53 protein and relevant miRNAs consist of a regulatory network in NSCLC tumorigenesis.ONCOLOGY REPORTS,30(1),492-498. |
MLA | Wang, DT,et al."miR-150, p53 protein and relevant miRNAs consist of a regulatory network in NSCLC tumorigenesis".ONCOLOGY REPORTS 30.1(2013):492-498. |
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