| Literature DB >> 29935356 |
Yingzhi Qin1, Xiaoyun Zhou1, Cheng Huang1, Li Li1, Hongsheng Liu2, Naixin Liang1, Yeye Chen1, Dongjie Ma1, Zhijun Han1, Xiaohui Xu1, Jia He1, Shanqing Li1.
Abstract
Aberrantly microRNAs (miRs) expression is reported to be involved in tumorigenesis and development in non-small cell lung cancer (NSCLC). MiR-340 had been identified to be downregulated in NSCLC in the previous study. However, the underlying mechanisms of miR-340 involved in NSCLC progression still needed to be well known. In the present study, we confirmed that miR-340 expression was notably down-regulated in NSCLC tissues compared to matched adjacent noncancerous lung tissues by quantitative real time PCR (qRT-PCR) analyses. Lower miR-340 expression positively related to lymph node metastasis, larger tumor size, advanced TNM stage and poor prognosis of NSCLC patients. In vitro assays, we demonstrated that upregulation of miR-340 expression suppressed cell proliferation ability. Bioinformatics analysis and luciferase reporter assays revealed that miR-340 directly targeted the 3'-untranslated (3'UTR) region of CDK4 mRNA. Over-expression of miR-340 suppressed cell proliferation by regulating CDK4 expression in NSCLC cells. Additionally, we showed that increased miR-340 expression promoted the expression of cell proliferation related protein CDK6 expression, but decreasing the P15 and P21 expression. In vivo, we verified that miR-340 overexpression also inhibited tumor growth by regulating CDK4 expression. Therefore, these findings revealed miR-340 functions as a tumor suppressor in NSCLC cells and may provide a potential target of NSCLC treatment.Entities:
Keywords: CDK4; Cell proliferation; MircroRNA; Non-small cell lung cancer; miR-340
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Year: 2018 PMID: 29935356 DOI: 10.1016/j.gene.2018.06.062
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688