| Literature DB >> 30841423 |
Huimin Wang1, Zhongliang Ma1, Xiaomin Liu1, Caiyan Zhang1, Yanping Hu2, Lei Ding1, Pengfei Qi1, Ju Wang3, Shengdi Lu4, Yanli Li5.
Abstract
Lung cancer is the leading cause in all cancer deaths. A low survival rate and high recurrence rate of lung cancer make the endeavor to identify new, more effective therapies a primary goal. MicroRNAs (miRNAs) are regarded as regulators of tumorigenesis and it is known that miR-183-5p is significantly upregulated in non-small cell lung cancer (NSCLC), suggesting it has an oncogenic function in lung cancer. In this study, we found that miR-183-5p could promote lung carcinogenesis by directly targeting phosphatase tensin (PTEN). Further experiments indicated that miR-183-5p could suppress p53 and activate AKT signaling through phosphorylation. Moreover, our data indicated that miR-183-5p promoted tumor metastasis and tumor growth in vivo. Collectively, these results showed that miR-183-5p is required for NSCLC development through the suppressing PTEN, and might be a promising target in the diagnosis and treatment of lung cancer in the future.Entities:
Keywords: Non-small cell lung cancer; PTEN; Tumorigenesis; miR-183-5p
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Year: 2019 PMID: 30841423 DOI: 10.1016/j.biopha.2018.12.115
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529