Literature DB >> 30542503

MicroRNA-598 inhibits the proliferation and invasion of non-small cell lung cancer cells by directly targeting ZEB2.

Xiangdong Tong1, Peng Su2, Haitao Yang1, Fusheng Chi1, Lin Shen1, Xiao Feng1, Hongqian Jiang1, Xiuchun Zhang1, Zhenyuan Wang1.   

Abstract

An increasing number of studies have observed that microRNAs (miRNAs) are abnormally expressed in non-small cell lung cancer (NSCLC), and that their aberrant expression links with the progression and development of NSCLC. Therefore, it is necessary to full elucidate the specific roles of miRNAs in NSCLC, as this may facilitate the identification of novel therapeutic targets. In the present study, it was observed that miRNA-598 (miR-598) expression was significantly downregulated in NSCLC tissues and cell lines. Decreased miR-598 was negatively correlated with TNM stage and lymph node metastasis in NSCLC patients. In addition, ectopic expression of miR-598 reduced NSCLC cell proliferation and invasion in vitro. The zinc finger E-box-binding homeobox 2 (ZEB2) was validated as a direct target of miR-598 in NSCLC cells. ZEB2 was upregulated in NSCLC tissues and the upregulation of ZEB2 was inversely correlated with the miR-598 level. The results revealed that restored ZEB2 expression abrogated the inhibitory effects of miR-598 overexpression in NSCLC cells. In conclusion, the results of the present study revealed that miR-598 may inhibit the progression of NSCLC by directly targeting ZEB2, which suggests that this miRNA may be identified as a potential novel prognostic biomarker and therapeutic target for patients with NSCLC.

Entities:  

Keywords:  invasion; microRNA-598; non-small cell lung cancer; proliferation; zinc finger E-box-binding homeobox 2

Year:  2018        PMID: 30542503      PMCID: PMC6257717          DOI: 10.3892/etm.2018.6825

Source DB:  PubMed          Journal:  Exp Ther Med        ISSN: 1792-0981            Impact factor:   2.751


  42 in total

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Review 9.  Epigenetics and MicroRNAs in Cancer.

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6.  MicroRNA-598 inhibits the growth of triple negative breast cancer cells by targeting JAG1.

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