MicroRNA-198-5p inhibits the migration and invasion of non-small lung cancer cells by targeting fucosyltransferase 8

被引:31
作者
Wang, Siyao [1 ]
Zhang, Xin [1 ]
Yang, Chunlu [1 ]
Xu, Shun [1 ]
机构
[1] China Med Univ, Hosp 1, Dept Thorac Surg, Shenyang 110001, Liaoning, Peoples R China
关键词
epithelial-to-mesenchymal transition; fucosyltransferase; 8; invasion; microRNA-198-5p; migration; non-small cell lung cancer; EXPRESSION; MIR-198; PROLIFERATION; GLYCOSYLATION; METASTASIS; FUT8;
D O I
10.1111/1440-1681.13154
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MicroRNA-198-5p (miR-198-5p) displays crucial roles in various cancers including non-small cell lung cancer (NSCLC), but the underlying molecular mechanisms remain unclear. Fucosyltransferase 8 (FUT8) is associated with tumour metastasis and prognosis. In this study, we explored the expression of miR-198-5p and FUT8 in NSCLC patients. Results showed that miR-198-5p was under-expressed in NSCLC tissues and was negatively correlated with tumour size, lymph node metastasis and tumour-node-metastasis stage, while FUT8 expression was highly upregulated. Next, we altered miR-198-5p expression using the mimic or inhibitor in the functional study. Results showed that miR-198-5p overexpression could inhibit the migration, invasion and epithelial-to-mesenchymal transition (EMT) of NSCLC cells; reversely, suppression of miR-198-5p enhanced cell migration, invasion and EMT. In vivo, miR-198-5p overexpression inhibited the formation of mouse lung and liver metastasis. Luciferase reporter, real-time PCR and western blot assays showed that miR-198-5p could directly target FUT8 and regulate FUT8 expression. Further, FUT8 overexpression reversed the effect of miR-198-5p overexpression on the migration, invasion and EMT of NSCLC cells. Taken together, miR-198-5p functions as a tumour suppressor by targeting FUT8 in NSCLC. MiR-198-5p may be developed as a new diagnostic biomarker and therapeutic target for lung cancer.
引用
收藏
页码:955 / 967
页数:13
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