Eur Rev Med Pharmacol Sci 2018; 22 (4): 961-969

DOI: 10.26355/eurrev_201802_14377

Up-regulation of miR-190b promoted growth, invasion, migration and inhibited apoptosis of Wilms’ tumor cells by repressing the PTEN expression

N.-N. An, J. Shawn, J.-P. Peng, M.-D. Wu, L.-G. Huang

West China School of Medicine, Sichuan University, Chengdu, China. Lugang992001@aliyun.com


OBJECTIVE: Wilms’ tumor (WT) is the most common malignant tumor in the children’s urogenital system. MiR-190b was found to participate in the development and progression of several cancers. However, the molecular mechanism of miR-190b in WT is still unclear.

PATIENTS AND METHODS: We detected the miR-190b in WT tissue samples compared to adjacent normal samples as well as in WT patients’ blood sample compared to normal volunteers using qRT-PCR. With over-expression and knockdown of miR-190b in WT-derived cell line SK-NEP-1, we next studied cell proliferation, cell circle, apoptosis, invasion and migration abilities change caused by miR-190b ectopic expression. Dual-luciferase assay and Western-blot analysis were used to explain the mechanism of miR-190b in WT.

RESULTS: MiR-190b was over-expressed in WT tissue and blood samples compared to normal group, relatively. Up-regulation of miR-190b in SK-NEP-1 cells significantly increased the growth and decreased the apoptosis of cells, while its down-regulation reduced cell proliferation and promoted cell apoptosis of SK-NEP-1. Also, cell invasion and migration abilities were significantly improved after miR-190b over-expression. Moreover, PTEN was proved to be a direct target of miR-190b and its protein level was remarkably decreased after miR-190b up-regulation.

CONCLUSIONS: miR-190b over-expressed in WT and promoted cell proliferation, invasion and migration while reduced cell apoptosis of WT cells by repressing PTEN repression, which might provide a potential target for WT diagnosis and therapy.

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To cite this article

N.-N. An, J. Shawn, J.-P. Peng, M.-D. Wu, L.-G. Huang
Up-regulation of miR-190b promoted growth, invasion, migration and inhibited apoptosis of Wilms’ tumor cells by repressing the PTEN expression

Eur Rev Med Pharmacol Sci
Year: 2018
Vol. 22 - N. 4
Pages: 961-969
DOI: 10.26355/eurrev_201802_14377