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Downregulation of miR-493 promoted melanoma proliferation by suppressing IRS4 expression
Author(s) -
Aili Cui,
Zhehu Jin,
Zhonggao Gao,
Mingji Jin,
Lianhua Zhu,
Lianhua Li,
Chenglong Jin,
Yinghua An
Publication year - 2017
Publication title -
tumor biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 84
eISSN - 1423-0380
pISSN - 1010-4283
DOI - 10.1177/1010428317701640
Subject(s) - downregulation and upregulation , cell growth , gene knockdown , microrna , melanoma , cancer research , cell cycle , cell culture , luciferase , biology , cell , microbiology and biotechnology , transfection , gene , genetics
Accumulating evidence indicated that aberrantly expressed microRNAs play critical roles in the initiation and progression of human cancers. However, the underlying functions of miR-493 in human melanoma remains unknown. Here, our study found that miR-493 expression was downregulated in human melanoma tissues and cells. Overexpression of miR-493 suppressed cell proliferation and cell cycle in human melanoma cell line A375. IRS4 was defined as a target for downregulation by miR-493 and was confirmed by luciferase assay. We also found that knockdown of IRS4 counteracted the proliferation promotion by miR-493 inhibitor. In summary, these results demonstrated that miR-493 acts as a tumor suppressor and inhibits cell proliferation and cell cycle in human melanoma by directly targeting IRS4.

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