miRNA-584-3p inhibits gastric cancer progression by repressing Yin Yang 1- facilitated MMP-14 expression
Recent evidence shows the emerging roles of promoter-targeting endogenous microRNAs (miRNAs) in regulating gene transcription. However, miRNAs affecting the transcription of matrix metalloproteinase 14 ( MMP-14 ) in gastric cancer remain unknown. Herein, through integrative mining of public datasets...
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Veröffentlicht in: | Scientific reports 2017-08, Vol.7 (1), p.8967-14, Article 8967 |
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Sprache: | eng |
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Zusammenfassung: | Recent evidence shows the emerging roles of promoter-targeting endogenous microRNAs (miRNAs) in regulating gene transcription. However, miRNAs affecting the transcription of matrix metalloproteinase 14 (
MMP-14
) in gastric cancer remain unknown. Herein, through integrative mining of public datasets, we identified the adjacent targeting sites of Yin Yang 1 (YY1) and miRNA-584-3p (miR-584-3p) within
MMP-14
promoter. We demonstrated that YY1 directly targeted the
MMP-14
promoter to facilitate its expression in gastric cancer cells. In contrast, miR-584-3p recognized its complementary site within
MMP-14
promoter to suppress its expression. Mechanistically, miR-584-3p interacted with Argonaute 2 to recruit enhancer of zeste homolog 2 and euchromatic histone lysine methyltransferase 2, resulting in enrichment of repressive epigenetic markers and decreased binding of YY1 to
MMP-14
promoter. miR-584-3p inhibited the
in vitro
and
in vivo
tumorigenesis and aggressiveness of gastric cancer cells through repressing YY1-facilitated MMP-14 expression. In clinical gastric cancer tissues, the expression of YY1 and miR-584-3p was positively or negatively correlated with MMP-14 levels. In addition, miR-584-3p and YY1 were independent prognostic factors associated with favorable and unfavorable outcome of gastric cancer patients, respectively. These data demonstrate that miR-584-3p directly targets the
MMP-14
promoter to repress YY1-facilitated MMP-14 expression and inhibits the progression of gastric cancer. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-017-09271-5 |