期刊论文详细信息
Bioengineered
MiR-212-3p promotes proliferation and migration of trophoblast in fetal growth restriction by targeting placental growth factor
Limin Yu1  Yan Sun1  Zanjun Chu1 
[1] Department of Gynecology and Obstetrics, Tianjin Medical University General Hospital, Tianjin, Chin;Tianjin Key Layboratory of Female Reproductive Health and Eugenics, Tianjin, Chin;
关键词: Fetal growth restriction;    miR-212-3p;    PGF;    PI3K/AKT signaling pathway;    biomarkers;   
DOI  :  10.1080/21655979.2021.1967069
来源: Taylor & Francis
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【 摘 要 】

The purpose of this study was to evaluate the function and possible mechanism of miR-212-3p in fetal growth restriction (FGR) and to demonstrate the relationship between miR-212-3p and placental growth factor (PGF). First, we used qRT-PCR to detect the expression of miR-212-3p and PGF in placental tissues of normal delivery (HC group) and FGR, as well as in human trophoblast cell HTR-8/Svneo. The results revealed that miR-212-3p expression was significantly upregulated and PGF was significantly downregulated in placental tissue in the FGR group compared with the HC group. In addition, interference with miR-212-3p expression increased the proliferation, invasion, and migration of HTR-8/SVneo cells and decreased apoptosis of cells. Meanwhile, Western blot results showed that miR-212-3p expression downregulation promoted the phosphorylated protein expression of Phosphoinositide 3-kinase (PI3K) and protein kinase B (AKT), which in turn activated the PI3K/AKT signaling pathway. And the results of dual luciferase reporter further showed that miR-212-3p could target PGF, and the expression of both was negatively correlated in FGR group tissues. In addition, downregulation of miR-212-3p expression reversed the inhibitory effect of PGF downregulation on HTR-8/SVneo cells. In conclusion, miR-212-3p can target and inhibit the PGF expression and regulate the PI3K/AKT signaling pathway to regulate trophoblast cell invasion, migration, proliferation and cell apoptosis. This provides a potential biomarker for the development of FGR.

【 授权许可】

CC BY   

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