首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >Benzo[a]Pyrene-7, 8-Diol-9, 10-Epoxide Suppresses the Migration and Invasion of Human Extravillous Trophoblast Swan 71 Cells Due to the Inhibited Filopodia Formation and Down-Regulated PI3K/AKT/CDC42/PAK1 Pathway Mediated by the Increased miR-194-3p
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Benzo[a]Pyrene-7, 8-Diol-9, 10-Epoxide Suppresses the Migration and Invasion of Human Extravillous Trophoblast Swan 71 Cells Due to the Inhibited Filopodia Formation and Down-Regulated PI3K/AKT/CDC42/PAK1 Pathway Mediated by the Increased miR-194-3p

机译:苯并[a]芘-7,8-二醇-9,10-环氧化抑制了人外向性滋养流血管滋养细胞SWAN 71细胞的迁移和侵袭由于抑制的箔片形成和下调的PI3K / AKT / CDC42 / PAK1途径 mir-194-3p增加

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摘要

Proper migration and invasion of trophoblast cells into endometrium is vital for successful embryo implantation during early pregnancy. Benzo[a]pyrene-7, 8-diol-9, 10-epoxide (BPDE) is an ultimate carcinogenic product of benzo[a]pyrene (BaP), which causes multiple trophoblast-related diseases. However, the mechanism of BPDE-inhibited migration/invasion of trophoblast cells is still unclear. In this work, we found that BPDE significantly inhibited the filopodia formation and migration/invasion of human trophoblast Swan 71 cells. BPDE up-regulated the level of miR-194-3p, which further inhibited the phosphoinositide 3-kinase (PI3K)/AKT/ cell division cycle 42/ p21 (RAC1) activated kinase 1 signaling pathway and depressed the filophdia formation of Swan71 cells. Addition of 740 Y-P, the activator of phosphoinositide 3-kinase, could stimulate cell migration/invasion, confirming the involvement of this pathway. Knock-down of miR-194-3p up-regulated this pathway and promoted filopodia formation and migration/invasion. Conversely, overexpression of miR-194-3p down-regulated this pathway and inhibited cell migration/invasion. Therefore, miR-194-3p takes important roles in the BPDE-inhibited filopodia formation and cell migration/invasion, providing valuable information in the BPDE-induced dysfunctions of human extravillous trophoblast cells.
机译:适当的迁移和孕产细胞进入子宫内膜的侵袭对于在妊娠期间成功胚胎植入至关重要。苯并[a]芘-7,8-二醇-9,10-环氧化(BPDE)是苯并[a]芘(BAP)的最终致癌产物,其导致多种滋养管相关疾病。然而,BPDE抑制迁移/侵袭的机制仍不清楚。在这项工作中,我们发现BPDE显着抑制了人滋养细胞SWAN 71细胞的氟膜形成和迁移/侵袭。 BPDE上调miR-194-3p的水平,进一步抑制磷酸阳性3-激酶(Pi3k)/ akt /细胞分裂循环42 / p21(Rac1)活化激酶1信号传导途径,并抑制了Swan71细胞的丝细胞形成。添加740 y-p,磷酸膦酸的活化剂3-激酶,可以刺激细胞迁移/侵袭,证实该途径的累及。 MIR-194-3P的击倒上调该途径和促进了剥离覆盖层和移民/入侵。相反,MIR-194-3P的过度表达下调该途径并抑制细胞迁移/侵袭。因此,MIR-194-3P在BPDE抑制的氟膜形成和细胞迁移/侵袭中具有重要作用,提供了BPDE诱导的人外向性滋养细胞的功能障碍中的有价值的信息。

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