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首页> 外文期刊>Central European Journal of Biology >Knockdown of DDX46 inhibits trophoblast cell proliferation and migration through the PI3K/Akt/mTOR signaling pathway in preeclampsia
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Knockdown of DDX46 inhibits trophoblast cell proliferation and migration through the PI3K/Akt/mTOR signaling pathway in preeclampsia

机译:DDX46的敲低抑制了通过PIPlampsia的PI3K / AKT / MTOR信号通路迁移的滋养细胞增殖和迁移

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摘要

Preeclampsia (PE) is a serious disease during pregnancy associated with the dysfunction of trophoblast cell invasion. DDX46 is a kind of RNA helicase that has been found to regulate cancer cell metastasis. However, the role of DDX46 in PE remains unclear. Our results showed that the mRNA levels of DDX46 in placental tissues of pregnant women with PE were markedly lower than those in normal pregnancies. Loss-of-function assays showed that knockdown of DDX46 significantly suppressed cell proliferation of trophoblast cells. Besides, DDX46 knockdown decreased trophoblast cell migration and invasion capacity. In contrast, the overexpression of DDX46 promoted the migration and invasion of trophoblast cells. Furthermore, knockdown of DDX46 caused significant decrease in the levels of p-PI3K, p-Akt, and p-mTOR in HTR-8/SVneo cells. In addition, treatment with IGF-1 reversed the inhibitory effects of DDX46 knockdown on proliferation, migration, and invasion of HTR-8/SVneo cells. In conclusion, these data suggest that DDX46 might be involved in the progression of PE, which might be attributed to the regulation of PI3K/Akt/mTOR signaling pathway. Thus, DDX46 might serve as a therapeutic target for the treatment of PE.
机译:妊娠早熟(PE)是妊娠期间的严重疾病,与滋养细胞侵袭功能障碍有关。 DDX46是一种RNA螺旋酶,已被发现调节癌细胞转移。但是,DDX46在PE中的作用仍然不清楚。我们的研究结果表明,PE孕妇胎盘组织中DDX46的mRNA水平明显低于正常怀孕的DDX46。功能丧失的测定结果显示DDX46的敲低显着抑制了滋养细胞的细胞增殖。此外,DDX46敲低滋养细胞迁移和侵袭能力降低。相反,DDX46的过表达促进了滋养细胞的迁移和侵袭。此外,DDX46的敲低导致HTR-8 / SVNEO细胞中P-PI3K,P-AKT和P-MTOR水平的显着降低。此外,用IGF-1治疗逆转DDX46敲低对HTR-8 / Svneo细胞增殖,迁移和侵袭的抑制作用。总之,这些数据表明DDX46可能涉及PE的进展,这可能归因于PI3K / AKT / MTOR信号传导路径的调节。因此,DDX46可以用作治疗PE的治疗靶标。

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