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[缺氧诱导因子-2α/Notch3信号通路介导氯化钴诱导的人乳腺癌MCF-7细胞迁移和侵袭]

[HIF-2α/Notch3 pathway mediates CoCl-induced migration and invasion in human breast cancer MCF-7 cells].

作者信息

Wang Jian-Guo, Yuan Lei

机构信息

Laboratory of Molecular Biology, Luohe Medical College, Luohe 462002, China.

出版信息

Sheng Li Xue Bao. 2016 Dec 25;68(6):783-789.

Abstract

The aim of this study is to investigate the effects of hypoxia inducible factor-2α (HIF-2α) and Notch3 on CoCl-induced migration and invasion of human breast cancer cell line MCF-7. MCF-7 cells were exposed to normoxia (21% O) or chemical hypoxia (21% O plus CoCl). Short hairpin RNA (shRNA) was used to knock down HIF-2α and Notch3 in MCF-7 cells. The mRNA expression levels of HIF-2α, Notch3 and Hey1 were measured by RT-PCR. Western blot was performed to determine the protein expression levels of HIF-2α, Notch3, Hey1, Snail and E-cadherin. CoCl treatment resulted in higher protein expression levels of HIF-2α, Notch3, Hey1, Snail (P < 0.05) and lower levels of E-cadherin (P < 0.05), and promoted migration and invasion of MCF-7 cells (P < 0.05). shRNA-HIF-2α suppressed CoCl-induced mRNA expression of Notch3 and Hey1. Notch3 knockdown down-regulated Snail and up-regulated E-cadherin at protein level under simulated hypoxia (P < 0.05), and inhibited CoCl-induced migration and invasion of MCF-7 cells (P < 0.05). In conclusion, our data provide evidence that HIF-2α may promote the migration and invasion of MCF-7 cells under chemical hypoxic conditions by potentiating Notch3 pathway.

摘要

本研究旨在探讨缺氧诱导因子-2α(HIF-2α)和Notch3对氯化钴诱导的人乳腺癌细胞系MCF-7迁移和侵袭的影响。将MCF-7细胞暴露于常氧(21% O₂)或化学缺氧(21% O₂加氯化钴)环境中。使用短发夹RNA(shRNA)敲低MCF-7细胞中的HIF-2α和Notch3。通过逆转录聚合酶链反应(RT-PCR)检测HIF-2α、Notch3和Hey1的mRNA表达水平。进行蛋白质免疫印迹法以测定HIF-2α、Notch3、Hey1、Snail和E-钙黏蛋白的蛋白质表达水平。氯化钴处理导致HIF-2α、Notch3、Hey1、Snail的蛋白质表达水平升高(P < 0.05),E-钙黏蛋白水平降低(P < 0.05),并促进了MCF-7细胞的迁移和侵袭(P < 0.05)。shRNA-HIF-2α抑制了氯化钴诱导的Notch3和Hey1的mRNA表达。在模拟缺氧条件下,敲低Notch3在蛋白质水平下调了Snail并上调了E-钙黏蛋白(P < 0.05),并抑制了氯化钴诱导的MCF-7细胞的迁移和侵袭(P < 0.05)。总之,我们的数据提供了证据表明,在化学缺氧条件下,HIF-2α可能通过增强Notch3信号通路促进MCF-7细胞的迁移和侵袭。

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