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首页> 外文期刊>Biochemical and Biophysical Research Communications >Hypoxia induces RANK and RANKL expression by activating HIF-1alpha in breast cancer cells.
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Hypoxia induces RANK and RANKL expression by activating HIF-1alpha in breast cancer cells.

机译:低氧通过激活乳腺癌细胞中的HIF-1alpha诱导RANK和RANKL表达。

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Receptor activator of NF-kappaB (RANK) and RANK ligand (RANKL) are known to play an important role in the development and progression of breast cancer. However, the mechanisms by which stimuli regulate the expression of RANK and RANKL in breast cancer cells are largely unknown. In this study, we show that hypoxia, a common feature of malignant tumors, can enhance the expression of RANK and RANKL mRNA and protein in MDA-MB-231 and MCF-7 breast cancer cells. In addition, we found that hypoxia induced hypoxia-inducible factor-1 alpha (HIF-1alpha) and phosphorylation of Akt, resulting in upregulation of RANK and RANKL expression; HIF-1alpha-targeted siRNA and PI3K-Akt inhibitor abrogated this upregulation in MDA-MB-231 cells. Furthermore, we also observed that hypoxia accelerated RANKL-mediated cell migration, which was inhibited following HIF-1alpha knockdown and PI3K-Akt inhibition. Thus, we provide evidence that hypoxia upregulates RANK and RANKL expression and increases RANKL-induced cell migration via the PI3K/Akt-HIF-1alpha pathway.
机译:已知NF-κB(RANK)和RANK配体(RANKL)的受体激活剂在乳腺癌的发生和发展中起着重要的作用。然而,刺激调节乳腺癌细胞中RANK和RANKL表达的机制在很大程度上是未知的。在这项研究中,我们表明缺氧是恶性肿瘤的常见特征,可以增强MDA-MB-231和MCF-7乳腺癌细胞中RANK和RANKL mRNA和蛋白的表达。此外,我们发现缺氧诱导缺氧诱导因子-1α(HIF-1alpha)和Akt磷酸化,导致RANK和RANKL表达上调; HIF-1alpha靶向的siRNA和PI3K-Akt抑制剂消除了MDA-MB-231细胞中的这种上调。此外,我们还观察到,缺氧会加速RANKL介导的细胞迁移,这在HIF-1alpha敲低和PI3K-Akt抑制后被抑制。因此,我们提供证据表明缺氧通过PI3K / Akt-HIF-1alpha途径上调RANK和RANKL表达并增加RANKL诱导的细胞迁移。

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