Nasreen Najmunnisa, Mohammed Kamal A, Lai Yimu, Antony Veena B
Division of Pulmonary & Critical Care Medicine, Department of Medicine, University of Florida, P.O. Box 100225, Gainesville, FL, USA.
Cancer Lett. 2007 Dec 18;258(2):215-22. doi: 10.1016/j.canlet.2007.09.005. Epub 2007 Oct 18.
The objective of this study was to understand the possible mechanisms of activation of receptor EphA2 by its ligand ephrinA1 in malignant mesothelioma cell (MMC) growth. Activation of receptor EphA2 by its ligand ephrinA1 triggered the phosphorylation of EphA2. Ligand activation of EphA2 also induced phosphorylation of ERK1/2 and significantly decreased MMC proliferation. Ligand activated and ephrinA1 vector (pcDNA/EFNA1) transfected MMC demonstrated decreased clonal growth in 3-D matrigels when compared to resting MMC. These studies suggest that EphA2 activation by its ligand ephrinA1 transmits intracellular signals from cell membrane to nucleus via ERK1/2 signaling cascade and inhibits MM growth.
本研究的目的是了解在恶性间皮瘤细胞(MMC)生长过程中,其配体ephrinA1激活受体EphA2的可能机制。其配体ephrinA1激活受体EphA2会引发EphA2的磷酸化。EphA2的配体激活还会诱导ERK1/2的磷酸化,并显著降低MMC的增殖。与静止的MMC相比,配体激活的和转染了ephrinA1载体(pcDNA/EFNA1)的MMC在三维基质胶中显示出克隆生长减少。这些研究表明,其配体ephrinA1激活EphA2可通过ERK1/2信号级联将细胞内信号从细胞膜传递至细胞核,并抑制MM生长。