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EGFR: A Master Piece in G1/S Phase Transition of Liver Regeneration

机译:EGFR:肝再生G1 / S相变的杰作

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Unraveling the molecular clues of liver proliferation has become conceivable thanks to the model of two-third hepatectomy. The synchronicity and the well-scheduled aspect of this process allow scientists to slowly decipher this mystery. During this phenomenon, quiescent hepatocytes of the remnant lobes are able to reenter into the cell cycle initiating the G1-S progression synchronously before completing the cell cycle. The major role played by this step of the cell cycle has been emphasized by loss-of-function studies showing a delay or a lack of coordination in the hepatocytes G1-S progression. Two growth factor receptors, c-Met and EGFR, tightly drive this transition. Due to the level of complexity surrounding EGFR signaling, involving numerous ligands, highly controlled regulations and multiple downstream pathways, we chose to focus on the EGFR pathway for this paper. We will first describe the EGFR pathway in its integrity and then address its essential role in the G1/S phase transition for hepatocyte proliferation. Recently, other levels of control have been discovered to monitor this pathway, which will lead us to discuss regulations of the EGFR pathway and highlight the potential effect of misregulations in pathologies.
机译:由于三分之二肝切除术的模型,弄清了肝增殖的分子线索已经成为可能。这个过程的同步性和精心安排的方面使科学家能够慢慢地解开这个谜团。在此现象期间,剩余叶的静止肝细胞能够重新进入细胞周期,从而在完成细胞周期之前同步启动G1-S进程。功能丧失研究强调了细胞周期这一步骤所起的主要作用,研究显示肝细胞G1-S进程延迟或缺乏协调。两种生长因子受体c-Met和EGFR紧密驱动这一转变。由于围绕EGFR信号传导的复杂性水平,涉及众多配体,高度受控的法规和多个下游途径,因此本文选择聚焦于EGFR途径。我们将首先描述其完整性的EGFR途径,然后讨论其在肝细胞增殖的G1 / S相变中的重要作用。最近,发现了其他水平的监控该途径的监测方法,这将使我们讨论EGFR途径的调控并突出病理学失调的潜在影响。

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