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The Roles of Mitogen-Activated Protein Kinase Pathways in TGF-β-Induced Epithelial-Mesenchymal Transition

机译:丝裂原激活的蛋白激酶途径在TGF-β诱导的上皮-间质转化中的作用

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摘要

The mitogen-activated protein kinase (MAPK) pathway allows cells to interpret external signals and respond appropriately, especially during the epithelial-mesenchymal transition (EMT). EMT is an important process during embryonic development, fibrosis, and tumor progression in which epithelial cells acquire mesenchymal, fibroblast-like properties and show reduced intercellular adhesion and increased motility. TGF-β signaling is the first pathway to be described as an inducer of EMT, and its relationship with the Smad family is already well characterized. Studies of four members of the MAPK family in different biological systems have shown that the MAPK and TGF-β signaling pathways interact with each other and have a synergistic effect on the secretion of additional growth factors and cytokines that in turn promote EMT. In this paper, we present background on the regulation and function of MAPKs and their cascades, highlight the mechanisms of MAPK crosstalk with TGF-β signaling, and discuss the roles of MAPKs in EMT.
机译:丝裂原激活的蛋白激酶(MAPK)途径使细胞能够解释外部信号并做出适当的反应,特别是在上皮-间质转化(EMT)期间。 EMT是胚胎发育,纤维化和肿瘤发展过程中的重要过程,在该过程中,上皮细胞具有间充质,成纤维细胞样特性,并表现出减少的细胞间粘附和运动性。 TGF-β信号传导是被描述为EMT诱导剂的第一个途径,其与Smad家族的关系已经得到很好的表征。对不同生物学系统中MAPK家族的四个成员的研究表明,MAPK和TGF-β信号传导途径彼此相互作用,并且对其他生长因子和细胞因子的分泌具有协同作用,从而促进了EMT。在本文中,我们介绍了MAPK及其级联的调控和功能的背景,突出了MAPK与TGF-β信号传导的串扰机制,并讨论了MAPK在EMT中的作用。

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