Larue Lionel, Bellacosa Alfonso
Developmental Genetics of Melanocytes, UMR 146, CNRS, Institut Curie, Centre Universitaire, Orsay, France.
Oncogene. 2005 Nov 14;24(50):7443-54. doi: 10.1038/sj.onc.1209091.
Epithelial-mesenchymal transition (EMT) is an important process during development by which epithelial cells acquire mesenchymal, fibroblast-like properties and show reduced intercellular adhesion and increased motility. Accumulating evidence points to a critical role of EMT-like events during tumor progression and malignant transformation, endowing the incipient cancer cell with invasive and metastatic properties. Several oncogenic pathways (peptide growth factors, Src, Ras, Ets, integrin, Wnt/beta-catenin and Notch) induce EMT and a critical molecular event is the downregulation of the cell adhesion molecule E-cadherin. Recently, activation of the phosphatidylinositol 3' kinase (PI3K)/AKT axis is emerging as a central feature of EMT. In this review, we discuss the role of PI3K/AKT pathways in EMT during development and cancer with a focus on E-cadherin regulation. Interactions between PI3K/AKT and other EMT-inducing pathways are presented, along with a discussion of the therapeutic implications of modulating EMT in order to achieve cancer control.
上皮-间质转化(EMT)是发育过程中的一个重要过程,通过该过程上皮细胞获得间质、成纤维细胞样特性,并表现出细胞间粘附减少和运动性增加。越来越多的证据表明,类似EMT的事件在肿瘤进展和恶性转化过程中起关键作用,赋予初始癌细胞侵袭和转移特性。几种致癌途径(肽生长因子、Src、Ras、Ets、整合素、Wnt/β-连环蛋白和Notch)诱导EMT,一个关键的分子事件是细胞粘附分子E-钙粘蛋白的下调。最近,磷脂酰肌醇3'激酶(PI3K)/AKT轴的激活正成为EMT的一个核心特征。在本综述中,我们讨论了PI3K/AKT途径在发育和癌症过程中EMT中的作用,重点是E-钙粘蛋白的调节。介绍了PI3K/AKT与其他诱导EMT途径之间的相互作用,并讨论了调节EMT以实现癌症控制的治疗意义。