Savagner P
Equipe Genome et Cancer, UMR CNRS 5535, CRLC Val d'Aurelle-Paul Larmarque, 34298 Montpellier, cedex 5, France.
Bioessays. 2001 Oct;23(10):912-23. doi: 10.1002/bies.1132.
Several molecular mechanisms contribute directly and mechanically to the loss of epithelial phenotype. During epithelial-mesenchymal transition (EMT), adherens junctions and desmosomes are at least partially dissociated. At the same time, a massive cytoskeleton reorganization takes place, involving the rho family and the remodeling of the actin microfilament mesh. Numerous pathways have been described in vitro that control phenotype transition in specific cell models. In vivo developmental studies suggest that transcriptional control, activated by a specific pathway involving Ras, Src and potentially the Wnt pathway, is an essential step. Recent functional and localization experiments indicate that the slug/snail family of transcription factors functions overall as an epithelial phenotype repressor and could represent a key EMT contributor.
几种分子机制直接且机械地导致上皮表型丧失。在上皮-间质转化(EMT)过程中,黏着连接和桥粒至少部分解离。与此同时,发生大规模的细胞骨架重组,涉及Rho家族和肌动蛋白微丝网络的重塑。在体外已经描述了许多控制特定细胞模型中表型转变的途径。体内发育研究表明,由涉及Ras、Src以及可能的Wnt途径的特定途径激活的转录控制是一个关键步骤。最近的功能和定位实验表明,转录因子的Slug/Snail家族总体上作为上皮表型的抑制因子发挥作用,可能是EMT的关键促成因素。