作者: Alejandro Conde-Perez , Gwendoline Gros , Christine Longvert , Malin Pedersen , Valérie Petit
DOI: 10.1038/NCOMMS9093
关键词: Catenin 、 Caveolin 1 、 PI3K/AKT/mTOR pathway 、 Protein kinase B 、 Cell biology 、 GSK-3 、 Biology 、 Internalization 、 Beta-catenin 、 Cancer research 、 PTEN
摘要: Loss of the tumour suppressor PTEN is frequent in human melanoma, results MAPK activation, suppresses senescence and mediates metastatic behaviour. How loss these effects unknown. Here we show that epithelial melanocytic cell lines induces nuclear localization transcriptional activation β-catenin independent PI3K-AKT-GSK3β axis. The absence leads to caveolin-1 (CAV1)-dependent modulation vitro, cooperates with NRAS(Q61K) initiate melanomagenesis vivo efficient metastasis formation associated E-cadherin internalization. CAV1-β-catenin axis mediated by a feedback loop which represses transcription miR-199a-5p miR-203, suppress levels CAV1 mRNA melanoma cells. These data reveal mechanism increases CAV1-mediated dissociation from membranous E-cadherin, may promote bypass metastasis.