Schlegel Natalie C, von Planta Anina, Widmer Daniel S, Dummer Reinhard, Christofori Gerhard
Department of Biomedicine, University of Basel, Basel, Switzerland.
Exp Dermatol. 2015 Jan;24(1):22-8. doi: 10.1111/exd.12580. Epub 2014 Nov 18.
Epithelial to mesenchymal transition (EMT) is a programme defined in epithelial cells and recognized as playing a critical role in cancer progression. Although melanoma is not a cancer of epithelial cells, hallmarks of EMT have been described to play a critical role in melanoma progression. Here, we demonstrate that long-term TGFβ exposure can induce a dedifferentiated EMT-like state resembling a previously described invasive phenotype (EMT-like). TGFβ-induced EMT-like is marked by the downregulation of melanocyte differentiation markers, such as MITF, and the upregulation of mesenchymal markers, such as N-cadherin, and an increase in melanoma cell migration and cell invasion. Pharmacological interference shows the dependency of TGFβ-induced EMT-like on the activation of the PDGF signalling pathway and the subsequent activation of PI3K in human melanoma cells. Together, the data provide novel insights into the transcriptional plasticity of melanoma cells that might contribute to tumor progression in patients and propose avenues to therapeutic interventions.
上皮-间质转化(EMT)是一种在上皮细胞中定义的程序,被认为在癌症进展中起关键作用。尽管黑色素瘤不是上皮细胞癌,但已有研究表明EMT的特征在黑色素瘤进展中起关键作用。在此,我们证明长期暴露于转化生长因子β(TGFβ)可诱导一种去分化的类似EMT的状态,类似于先前描述的侵袭性表型(EMT样)。TGFβ诱导的EMT样表现为黑素细胞分化标志物(如小眼畸形相关转录因子,MITF)的下调,间充质标志物(如N-钙黏蛋白)的上调,以及黑色素瘤细胞迁移和侵袭的增加。药理学干预表明,TGFβ诱导的EMT样依赖于血小板衍生生长因子(PDGF)信号通路的激活以及随后人黑色素瘤细胞中磷脂酰肌醇-3-激酶(PI3K)的激活。这些数据共同为黑色素瘤细胞的转录可塑性提供了新的见解,这可能有助于患者的肿瘤进展,并为治疗干预提出了途径。