| Literature DB >> 30679790 |
Manale El Kharbili1,2,3,4, Gweltaz Agaësse1,2,3, Laetitia Barbollat-Boutrand1,2,3,5, Roxane M Pommier5, Arnaud de la Fouchardière5,6, Lionel Larue7,8,9, Julie Caramel5, Alain Puisieux5, Odile Berthier-Vergnes1,2,3, Ingrid Masse10,11,12,13.
Abstract
Due to its high proclivity to metastasize, and despite the recent development of targeted and immune therapy strategies, melanoma is still the deadliest form of skin cancer. Therefore, understanding the molecular mechanisms underlying melanoma invasion remains crucial. We previously characterized Tspan8 for its ability to prompt melanoma cell detachment from their microenvironment and trigger melanoma cell invasiveness, but the signaling events by which Tspan8 regulates the invasion process still remain unknown. Here, we demonstrated that β-catenin stabilization is a molecular signal subsequent to the onset of Tspan8 expression, and that, in turn, β-catenin triggers the direct transcriptional activation of Tspan8 expression, leading to melanoma invasion. Moreover, we showed that β-catenin activation systematically correlates with a high expression of Tspan8 protein in melanoma lesions from transgenic Nras; bcat* mice, as well as in deep penetrating naevi, a type of human pre-melanoma neoplasm characterized by a combined activation of β-catenin and MAP kinase signaling. Overall, our data suggest that β-catenin and Tspan8 are part of a positive feedback loop, which sustains a high Tspan8 expression level, conferring to melanoma cells the invasive properties required for tumor progression and dissemination.Entities:
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Year: 2019 PMID: 30679790 DOI: 10.1038/s41388-019-0691-z
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867