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Supplementary Methods and References from Snail1-Dependent Activation of Cancer-Associated Fibroblast Controls Epithelial Tumor Cell Invasion and Metastasis

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posted on 2023-03-31, 00:23 authored by Lorena Alba-Castellón, Rubén Olivera-Salguero, Aida Mestre-Farrera, Raúl Peña, Mercedes Herrera, Félix Bonilla, J. Ignacio Casal, Josep Baulida, Cristina Peña, Antonio García de Herreros

Description of additional methods and procedures used in the study. Also includes Supplementary References.

Funding

Fundación Científica de la Asociación Española contra el Cáncer

Ministerio de Economía y Competitividad

Fundación Eugenio Rodríguez Pascual, Fundació la Marató de TV3

Generalitat de Catalunya

Instituto Carlos III

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ARTICLE ABSTRACT

Snail1 transcriptional factor is essential for triggering epithelial-to-mesenchymal transition (EMT) and inducing tumor cell invasion. We report here an EMT-independent action of Snail1 on tumor invasion, as it is required for the activation of cancer-associated fibroblasts (CAF). Snail1 expression in fibroblasts requires signals derived from tumor cells, such as TGFβ; reciprocally, in fibroblasts, Snail1 organizes a complex program that stimulates invasion of epithelial cells independent of the expression of Snail1 in these cells. Epithelial cell invasion is stimulated by the secretion by fibroblast of diffusible signaling molecules, such as prostaglandin E2. The capability of human or murine CAFs to promote tumor invasion is dependent on Snail1 expression. Inducible Snail1 depletion in mice decreases the invasion of breast tumors; moreover, epithelial tumor cells coxenografted with Snail1-depleted fibroblasts originated tumors with lower invasion than those transplanted with control fibroblasts. Therefore, these results demonstrate that the role of Snail1 in tumor invasion is not limited to EMT, but it is also dependent on its activity in stromal fibroblasts, where it orchestrates the cross-talk with epithelial tumor cells. Cancer Res; 76(21); 6205–17. ©2016 AACR.

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