c-Rel drives pancreatic cancer metastasis through Fibronectin-Integrin signaling-induced isolation stress resistance and EMT activation.

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Tác giả: M Adli, J Ai, S Alcalá, H Algül, D Bakırdöğen, A Berninger, N F Chhabra, C Dai, D Demircioğlu, K N Diakopoulos, M J Fernandez-Aceñero, K Frank, F Fusco, K Görgülü, E Kaya-Aksoy, L Kohlmann, M Lesina, J C López-Gil, J Martinez-Useros, H Öztürk, K Peschke, R Ranjan, M Reichert, D A Ruess, L Ruiz-Cañas, B Sainz, R M Schmid, F Schmidt, K Steiger, N Wu, J Xin

Ngôn ngữ: eng

Ký hiệu phân loại: 181.4 *India

Thông tin xuất bản: United States : bioRxiv : the preprint server for biology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 643079

Pancreatic ductal adenocarcinoma remains one of the deadliest malignancies, with limited treatment options and a high recurrence rate. Recurrence happens often with metastasis, for which cancer cells must adapt to isolation stress to successfully colonize distant organs. While the fibronectin-integrin axis has been implicated in this adaptation, its regulatory mechanisms require further elaboration. Here, we identify c-Rel as an oncogenic driver in PDAC, promoting epithelial-to-mesenchymal transition (EMT) plasticity, extracellular matrix (ECM) remodeling, and resistance to isolation stress. Mechanistically, c-Rel directly regulates fibronectin (
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