Tumor-derived fibulin-3 activates pro-invasive NF-κB signaling in glioblastoma cells and their microenvironment
Autor: | Vivek Bhaskaran, Bin Hu, Aneta Kwiatkowska, Mohan Sobhana Nandhu, Mariano S. Viapiano, Josie Hayes |
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Rok vydání: | 2017 |
Předmět: |
Male
0301 basic medicine Cancer Research TIMP3 CYLD Mice Nude ADAM17 Protein Biology Receptors Tumor Necrosis Factor Article 03 medical and health sciences Growth factor receptor Cell Line Tumor Glioma Tumor Virus Biomarkers Tumor Tumor Microenvironment Genetics medicine Animals Humans Neoplasm Invasiveness Molecular Biology Cell Proliferation TACE ADAM17 Tumor microenvironment Brain Neoplasms Tumor Necrosis Factor-alpha Calcium-Binding Proteins NF-kappa B Extracellular matrix Tumor-Derived medicine.disease Cell biology Fibulin 030104 developmental biology Tumor progression Disease Progression Tumor Necrosis Factor alpha Signal transduction Glioblastoma glioma invasion Signal Transduction |
Zdroj: | Oncogene |
ISSN: | 1476-5594 0950-9232 |
DOI: | 10.1038/onc.2017.109 |
Popis: | Molecular profiling of glioblastomas has revealed the presence of key signaling hubs that contribute to tumor progression and acquisition of resistance. One of these main signaling mechanisms is the nuclear factor-kappa B (NF-κB) pathway, which integrates multiple extracellular signals into transcriptional programs for tumor growth, invasion and maintenance of the tumor-initiating population. We show here that an extracellular protein released by glioblastoma cells, fibulin-3, drives oncogenic NF-κB in the tumor and increases NF-κB activation in peritumoral astrocytes. Fibulin-3 expression correlates with a NF-κB-regulated 'invasive signature' linked to poorer survival, being a possible tissue marker for regions of active tumor progression. Accordingly, fibulin-3 promotes glioblastoma invasion in a manner that requires NF-κB activation both in the tumor cells and their microenvironment. Mechanistically, we found that fibulin-3 activates the metalloprotease ADAM17 by competing with its endogenous inhibitor, TIMP3. This results in sustained release of soluble tumor necrosis factor alpha (TNFα) by ADAM17, which in turn activates TNF receptors and canonical NF-κB signaling. Taken together, our results underscore fibulin-3 as a novel extracellular signal with strong activating effect on NF-κB in malignant gliomas. Because fibulin-3 is produced de novo in these tumors and is absent from the normal brain, we propose that targeting the fibulin-3/NF-κB axis may provide a novel avenue to disrupt oncogenic NF-κB signaling in combination therapies for malignant brain tumors. |
Databáze: | OpenAIRE |
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