Nature communications · 2026
Uncovering the signaling networks of disseminated glioblastoma cells in vivo with INSIGHT.
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Ahn Ryuhjin, D'Souza Alicia D, Long Lawrence, Cui Yufei, Gantchev Jennifer, Baquer Gerard, Burgenske Danielle, Bakken Katrina K, Ott Lauren L, Carlson Brett L, Zhou Grace, Kohale Ishwar N, Whittaker Charles A, Temple Heidi, Yaron-Barir Tomer M, Wyckoff Jeffrey, Burns Terry C, Vaubel Rachael A, Flower Cameron T, Huang Wei, Tuma Ann, Johnson Jared L, Agar Nathalie Y R, Ursini-Siegel Josie, Jann Sarkaria, White Forest M
Аннотация
Dysregulation of intracellular signaling networks underpins cancer. Yet, resolving signaling networks within distinct or rare cell types in cancer in vivo has been unattainable. Here we develop INSIGHT by integrating cell sorting with mass spectrometry to enable quantitative phosphoproteomics and proteomics of discrete cell types from fixed tissues. Using INSIGHT, we map the signaling network within disseminating glioblastoma cells from patient-derived xenografts implanted in mice. Disseminating tumor cells undergo a proteome-wide shift from proliferative to mesenchymal, neural progenitor-like cell states. In parallel, signaling network and global kinase activity are rewired, transitioning from cell cycle-associated circuitries to those governing synaptic function, neuronal migration, and ion channel activity. Changes begin at the tumor margin and persist in distant brain parenchyma. Hornerin and phosphorylation of Ca²⁺-permeable GluA2 at Y876 were identified as mediators of glioblastoma progression. INSIGHT enables systems-level dissection of cell-type-specific signaling circuitries in vivo across wide range of biological systems.