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Targeting addiction to HMGB2-driven transcriptional programs in pancreatic cancer.

Adi Danieli-Mackay, Ioanna Papadionysiou, Markos Tsitsianopoulos, Fabio Bennet Gätje, Henrik Spahn, Christian Schmidt, Lukas Klein, Shyam Ramasamy, Nadine Übelmesser, Jennifer Appelhans, Olga Dschun, Emre Taylan Duman, Fabian Ludewig, Sebastian Schimkowiak, Matthias Dobbelstein, Gabriela Salinas, Philipp Ströbel, A Marieke Oudelaar, Tiago De Oliveira, Shiv Kishor Singh, Gernot Längst, Lena-Christin Conradi, Argyris Papantonis

Cell reportsSep 22, 2026PMID 42636797doi:10.1016/j.celrep.2026.117649 Journal ArticlepubmedProvenance
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PubMed
Retrieved
Sep 28, 2026
Layer
normalized (units and labels harmonized; values unchanged)
Run
ING-PUBMED-20260928-000001
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Pancreatic cancer remains at a stagnant 5-year survival of <13%, attributed to the high heterogeneity and plasticity of these tumors. To circumvent this, we focus on the abundant nuclear protein high mobility group-box protein 2 (HMGB2). HMGB2 depletion is key for establishing replicative…

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