Extracellular matrix reprogramming by the YAP/TAZ– TGF-ß2 axis drives immune exclusion in cholangiocarcinoma models

YAP and TAZ, key effectors of the Hippo pathway, are often hyperactivated in cancer, promoting tumor progression and therapy resistance. Their oncogenic role depends on interaction with TEAD transcription factors, making the TEAD-YAP/TAZ complex a promising therapeutic target. Using translational mouse models, we showed here that sustained systemic YAP/TAZ depletion caused severe side effects. These could be avoided through pulsed inhibition, which effectively suppressed tumor growth, even at advanced stages. We identified Tgfb2 as a critical YAP/TAZ target gene for tumor formation and demonstrated that YAP/TAZ drove T cell exclusion via activation of tissue remodeling genes. Consequently, YAP/TAZ inhibition enhanced immune cell infiltration. However, infiltrating T cells rapidly underwent exhaustion. Combining YAP/TAZ inhibition with immune checkpoint blockade (ICB) reversed this exhaustion and sensitized resistant tumors to immunotherapy. This combination reshaped the tumor microenvironment to support immune cell infiltration and activation, representing a therapeutic strategy that maximizes anti-tumor immunity while minimizing toxicity.

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Publication Details

Journal
Journal of Clinical Investigation
Published
2026-07-02
DOI
https://doi.org/10.1172/jci201579
Primary Topic
Hippo pathway signaling and YAP/TAZ
Type
article
Field-Weighted Citation Impact
0.00

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article

Extracellular matrix reprogramming by the YAP/TAZ– TGF-ß2 axis drives immune exclusion in cholangiocarcinoma models

Orlando Paciello, Marco Jessen, Sabine Muth, Tina Lehmann et al.
Journal of Clinical Investigation
Hippo pathway signaling and YAP/TAZ
article

Extracellular matrix reprogramming by the YAP/TAZ– TGF-ß2 axis drives immune exclusion in cholangiocarcinoma models

Orlando Paciello, Marco Jessen, Sabine Muth, Tina Lehmann, Tracy T. Tang, Çağla Dönmez, Andreas Rosenwald, Donato Inverso, Shyam Murali, Christin Ritter, Anita Cindric Vranesic, Marie Tollot-Wegner, Evaristo Di Napoli, Celina Junker, Viktoria Haug, Volker Deckert, Yuliya Kurlishchuk, KyungMok Kim, Advitiya Khandelwal, Konrad Bücking, Björn von Eyss, Tanja Deckert-Gaudig, Markus Radsak, Tom Hünniger
article en

Abstract

YAP and TAZ, key effectors of the Hippo pathway, are often hyperactivated in cancer, promoting tumor progression and therapy resistance. Their oncogenic role depends on interaction with TEAD transcription factors, making the TEAD-YAP/TAZ complex a promising therapeutic target. Using translational mouse models, we showed here that sustained systemic YAP/TAZ depletion caused severe side effects. These could be avoided through pulsed inhibition, which effectively suppressed tumor growth, even at advanced stages. We identified Tgfb2 as a critical YAP/TAZ target gene for tumor formation and demonstrated that YAP/TAZ drove T cell exclusion via activation of tissue remodeling genes. Consequently, YAP/TAZ inhibition enhanced immune cell infiltration. However, infiltrating T cells rapidly underwent exhaustion. Combining YAP/TAZ inhibition with immune checkpoint blockade (ICB) reversed this exhaustion and sensitized resistant tumors to immunotherapy. This combination reshaped the tumor microenvironment to support immune cell infiltration and activation, representing a therapeutic strategy that maximizes anti-tumor immunity while minimizing toxicity.

Journal of Clinical Investigation
Vita-Salute San Raffaele University (IT), Johannes Gutenberg University Mainz (DE), University of Würzburg (DE), Leibniz Institute of Photonic Technology (DE), Mateon Therapeutics (United States) (US), University Medical Center of the Johannes Gutenberg University Mainz (DE), Leibniz Institute on Aging - Fritz Lipmann Institute (FLI) (DE), University of Naples Federico II (IT)
Wilhelm Sander-Stiftung, Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Deutsche Krebshilfe
Reduced inequalities
Openalex Percentile: Top 10%
Hippo pathway signaling and YAP/TAZ
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