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ResearchIn-Press PreviewCell biologyMetabolismOncology Open Access | 10.1172/jci.insight.204554

Tumor stiffness creates a ferroptotic Achilles’ heel through YAP–SKP2 signaling

Emma Villares,1 Nico Taber,1 Shao-Chin Wu,2 Connor Amelung,1 Jianli Wu,2 Chao-Chieh Lin,2 Jen-Tsan Chi,2 and Sharon Gerecht1

1Department of Biomedical Engineering, Duke University, Durham, United States of America

2Department of Molecular Genetics & Microbiology, Duke University, Durham, United States of America

Find articles by Villares, E. in: PubMed | Google Scholar

1Department of Biomedical Engineering, Duke University, Durham, United States of America

2Department of Molecular Genetics & Microbiology, Duke University, Durham, United States of America

Find articles by Taber, N. in: PubMed | Google Scholar

1Department of Biomedical Engineering, Duke University, Durham, United States of America

2Department of Molecular Genetics & Microbiology, Duke University, Durham, United States of America

Find articles by Wu, S. in: PubMed | Google Scholar

1Department of Biomedical Engineering, Duke University, Durham, United States of America

2Department of Molecular Genetics & Microbiology, Duke University, Durham, United States of America

Find articles by Amelung, C. in: PubMed | Google Scholar

1Department of Biomedical Engineering, Duke University, Durham, United States of America

2Department of Molecular Genetics & Microbiology, Duke University, Durham, United States of America

Find articles by Wu, J. in: PubMed | Google Scholar

1Department of Biomedical Engineering, Duke University, Durham, United States of America

2Department of Molecular Genetics & Microbiology, Duke University, Durham, United States of America

Find articles by Lin, C. in: PubMed | Google Scholar |

1Department of Biomedical Engineering, Duke University, Durham, United States of America

2Department of Molecular Genetics & Microbiology, Duke University, Durham, United States of America

Find articles by Chi, J. in: PubMed | Google Scholar |

1Department of Biomedical Engineering, Duke University, Durham, United States of America

2Department of Molecular Genetics & Microbiology, Duke University, Durham, United States of America

Find articles by Gerecht, S. in: PubMed | Google Scholar

Published October 22, 2026 - More info

JCI Insight. https://doi.org/10.1172/jci.insight.204554.
Copyright © 2026, Villares et al. This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Published October 22, 2026 - Version history
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Abstract

Matrix stiffness is a hallmark of aggressive solid tumors and strongly associated with therapeutic resistance and poor prognosis. This mechanical barrier represents a major unmet challenge in oncology, as current strategies rarely address how matrix mechanics themselves drive treatment resistance. Here, we identified ferroptosis, an iron-dependent form of cell death, as a potential long-sought vulnerability that can be exploited to eliminate mechanically resistant tumors. Using genetic and chemical approaches, we investigated how matrix stiffness sensitizes cancer cells to ferroptosis and whether this vulnerability can be therapeutically targeted. We found that cancer cells cultured on stiff matrices were more sensitive to ferroptosis than those on soft matrices, as evidenced by reduced cell viability and elevated lipid peroxidation. Furthermore, we found that matrix stiffness induced YAP activation, which upregulated its target gene SKP2, a key mediator required for the heightened ferroptosis sensitivity observed under stiff conditions. Finally, using an injectable hydrogel system, we demonstrated that stiffened tumors were resistant to chemotherapy but remained highly susceptible to ferroptosis induction, resulting in markedly reduced tumor volume and weight. Our findings established ferroptosis as a stiffness-dependent vulnerability mediated by a YAP-SKP2 signaling axis, revealing a mechanotransductive pathway that may be leveraged to target treatment-refractory tumors.

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