Abstract 3363: Fibroblast exosomes induce stromal matrix assembly and breast tumor growth and metastasis
Abstract Stromal matrix assembly is a key feature of aggressive tumors and is associated with poor prognosis of breast cancer patients. Fibronectin is a key stromal matrix molecule whose assembly into fibrils is thought to require cells and which serves as a template for stromal matrix assembly. Fibroblasts are the major cell type that secretes and assembles fibronectin and stromal matrix. Here, we identify that small exosome-type small EVs secreted by fibroblasts are critical initiators of fibronectin assembly, revealing a previously unrecognized mechanism of stromal matrix formation. Fibroblasts engineered to be deficient in exosome secretion showed greatly reduced assembly of fibronectin and other stromal matrix molecules in 2D, 3D, and in vivo environments, and led to reduced tumor growth and lung metastasis by triple-negative breast cancer cells. Furthermore, transgenic mice with defects in exosome secretion had greatly reduced lung fibrosis after treatment with bleomycin. In a direct test of exosome function on fibronectin assembly, we find that the addition of purified small EVs to purified soluble fibronectin in a cell-free system is sufficient to induce fibronectin assembly. The EV-induced fibronectin assembly requires the presence of fibronectin-binding integrins and syndecan-1 in the EVs. We propose a new model in which secreted exosomes directly drive stromal matrix assembly and tissue fibrosis. Citation Format: Bong Hwan Sung, Merlyn Emmanuel, Metti Gari, Jorge Guerrero, Maria Virumbrales-Muñoz, David Inman, Evan Krystofiak, Alan Rapraeger, Suzanne M. Ponik, Alissa M. Weaver. Fibroblast exosomes induce stromal matrix assembly and breast tumor growth and metastasis [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 3363.
Authors
- Metti K. Gari (ORCID: https://orcid.org/0000-0002-6381-3696)
- Evan Krystofiak (ORCID: https://orcid.org/0000-0002-0043-6977)
- Alissa M. Weaver (ORCID: https://orcid.org/0000-0002-4096-8636)
- Bong Hwan Sung (ORCID: https://orcid.org/0000-0002-8140-4685)
- Merlyn Emmanuel
- Alan C. Rapraeger (ORCID: https://orcid.org/0000-0003-1719-3286)
- Suzanne M. Ponik (ORCID: https://orcid.org/0000-0003-1367-4349)
- Marı́a Virumbrales-Muñoz (ORCID: https://orcid.org/0000-0003-3660-8651)
- Jorge F. Guerrero (ORCID: https://orcid.org/0000-0002-4510-5151)
- David Inman
Institutions
- University of Wisconsin–Madison (US)
- University of British Columbia (CA)
- Vanderbilt University (US)
- Wisconsin Division of Public Health (US)
Publication Details
- Journal
- Cancer Research
- Published
- 2026-04-03
- DOI
- https://doi.org/10.1158/1538-7445.am2026-3363
- Primary Topic
- Extracellular vesicles in disease
- Type
- article
- Field-Weighted Citation Impact
- 0.00