Esophageal extracellular matrix hydrogel mitigates metaplastic change in a dog model of Barrett’s esophagus
Open accessAbstract
Oral delivery of esophageal extracellular matrix hydrogel mitigates mucosal inflammation and metaplasia in a dog model of reflux.
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Esophageal matrix hydrogel shows a tissue-specific remodeling response in an esophageal cancer dog model, as opposed to a urinary bladder matrix hydrogel.
“while esophageal matrix hydrogel has shown tissue-specific remodeling response in a esophageal cancer dog model, as opposed to an urinary bladder matrix hydrogel [154].”
From Immune Response to Extracellular Matrix Bioscaffolds: A Comprehensive Review (2025) · cites this paper as [154]
The Results section ('eECM hydrogel mitigates metaplastic change in the esophageal mucosa'; page unavailable) reports improvement in dogs with Barrett’s-type metaplasia after esophageal ECM hydrogel treatment. The study did not use an esophageal cancer model or compare the hydrogel with urinary bladder matrix hydrogel: its control dogs received omeprazole only, as stated in the Results section on macroscopic inflammation (page unavailable). Thus it does not establish the claimed tissue-specific response relative to urinary bladder matrix. (LLM, conf=0.90)
Experimental — accuracy not yet measuredECM degradation peptides promote M2-like phenotypes in vitro and in vivo.
“promotion of M2-like phenotypes in vitro [40,44,153] and in vivo [152,154,155].”
From Immune Response to Extracellular Matrix Bioscaffolds: A Comprehensive Review (2025) · cites this paper as [154]
The Discussion (page unavailable) says ECM degradation products promote a shift from proinflammatory macrophages toward a regulatory, anti-inflammatory phenotype in vitro and in vivo. The dog study found fewer TNFα-positive cells after eECM hydrogel treatment, but it did not isolate degradation peptides or establish an M2-like phenotype specifically. (LLM, conf=0.83)
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- Authors
- Naranjo, J. D., Saldin, L. T., Sobieski, E., Quijano, L. M., Hill, R. C., Chan, P. G., Torres, C., Dziki, J. L., Cramer, M. C., Lee, Y. C., Das, R., Bajwa, A. K., Nossair, R., Klimak, M., Marchal, L., Patel, S., Velankar, S. S., Hansen, K. C., McGrath, K., & Badylak, S. F.
- Affiliations
- University of Pittsburgh (US)
- University of Colorado Anschutz (US)
- UPMC Health System (US)
- Corresponding author
- Badylak, Stephen F.
- ORCID
- Venue
- Science Advances
- Published
- 2020-07-03
- Volume
- 6
- Issue
- 27
- Pages
- eaba4526-eaba4526
- ISSN
- 2375-2548 (ISSN-L)
- PMC
- PMC7329334
- OpenAlex
- W3040581353
- Cited by
- 38
- References
- 60
- Citations by year
- 2026: 5 · 2025: 2 · 2024: 6 · 2023: 6 · 2022: 13 · 2021: 4 · 2020: 2
- FWCI
- 5.71
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Science Advances (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Office of Naval Research (N00014-14-1-0723)
- National Cancer Institute (F31CA210694)
- Clinical and Translational Science Institute, University of Pittsburgh (UL1TR001857)
- BARD
- Topics
- Health Sciences › Medicine › Surgery › Esophageal Cancer Research and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
- Health Sciences › Medicine › Gastroenterology › Gastroesophageal reflux and treatments
- Keywords
- Barrett's esophagus, extracellular matrix hydrogel, metaplasia, mucoadhesive hydrogels, inflammation, canine model, tissue engineering
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