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Thrombin contributes to cancer immune evasion via proteolysis of platelet-bound GARP to activate LTGF-β
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Proteolysis of platelet-bound GARP by thrombin liberates active TGF-β and contributes to cancer immune evasion in the tumor microenvironment.
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“Since GARP is also expressed by endothelial cells, fibroblasts, megakaryocytes and platelets73,74”
From TGFβ biology in cancer progression and immunotherapy (2021) · cites this paper as [73]
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Metadata
- Authors
- Metelli, A., Wu, B. X., Riesenberg, B., Guglietta, S., Huck, J. D., Mills, C., Li, A., Rachidi, S., Krieg, C., Rubinstein, M. P., Gewirth, D. T., Sun, S., Lilly, M. B., Wahlquist, A. H., Carbone, D. P., Yang, Y., Liu, B., & Li, Z.
- Affiliations
- Medical University of South Carolina (US)
- Pelotonia (US)
- Hauptman-Woodward Medical Research Institute (US)
- Corresponding author
- Li, Zihai
- ORCID
- Venue
- Science Translational Medicine
- Published
- 2020-01-08
- Volume
- 12
- Issue
- 525
- ISSN
- 1946-6234 (ISSN-L)
- 1946-6242
- PMC
- PMC7814995
- OpenAlex
- W3000560268
- Cited by
- 139
- References
- 68
- Citations by year
- 2026: 21 · 2025: 22 · 2024: 20 · 2023: 26 · 2022: 24 · 2021: 19 · 2020: 7
- FWCI
- 6.16
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science Translational Medicine (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (P01CA186866)
- National Institute of Allergy and Infectious Diseases (R01AI077283)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
- Health Sciences › Medicine › Hematology › Blood Coagulation and Thrombosis Mechanisms
- Health Sciences › Medicine › Hematology › Platelet Disorders and Treatments
- Keywords
- thrombin, tumor immune evasion, GARP, latent TGF-beta1, platelets, proteolysis, tumor microenvironment, antitumor immunity, PD-1 immune checkpoint blockade, circulating biomarkers, thrombin inhibition
- MeSH terms
- Immune Checkpoint Inhibitors, Animals, Blood Platelets, Cell Membrane, Humans, Membrane Proteins, Mice, Inbred BALB C, Mice, Inbred C57BL, Neoplasms, Protein Binding, Thrombin, Disease Progression, Latent TGF-beta Binding Proteins, Immune Evasion, Tumor Microenvironment, Proteolysis, Carcinogenesis
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