The DOI matches its Crossref record; 221 of the 221 references it cites were found in a registry or an index.
TGF‐β as a driver of fibrosis: physiological roles and therapeutic opportunities
Abstract
Many chronic diseases are marked by fibrosis, which is defined by an abundance of activated fibroblasts and excessive deposition of extracellular matrix, resulting in loss of normal function of the affected organs. The initiation and progression of fibrosis are elaborated by pro‐fibrotic cytokines, the most critical of which is transforming growth factor‐β1 (TGF‐β1). This review focuses on the fibrogenic roles of increased TGF‐β activities and underlying signaling mechanisms in the activated fibroblast population and other cell types that contribute to progression of fibrosis. Insight into these roles and mechanisms of TGF‐β as a universal driver of fibrosis has stimulated the development of therapeutic interventions to attenuate fibrosis progression, based on interference with TGF‐β signaling. Their promise in preclinical and clinical settings will be discussed. © 2021 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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Cited by
Immune cell dysregulation as a mediator of fibrosis in systemic sclerosis
Fang, D., Chen, B., Lescoat, A., Khanna, D., & Mu, R. (2022) · Nature Reviews Rheumatology · doi:10.1038/s41584-022-00864-7 · Cited by 84
Reininger, D., Fundel‐Clemens, K., Mayr, C. H., Wollin, L., Laemmle, B., Quast, K., Nickolaus, P., & Herrmann, F. E. (2024) · British Journal of Pharmacology · doi:10.1111/bph.17303 · Cited by 48
“Its increased signalling not only affects the activated fibroblast population but also influences other cell types that actively contribute to the progression of IPF (Budi et al., 2021).”
Inhibition of TGFβ1 activation prevents radiation-induced lung fibrosis
Yi, M., Yuan, Y., Ma, L., Li, L., Qin, W., Wu, B., Zheng, B., Liao, X., Hu, G., & Liu, B. (2024) · Clinical and Translational Medicine · doi:10.1002/ctm2.1546 · Cited by 33
Control of fibrosis with enhanced safety via asymmetric inhibition of prolyl‐tRNA synthetase 1
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Haga, M., Iida, K., & Okada, M. (2024) · iScience · doi:10.1016/j.isci.2024.109708 · Cited by 19
Metadata
- Authors
- Budi, E. H., Schaub, J. R., Decaris, M., Turner, S., & Derynck, R.
- Venue
- The Journal of Pathology
- Publisher
- Wiley
- Published
- 2021-05-19
- Volume
- 254
- Issue
- 4
- Pages
- 358-373
- ISSN
- 0022-3417 (ISSN-L)
- 1096-9896
- OpenAlex
- W3149662796
- Cited by
- 292
- References
- 221
- FWCI
- 10.87
- Type
- journal article
- Language
- en
- Open access
- closed
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- Budi, E. H., Schaub, J. R., Decaris, M., Turner, S., & Derynck, R. (2021). TGF‐β as a driver of fibrosis: physiological roles and therapeutic opportunities. The Journal of Pathology. https://doi.org/10.1002/path.5680
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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