Mesenchymal stem cell therapy for liver fibrosis
Open accessAbstract
Currently, the most effective treatment for end-stage liver fibrosis is liver transplantation; however, transplantation is limited by a shortage of donor organs, surgical complications, immunological rejection, and high medical costs. Recently, mesenchymal stem cell (MSC) therapy has been suggested as an effective alternate approach for the treatment of hepatic diseases. MSCs have the potential to differentiate into hepatocytes, and therapeutic value exists in their immune-modulatory properties and secretion of trophic factors, such as growth factors and cytokines. In addition, MSCs can suppress inflammatory responses, reduce hepatocyte apoptosis, increase hepatocyte regeneration, regress liver fibrosis and enhance liver functionality. Despite these advantages, issues remain; MSCs also have fibrogenic potential and the capacity to promote tumor cell growth and oncogenicity. This paper summarizes the properties of MSCs for regenerative medicine and their therapeutic mechanisms and clinical application in the treatment of liver fibrosis. We also present several outstanding risks, including their fibrogenic potential and their capacity to promote pre-existing tumor cell growth and oncogenicity.
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MSCs can differentiate into hepatocyte-like cells.
“newer research has determined their phenomenal plasticity, including their potency to differentiate into hepatocyte-like cells (HLCs)([39, 40]”
From From signaling pathways to clinical trials: mesenchymal stem cells as multimodal regenerative architects in liver cirrhosis therapy (2025) · cites this paper as [39]
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Cited by
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Suk, K. T., Yoon, J., Kim, M. Y., Kim, C. W., Kim, J. K., Park, H., Hwang, S. G., Kim, D. J., Lee, B. S., Lee, S. H., et al. (2016) · Hepatology · doi:10.1002/hep.28693 · Cited by 303 · see citing works
Self-citationMesenchymal stem cell therapy for liver fibrosis/cirrhosis
Cao, Y., Ji, C., & Lu, L. (2020) · Annals of Translational Medicine · doi:10.21037/atm.2020.02.119 · Cited by 99 · see citing works
Yan, L., Li, D., Li, S., Jiao Li, J., Du, G., Liu, H., Zhang, J., Li, X., Fan, Z., Jiu, J., et al. (2024) · Chemical Engineering Journal · doi:10.1016/j.cej.2024.154432 · Cited by 20 · see citing works
Bozorgi, V., Babaahmadi, M., Salehi, M., Vafaeimanesh, J., & Hajizadeh-Saffar, E. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04535-8 · Cited by 11 · see citing works
“…the ability to generate mesenchymal tissues (bone, cartilage, and fat), newer research has determined their phenomenal plasticity, including their potency to differentiate into hepatocyte-like cells (HLCs)([39, 40] a feature that renders them particularly valuable for liver regeneration therapy.”
Macrophage heterogeneity in liver fibrosis
Wang, W., Li, S., Liu, Y., Ding, X., Yang, Y., Chen, S., Cao, J., Tacke, F., Dong, W., & Lan, T. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1639455 · Cited by 8 · see citing works
- Authors
- Eom, Y. W., Shim, K. Y., & Baik, S. K.
- Affiliations
- Yonsei University (KR)
- Corresponding author
- Baik, Soon Koo
- Venue
- The Korean Journal of Internal Medicine
- Published
- 2015-08-27
- Volume
- 30
- Issue
- 5
- Pages
- 580-589
- ISSN
- 1226-3303 (ISSN-L)
- 2005-6648
- PMC
- PMC4578027
- OpenAlex
- W1794770698
- Cited by
- 226
- References
- 4
- Citations by year
- 2026: 4 · 2025: 13 · 2024: 20 · 2023: 19 · 2022: 19 · 2021: 56 · 2020: 23 · 2019: 21 · 2018: 20 · 2017: 18 · 2016: 12 · 2015: 1
- FWCI
- 2.39
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- The Korean Journal of Internal Medicine (publishedVersion, cc-by-nc)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Funders
- Yonsei University Future-leading Research Initiative
- Topics
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
- Keywords
- mesenchymal stem cells, liver fibrosis, regenerative medicine, hepatocyte differentiation, immunomodulation, hepatocyte regeneration, tumor promotion, oncogenicity, liver transplantation alternatives, clinical application
- MeSH terms
- Animals, Cell Differentiation, Humans, Liver, Liver Cirrhosis, Liver Regeneration, Phenotype, Risk Factors, Signal Transduction, Treatment Outcome, Hepatocytes, Regenerative Medicine, Mesenchymal Stem Cell Transplantation, Cell Proliferation, Mesenchymal Stem Cells
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