Genetic Engineering of Mesenchymal Stem Cells and Its Application in Human Disease Therapy
Open accessAbstract
The use of stem cells for tissue regeneration and repair is advancing both at the bench and bedside. Stem cells isolated from bone marrow are currently being tested for their therapeutic potential in a variety of clinical conditions including cardiovascular injury, kidney failure, cancer, and neurological and bone disorders. Despite the advantages, stem cell therapy is still limited by low survival, engraftment, and homing to damage area as well as inefficiencies in differentiating into fully functional tissues. Genetic engineering of mesenchymal stem cells is being explored as a means to circumvent some of these problems. This review presents the current understanding of the use of genetically engineered mesenchymal stem cells in human disease therapy with emphasis on genetic modifications aimed to improve survival, homing, angiogenesis, and heart function after myocardial infarction. Advancements in other disease areas are also discussed.
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MSCs overexpressing the survival protein AKT release higher levels of the paracrine factors FGF-2, HGF, IGF-1 and VEGF.
“As an example, MSCs overexpressing the survival protein AKT release higher levels of the paracrine factors FGF-2, HGF, IGF-1 and VEGF [151].”
From Mesenchymal stem cell secretome for regenerative medicine: Where do we stand? (2025) · cites this paper as [151]
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Mesenchymal stem cell secretome for regenerative medicine: Where do we stand?
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“Indeed, VEGF promotes angiogenesis and restoring tissues, further highlighting its pivotal role in several tissue injuries, namely in myocardial infarction, wound healing, ischemic stroke, among others [151].”
- Authors
- Hodgkinson, C. P., Gomez, J. A., Mirotsou, M., & Dzau, V. J.
- Affiliations
- Duke Medical Center (US)
- Duke University Medical Center and Mandel Center for Hypertension and Atherosclerosis Research
- Corresponding author
- Dzau, Victor J.
- Venue
- Human Gene Therapy
- Publisher
- SAGE Publications
- Published
- 2010-10-22
- Volume
- 21
- Issue
- 11
- Pages
- 1513-1526
- ISSN
- 1043-0342 (ISSN-L)
- 1557-7422
- PMC
- PMC2978545
- OpenAlex
- W2163899718
- Cited by
- 150
- References
- 6
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 7 · 2023: 5 · 2022: 6 · 2021: 10 · 2020: 8 · 2019: 11 · 2018: 13 · 2017: 8 · 2016: 14 · 2015: 7 · 2014: 11 · 2013: 18 · 2012: 14
- FWCI
- 1.63
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Human Gene Therapy (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DukeSpace (Duke University) (submittedVersion, cc-by-nc-nd)
- Funders
- National Heart, Lung, and Blood Institute (HL 73219, HL 72010, HL81744, R01HL072010, R01-HL35610, R01HL035610, R01HL073219, R01HL081744)
- Topics
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Keywords
- mesenchymal stem cells, genetic engineering, stem cell therapy, bone marrow-derived stem cells, stem cell homing, engraftment, angiogenesis, myocardial infarction, tissue regeneration, cardiovascular damage, renal failure, cancer, neurological disorders, bone disease
- MeSH terms
- Cardiovascular Diseases, Cell Differentiation, Clinical Trials as Topic, Genetic Engineering, Humans, Neoplasms, Nervous System Diseases, Osteogenesis, Bone Marrow Transplantation, Mesenchymal Stem Cell Transplantation, Renal Insufficiency, Mesenchymal Stem Cells
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