Abstract
Purpose of review: This review aims to evaluate the potential of CRISPR-based gene editing tools, particularly prime editors (PE), in treating genetic cardiac diseases. It seeks to answer how these tools can overcome current therapeutic limitations and explore the synergy between PE and induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) for personalized medicine. Recent findings: Recent advancements in CRISPR technology, including CRISPR-Cas9, base editors, and PE, have demonstrated precise genome correction capabilities. Notably, PE has shown exceptional precision in correcting genetic mutations. Combining PE with iPSC-CMs has emerged as a robust platform for disease modeling and developing innovative treatments for genetic cardiac diseases. Summary: The review finds that PE, when combined with iPSC-CMs, holds significant promise for treating genetic cardiac diseases by addressing their root causes. This approach could revolutionize personalized medicine, offering more effective and precise treatments. Future research should focus on refining these technologies and their clinical applications.
Original language | English |
---|---|
Pages (from-to) | 1197-1208 |
Number of pages | 12 |
Journal | Current cardiology reports |
Volume | 26 |
Issue number | 11 |
Early online date | 11 Sept 2024 |
DOIs | |
Publication status | Published - Nov 2024 |
Keywords
- Cellular reprogramming
- CRISPR-based gene editing
- Gene therapy
- Genetic cardiac diseases
- Prime editing
Access to Document
10.1007/s11886-024-02118-2Licence: CC BY
s11886-024-02118-2Final published version, 1.17 MBLicence: CC BY
Other files and links
Fingerprint
Dive into the research topics of 'Integrating Prime Editing and Cellular Reprogramming as Novel Strategies for Genetic Cardiac Disease Modeling and Treatment'. Together they form a unique fingerprint.
View full fingerprint
Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver
Yao, B., Lei, Z., Gonçalves, M. A. F. V. (2024). Integrating Prime Editing and Cellular Reprogramming as Novel Strategies for Genetic Cardiac Disease Modeling and Treatment. Current cardiology reports, 26(11), 1197-1208. https://doi.org/10.1007/s11886-024-02118-2
Yao, Bing ; Lei, Zhiyong ; Gonçalves, Manuel A.F.V. et al. / Integrating Prime Editing and Cellular Reprogramming as Novel Strategies for Genetic Cardiac Disease Modeling and Treatment. In: Current cardiology reports. 2024 ; Vol. 26, No. 11. pp. 1197-1208.
@article{d865b3f41ae540d7af93902bfca78867,
title = "Integrating Prime Editing and Cellular Reprogramming as Novel Strategies for Genetic Cardiac Disease Modeling and Treatment",
abstract = "Purpose of review: This review aims to evaluate the potential of CRISPR-based gene editing tools, particularly prime editors (PE), in treating genetic cardiac diseases. It seeks to answer how these tools can overcome current therapeutic limitations and explore the synergy between PE and induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) for personalized medicine. Recent findings: Recent advancements in CRISPR technology, including CRISPR-Cas9, base editors, and PE, have demonstrated precise genome correction capabilities. Notably, PE has shown exceptional precision in correcting genetic mutations. Combining PE with iPSC-CMs has emerged as a robust platform for disease modeling and developing innovative treatments for genetic cardiac diseases. Summary: The review finds that PE, when combined with iPSC-CMs, holds significant promise for treating genetic cardiac diseases by addressing their root causes. This approach could revolutionize personalized medicine, offering more effective and precise treatments. Future research should focus on refining these technologies and their clinical applications.",
keywords = "Cellular reprogramming, CRISPR-based gene editing, Gene therapy, Genetic cardiac diseases, Prime editing",
author = "Bing Yao and Zhiyong Lei and Gon{\c c}alves, {Manuel A.F.V.} and Sluijter, {Joost P.G.}",
note = "Publisher Copyright: {\textcopyright} The Author(s) 2024.",
year = "2024",
month = nov,
doi = "10.1007/s11886-024-02118-2",
language = "English",
volume = "26",
pages = "1197--1208",
journal = "Current cardiology reports",
issn = "1523-3782",
publisher = "Current Medicine Group",
number = "11",
}
Yao, B, Lei, Z, Gonçalves, MAFV 2024, 'Integrating Prime Editing and Cellular Reprogramming as Novel Strategies for Genetic Cardiac Disease Modeling and Treatment', Current cardiology reports, vol. 26, no. 11, pp. 1197-1208. https://doi.org/10.1007/s11886-024-02118-2
Integrating Prime Editing and Cellular Reprogramming as Novel Strategies for Genetic Cardiac Disease Modeling and Treatment. / Yao, Bing; Lei, Zhiyong; Gonçalves, Manuel A.F.V. et al.
In: Current cardiology reports, Vol. 26, No. 11, 11.2024, p. 1197-1208.
Research output: Contribution to journal › Article › Academic › peer-review
TY - JOUR
T1 - Integrating Prime Editing and Cellular Reprogramming as Novel Strategies for Genetic Cardiac Disease Modeling and Treatment
AU - Yao, Bing
AU - Lei, Zhiyong
AU - Gonçalves, Manuel A.F.V.
AU - Sluijter, Joost P.G.
N1 - Publisher Copyright:© The Author(s) 2024.
PY - 2024/11
Y1 - 2024/11
N2 - Purpose of review: This review aims to evaluate the potential of CRISPR-based gene editing tools, particularly prime editors (PE), in treating genetic cardiac diseases. It seeks to answer how these tools can overcome current therapeutic limitations and explore the synergy between PE and induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) for personalized medicine. Recent findings: Recent advancements in CRISPR technology, including CRISPR-Cas9, base editors, and PE, have demonstrated precise genome correction capabilities. Notably, PE has shown exceptional precision in correcting genetic mutations. Combining PE with iPSC-CMs has emerged as a robust platform for disease modeling and developing innovative treatments for genetic cardiac diseases. Summary: The review finds that PE, when combined with iPSC-CMs, holds significant promise for treating genetic cardiac diseases by addressing their root causes. This approach could revolutionize personalized medicine, offering more effective and precise treatments. Future research should focus on refining these technologies and their clinical applications.
AB - Purpose of review: This review aims to evaluate the potential of CRISPR-based gene editing tools, particularly prime editors (PE), in treating genetic cardiac diseases. It seeks to answer how these tools can overcome current therapeutic limitations and explore the synergy between PE and induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) for personalized medicine. Recent findings: Recent advancements in CRISPR technology, including CRISPR-Cas9, base editors, and PE, have demonstrated precise genome correction capabilities. Notably, PE has shown exceptional precision in correcting genetic mutations. Combining PE with iPSC-CMs has emerged as a robust platform for disease modeling and developing innovative treatments for genetic cardiac diseases. Summary: The review finds that PE, when combined with iPSC-CMs, holds significant promise for treating genetic cardiac diseases by addressing their root causes. This approach could revolutionize personalized medicine, offering more effective and precise treatments. Future research should focus on refining these technologies and their clinical applications.
KW - Cellular reprogramming
KW - CRISPR-based gene editing
KW - Gene therapy
KW - Genetic cardiac diseases
KW - Prime editing
UR - http://www.scopus.com/inward/record.url?scp=85203553348&partnerID=8YFLogxK
U2 - 10.1007/s11886-024-02118-2
DO - 10.1007/s11886-024-02118-2
M3 - Article
C2 - 39259489
AN - SCOPUS:85203553348
SN - 1523-3782
VL - 26
SP - 1197
EP - 1208
JO - Current cardiology reports
JF - Current cardiology reports
IS - 11
ER -
Yao B, Lei Z, Gonçalves MAFV, Sluijter JPG. Integrating Prime Editing and Cellular Reprogramming as Novel Strategies for Genetic Cardiac Disease Modeling and Treatment. Current cardiology reports. 2024 Nov;26(11):1197-1208. Epub 2024 Sept 11. doi: 10.1007/s11886-024-02118-2