2024
DOI: 10.1016/j.gendis.2023.02.027
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Clinical applications of the CRISPR/Cas9 genome-editing system: Delivery options and challenges in precision medicine

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Cited by 20 publications
(12 citation statements)
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References 153 publications
(170 reference statements)
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“…However, this phenomenon can be inhibited by the STING pathway inhibitor amlexanox [ 43 ]. Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated nuclease 9 (Cas9), a simple and easy-to-operate gene editing technology that has a wide range of applications in targeting and preventing severe diseases, including CVDs, has been one of the greatest advances in biomedicine in the last two decades [ 130 ]. Zhao et al [ 131 ] revealed that CRISPR-Cas9 gene editing delivered by an adeno-associated virus ameliorates familial hypercholesterolemia due to low-density lipoprotein receptor (LDLR) mutations, reduces the aortic AS plaque area, and attenuates inflammatory infiltration.…”
Section: Future Expectationsmentioning
confidence: 99%
“…However, this phenomenon can be inhibited by the STING pathway inhibitor amlexanox [ 43 ]. Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated nuclease 9 (Cas9), a simple and easy-to-operate gene editing technology that has a wide range of applications in targeting and preventing severe diseases, including CVDs, has been one of the greatest advances in biomedicine in the last two decades [ 130 ]. Zhao et al [ 131 ] revealed that CRISPR-Cas9 gene editing delivered by an adeno-associated virus ameliorates familial hypercholesterolemia due to low-density lipoprotein receptor (LDLR) mutations, reduces the aortic AS plaque area, and attenuates inflammatory infiltration.…”
Section: Future Expectationsmentioning
confidence: 99%
“…Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 is a promising genetic approach recently emerging as a potentially effective treatment against hyperlipidemia. Compared to the other editing approaches, due to its higher specificity and efficacy, CRISPR/Cas9 has been thoroughly investigated to reduce Lp(a) levels and target the PCSK9 and LPA genes [ 90 ]. A single infusion was found to knock down PCSK9 in almost every hepatocyte of cynomolgus monkeys and lowered LDL-C by up to 60% for a period of 8 months.…”
Section: Future Perspectivesmentioning
confidence: 99%
“… 16 , 44 , 45 , 46 Many of these limitations can be overcome using the CRISPR-Cas9-based gene editing tool as an easy and available method. 47 Accordingly, current research efforts are focused on precise CAR T cell engineering with conventional CRISPR-Cas9 systems or novel editors that can generate the desired mutations with or without inducing a double-stranded DNA break into the genome. 48 These tools and strategies can be directly applied to target negative regulators of T cell function, insert therapeutic genes to specific loci, and generate universal CAR allogeneic T cell products for on-demand immunotherapy ( Fig.…”
Section: Crispr Gene Editing Toolmentioning
confidence: 99%