Therapeutic Dressings and Wound Healing Applications 2020
DOI: 10.1002/9781119433316.ch10
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Gene Therapy for the Treatment of Chronic Wounds

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Cited by 4 publications
(3 citation statements)
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“…Gene augmentation, as a prominent strategy, addresses deficiencies resulting from impaired genes in wounds and facilitates the expression of specific proteins crucial for wound healing 88 . Gene augmentation regulates angiogenesis in wound healing and can be achieved by inserting DNA or mRNA into the target cells.…”
Section: Gene Therapy‐based Skin Substitutesmentioning
confidence: 99%
See 1 more Smart Citation
“…Gene augmentation, as a prominent strategy, addresses deficiencies resulting from impaired genes in wounds and facilitates the expression of specific proteins crucial for wound healing 88 . Gene augmentation regulates angiogenesis in wound healing and can be achieved by inserting DNA or mRNA into the target cells.…”
Section: Gene Therapy‐based Skin Substitutesmentioning
confidence: 99%
“…86 We designed and synthesised a multi-functional pro-angiogenic molecule by grafting LXW7 and collagen-binding peptides (SILY) to a dermatan sulfate Gene augmentation, as a prominent strategy, addresses deficiencies resulting from impaired genes in wounds and facilitates the expression of specific proteins crucial for wound healing. 88 Gene augmentation regulates angiogenesis in wound healing and can be achieved by inserting DNA or mRNA into the target cells. Key signalling pathways crucial for wound healing encompass those triggered by FGF, VEGF, transforming growth factor β1 (TGF-β1), hypoxiainducible factor-1α (HIF-1α) and platelet-derived growth factor (PDGF).…”
Section: Peptidesmentioning
confidence: 99%
“…23 , 24 It can offer selective correction of critical angiogenesis pathways that are dysregulated or defective at their genetic roots. 25 The most commonly explored therapeutic molecules for the modulation of gene expression include plasmid DNA (pDNA) and messenger RNA (mRNA) for overexpression of genes, and smaller short interfering RNA (siRNA), microRNA (miRNA), oligonucleotides, and aptamers for post-translational gene silencing. 26 In addition, the gene-editing tool clustered regularly interspaced short palindromic repeats (CRISPR) is boosting the development of new gene-therapy-based medicines.…”
Section: Introductionmentioning
confidence: 99%