2018
DOI: 10.1097/dss.0000000000001360
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The Cellular Response of Keloids and Hypertrophic Scars to Botulinum Toxin A: A Comprehensive Literature Review

Abstract: Overall, BoNT-A has the potential to prevent or treat pathologic scars in patients with a known personal or family history of keloids and hypertrophic scars, which may improve patient psychosocial distress and reduce clinic visits and health care costs. Variability in keloid and hypertrophic scar response to BoNT-A may be due to interexperiment differences in dosing, tissue donors, and assay sensitivity.

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Cited by 40 publications
(49 citation statements)
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“…Another theory of mechanism of BoNT‐A on hypertrophic scars and keloids is the effect on cell cycle distribution of fibroblasts. Fibroblasts hyperproliferation is one of the factors that result in hypertrophic scars and keloids . BoNT‐A may directly modulate the activity of fibroblast by altering apoptotic, migratory, and fibrotic pathways on pathological scars and thus improve their appearance .…”
Section: Mechanism Of Action Of Botulinum Toxin Type a On Hypertrophimentioning
confidence: 99%
See 1 more Smart Citation
“…Another theory of mechanism of BoNT‐A on hypertrophic scars and keloids is the effect on cell cycle distribution of fibroblasts. Fibroblasts hyperproliferation is one of the factors that result in hypertrophic scars and keloids . BoNT‐A may directly modulate the activity of fibroblast by altering apoptotic, migratory, and fibrotic pathways on pathological scars and thus improve their appearance .…”
Section: Mechanism Of Action Of Botulinum Toxin Type a On Hypertrophimentioning
confidence: 99%
“…Fibroblasts hyperproliferation is one of the factors that result in hypertrophic scars and keloids. 20 BoNT-A may directly modulate the activity of fibroblast by altering apoptotic, migratory, and fibrotic pathways on pathological scars and thus improve their appearance. 20 Another experiment by Zhibo et al showed BoNT-A does act on fibroblasts directly, but the experiment did not explain how.…”
Section: Bont-a Action On Cell Cycle and Gene Expression Of Fibroblmentioning
confidence: 99%
“…However, the N‐terminal of BTXA light chain has the activity of zinc metalloproteinase, which can cut the synaptosomal‐associated protein of 25 kDa (SNAP‐25) and prevent the release of acetylcholine into the synaptic cleft, thus causing “chemo‐denervation,” reducing the tension on both sides of the wound and affecting the scar morphology . In addition, some evidences suggest that BTXA may affect scar formation by reducing fibroblast proliferation, reducing TGF‐β expression, and altering collagen deposition and remodeling processes . Two experiments by Xiao, Z. et al indicated that BTXA can effectively inhibit the proliferation of fibroblasts derived from hypertrophic scar and further reduce the content of TGF‐β1 and its downstream regulator connective tissue growth factor (CTGF) .…”
Section: Discussionmentioning
confidence: 99%
“…25,26 In addition, some evidences suggest that BTXA may affect scar formation by reducing fibroblast proliferation, reducing TGF-β expression, and altering collagen deposition and remodeling processes. 27 further reduce the content of TGF-β1 28 and its downstream regulator connective tissue growth factor (CTGF). 29 Jeong et al 30 Two meta-analysis results published by Wang 32 and Wang 33 before including 9 studies respectively have showed that BTXA injection is a safe and effective treatment for scar prevention, but some recent studies have reached negative conclusions.…”
Section: Adverse Eventsmentioning
confidence: 99%
“…Keloids mostly affect, but are not limited to, younger patients with higher Fitzpatrick skin phototypes [5]. Keloid scars tend to develop more readily during and after puberty, and disproportionately affect African American, Latin American, and Asian populations with a prevalence ranging from 0.3 to 16% [6].…”
Section: Introductionmentioning
confidence: 99%