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After treatment of hypertrophic scars with different concentrations of paclitaxel, there was a significant decrease in the density of fibroblasts in the scars treated with paclitaxel solution of 96 mg/L or higher comparing with the control group.

After treatment of hypertrophic scars with different concentrations of paclitaxel, there was a significant decrease in the density of fibroblasts in the scars treated with paclitaxel solution of 96 mg/L or higher comparing with the control group.

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Background and objective The onset and progression of pathological scarring involves multiple cytokines and complex mechanisms. However, hyperplasia of fibroblasts and neovascularization plays important roles, which can be inhibited by paclitaxel. The aim of this study was to investigate the efficacy of paclitaxel in the treatment of hypertrophic s...

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... Also, PCT treatment suppresses the production of TNF-α, IL-6 and TGF-β and inhibits the expression of α-SMA and collagen I in human KD fibroblast. PCT-cholesterol-loaded liposome showed a better ability to inhibit cell proliferation, migration and invasion, and effectively promoted apoptosis and arrested cell cycle in G2/M phase compared to PCT alone [133]. In the rabbit's ear model of HTS, PCT reduced the formation of HTS. ...
... Metabolites of mitomycin C also interfere with the synthesis of DNA, RNA and proteins [95][96][97]122]. Liposomal paclitaxel can suppress the production of TNF-α, IL-6 and TGF-β and inhibit the expression of α-SMA and collagen I in human KD fibroblast [133]. Tamoxifen decreases the expression of TGF-β1, with the consequent inhibitions of both fibroblast proliferation and collagen production [135]. ...
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Keloids (KD) and hypertrophic scars (HTS), which are quite raised and pigmented and have increased vascularization and cellularity, are formed due to the impaired healing process of cutaneous injuries in some individuals having family history and genetic factors. These scars decrease the quality of life (QOL) of patients greatly, due to the pain, itching, contracture, cosmetic problems, and so on, depending on the location of the scars. Treatment/prevention that will satisfy patients’ QOL is still under development. In this article, we review pharmacotherapy for treating KD and HTS, including the prevention of postsurgical recurrence (especially KD). Pharmacotherapy involves monotherapy using a single drug and combination pharmacotherapy using multiple drugs, where drugs are administered orally, topically and/or through intralesional injection. In addition, pharmacotherapy for KD/HTS is sometimes combined with surgical excision and/or with physical therapy such as cryotherapy, laser therapy, radiotherapy including brachytherapy, and silicone gel/sheeting. The results regarding the clinical effectiveness of each mono-pharmacotherapy for KD/HTS are not always consistent but rather scattered among researchers. Multimodal combination pharmacotherapy that targets multiple sites simultaneously is more effective than mono-pharmacotherapy. The literature was searched using PubMed, Google Scholar, and Online search engines.
... The dressings were changed once a day after disinfecting with iodophor. Three weeks after wound induction, the scabs fell off naturally and hypertrophic scars were observed [8]. ...
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... This is consistent with the conclusion drawn on a rabbit ear hypertrophic scar model. With paclitaxel treatment, fibroblast proliferation, collagen deposition, and micro-angiogenesis in hypertrophic scars were all downregulated (64). ...
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The underlying mechanisms of wound healing are complex but inflammation is one of the determining factors. Besides its traditional role in combating against infection upon injury, the characteristics and magnitude of inflammation have dramatic impacts on the pathogenesis of scar. Keloids and hypertrophic scars are pathological scars that result from aberrant wound healing. They are characterized by continuous local inflammation and excessive collagen deposition. In this review, we aim at discussing how dysregulated inflammation contributes to the pathogenesis of scar formation. Immune cells, soluble inflammatory mediators, and the related intracellular signal transduction pathways are our three subtopics encompassing the events occurring in inflammation associated with scar formation. In the end, we enumerate the current and potential medicines and therapeutics for suppressing inflammation and limiting progression to scar. Understanding the initiation, progression, and resolution of inflammation will provide insights into the mechanisms of scar formation and is useful for developing effective treatments.
... This exuberant response produces immature leaky blood vessels. The production of new blood vessels provides an environment with easy access to necessary nutrients, signals, and cells essential for coordinating repair (Huang et al. 2015). ...
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... AEîäíèé ç öèõ òåðàïåâòè÷íèõ ï³äõîä³â ñàìî-ñò³éíî àáî â êîìá³íàö³¿ íå çàáåçïå÷óº ñòàá³ëüíó â³äñóòí³ñòü ðåöèäèâó á³ëüøå 70-80 % [10]. Ñïðèéíÿòòÿ êåëî¿äíîãî ðóáöÿ ÿê äîáðîÿê³ñíî¿ ïóõëèíè çóìîâèëî âèêîðèñòàííÿ äëÿ éîãî ë³êóâàííÿ öèòîñòà-òèê³â: 5-ôòîðóðàöèëó [4], áëåîì³öèíó [21] òà ïàêë³òàêñåëó [17]. ...
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Unlabelled: Significance: The aberrant inflammation during wound healing results in pathological scarring, such as hypertrophic scars and keloids. This adversely affects the quality of life of patients due to the disfiguring appearance as well as the symptoms of itch and pain. This review summarizes the up-to-date knowledge of the immunopathogenesis and treatment options for pathological scars. Recent advances: With the advent of new technologies, combined with in vitro and in vivo wound models, several inflammatory cells have been shown to have both direct or indirect effects on both wound healing and pathological scarring. Critical issues: Expansion of pro-fibrotic immune cells such as M2 macrophages, dendritic cells, mast cells, and Th2 cells leads to fibroblast transition to myofibroblasts via TGF-β1 signaling pathway. Appropriate management of such inflammatory responses during wound healing remains a critical issue during clinical practice. Future directions: Regulating inflammation response during wound healing may be a potential therapeutic option for avoiding or reducing pathological scars.
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Hypertrophic scar (HS) is a typical pathological response during skin injury, which can lead to pain, itching, and contracture in patients and even affect their physical and mental health. The complexity of the wound healing process leads to the formation of HS affected by many factors. Several treatments are available for HS, whereas some have more adverse reactions and can even cause new injuries with exacerbated scarring. Traditional Chinese Medicine (TCM) has a rich source, and most botanical drugs have few side effects, providing new ideas and methods for treating HS. This paper reviews the formation process of HS, the therapeutic strategy for HS, the research progress of TCM with its relevant mechanisms in the treatment of HS, and the related new drug delivery system of TCM, aiming to provide ideas for further research of botanical compounds in the treatment of HS, to promote the discovery of more efficient botanical candidates for the clinical treatment of HS, to accelerate the development of the new drug delivery system and the final clinical application, and at the same time, to promote the research on the anti-HS mechanism of multiherbal preparations (Fufang), to continuously improve the quality control and safety and effectiveness of anti-HS botanical drugs in clinical application.