脂肪细胞来源干细胞治疗中度放射性皮炎的作用:动物模型。

Cristina Pires Camargo, Juan Pablo Menendez Zavala, Gabriela Park Serafim, Heloisa Andrade Carvalho, Bianca Loula Santos, Viviane Abreu Nunes, Miyuki Uno, Maria José Ferreira Alves, Tatiane Katsue Furuya, Rolf Gemperli
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引用次数: 0

摘要

目的:癌症治疗经常涉及使用放射治疗,这与几种不良反应有关,包括疲劳、免疫抑制和放射性皮炎。放射性皮炎影响全世界高达95%的患者。本研究旨在评估脂肪来源干细胞(ASCs)在大鼠模型中治疗放射性皮炎的治疗潜力。材料与方法:取3只大鼠腹股沟脂肪,分离ASC。然后,20只雄性Wistar大鼠使用两个锶-90斑块进行放射性皮炎诱导,每个斑块向背部区域提供单剂量的18 Gy。15天后,将动物分为两组。(1)对照组(n = 10):未经治疗;(2) ASC组(n = 10):放射性皮炎部位皮下注射1 × 106个ASC。再过15天,用RTOG量表评估皮肤,并收集组织样本进行组织学和炎症标志物的基因表达。结果:根据RTOG评分,ASC组放射性皮炎程度较低。与对照组相比,ASC组小动脉数量增加(p = .007),炎症细胞数量减少(p = .02)。此外,与对照组相比,治疗导致ASC中炎症标志物Il1rap (p Mmp3 (p = 0.001)和Tnf (p = 0.004)的基因表达水平降低约50%,Cd68表达降低30% (p = 0.026)。结论:本研究提示ASC的应用可通过减轻炎症来促进放射性皮炎创面愈合过程。这种方法显示出改善放疗患者预后和生活质量的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of adipocyte-derived stem cells treatment for moderate radiodermatitis: animal model.

Purpose: Cancer treatment frequently involves the use of radiotherapy, which is associated with several adverse effects, including fatigue, immunosuppression, and radiodermatitis. Radiodermatitis affects up to 95% of patients worldwide. This study aimed to evaluate the therapeutic potential of adipose-derived stem cells (ASCs) in treating radiodermatitis in a rat model.

Materials and methods: Inguinal fat of three rats was removed, and ASC isolated. Then, 20 male Wistar rats underwent radiodermatitis induction using two Strontium-90 plaques, each delivering a single dose of 18 Gy to dorsal areas. After 15 days, animals were divided into two groups. (1) Control group (n = 10): without treatment; (2) ASC group (n = 10): treated with subcutaneous 1 × 106 ASC injections into radiodermatitis sites. After 15 more days, skin was evaluated with RTOG scale, and tissue samples were collected to perform histology and gene expression of inflammatory markers.

Results: ASC group showed a lower degree of radiodermatitis according to the RTOG scale. ASC showed an increased number of arterioles (p = .007) and a reduction in number of inflammatory cells (p = .02) compared to control. Furthermore, the treatment led to approximately a 50% reduction in the gene expression levels of the inflammation markers Il1rap (p < .001), Mmp3 (p = .001), and Tnf (p = .004) as well as a 30% reduction in Cd68 (p = .026) expression in ASC when compared to control.

Conclusions: This study suggests that the application of ASC enhances wound healing process in radiodermatitis by mitigating inflammation. This approach shows potential to improve outcomes and quality of life for patients undergoing radiotherapy.

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