Stephanie Arndt, Petra Unger, Irina Ivanova, Wolfgang Bäumler, Konstantin Drexler, Mark Berneburg, Sigrid Karrer
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The present study investigated the effects of combining CAP with ALA-PDT on cutaneous AK and SCC induced by ultraviolet B (UV-B) irradiation in SKH1 hairless mice. <b>Methods:</b> We compared various application sequences (CAP-ALA-red light, ALA-red light-CAP, and ALA-CAP-red light) against conventional ALA-PDT using visual, histological, and molecular assessments of the affected skin. <b>Results:</b> The results demonstrated that combined treatments strongly inhibited the growth of UV-B-induced skin lesions. TUNEL staining revealed increased apoptosis following both single and combined therapies, while Ki-67 staining indicated reduced keratinocyte proliferation and diminished DNA damage in treated areas. mRNA expression analysis showed the upregulation of apoptosis-related genes (<i>p16<sup>INK4a</sup></i>, <i>p21<sup>CIP1</sup></i>) alongside enhanced anti-tumor immune responses (<i>IL-6</i>, <i>IL-8</i>) in the affected tissue samples. 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引用次数: 0
摘要
背景/目的:光化性角化病(AK)发生在阳光损伤的皮肤上,被认为是鳞状细胞癌(SCC)的前兆。光动力疗法(PDT),使用5-氨基乙酰丙酸(ALA)和红光,是AK的常用治疗方法。然而,由于光敏剂的渗透和分布不佳,其对侵袭性肿瘤如SCC的临床疗效受到限制。冷大气等离子体(CAP)是一种部分电离的气体,通过产生活性氧(ROS)来增加皮肤的渗透性并表现出抗癌特性。在先前的一项研究中,CAP与ALA-PDT联合体外治疗SCC细胞显示出良好的协同效应。本研究探讨了CAP联合ALA-PDT对紫外线B (UV-B)照射下SKH1无毛小鼠皮肤AK和SCC的影响。方法:我们对不同的应用序列(cap - ala -红光、ala -红光- cap和ala - cap -红光)与传统的ALA-PDT进行了视觉、组织学和分子评估。结果:联合用药能明显抑制uv - b诱导的皮肤病变的生长。TUNEL染色显示单药和联合治疗后细胞凋亡增加,Ki-67染色显示治疗区域角质细胞增殖减少,DNA损伤减轻。mRNA表达分析显示,凋亡相关基因(p16INK4a, p21CIP1)上调,抗肿瘤免疫反应(IL-6, IL-8)增强。值得注意的是,联合治疗增强了治疗效果,而应用顺序似乎与体内治疗效果无关。结论:总的来说,这些结果表明CAP可以增强传统ALA-PDT的抗肿瘤作用,支持先前对SCC细胞的研究结果。
Cold Atmospheric Plasma Improves the Therapeutic Success of Photodynamic Therapy on UV-B-Induced Squamous Cell Carcinoma in Hairless Mice.
Background/Objectives: Actinic keratosis (AK) occurs on sun-damaged skin and is considered a precursor to squamous cell carcinoma (SCC). Photodynamic therapy (PDT), using 5-aminolevulinic acid (ALA) and red light, is a common treatment for AK. However, its clinical efficacy for invasive tumors such as SCC is limited by the poor penetration and distribution of the photosensitizer. Cold atmospheric plasma (CAP), a partially ionized gas, increases skin permeability and exhibits anti-cancer properties through the generation of reactive oxygen species (ROS). In a previous study, CAP showed promising synergistic effects when combined with ALA-PDT for the treatment of SCC cells in vitro. The present study investigated the effects of combining CAP with ALA-PDT on cutaneous AK and SCC induced by ultraviolet B (UV-B) irradiation in SKH1 hairless mice. Methods: We compared various application sequences (CAP-ALA-red light, ALA-red light-CAP, and ALA-CAP-red light) against conventional ALA-PDT using visual, histological, and molecular assessments of the affected skin. Results: The results demonstrated that combined treatments strongly inhibited the growth of UV-B-induced skin lesions. TUNEL staining revealed increased apoptosis following both single and combined therapies, while Ki-67 staining indicated reduced keratinocyte proliferation and diminished DNA damage in treated areas. mRNA expression analysis showed the upregulation of apoptosis-related genes (p16INK4a, p21CIP1) alongside enhanced anti-tumor immune responses (IL-6, IL-8) in the affected tissue samples. Notably, the combined treatment enhances the therapeutic effect, whereas the sequence of application does not seem to be relevant for therapeutic efficacy in vivo. Conclusions: Overall, these results suggest that CAP may enhance the anti-tumor effect of conventional ALA-PDT, supporting previous findings on SCC cells.
PharmaceuticalsPharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍:
Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.