Evaluation of the antineoplastic properties of the photosensitizer biscyanine in 2D and 3D tumor cell models and artificial skin models

IF 3.9 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of photochemistry and photobiology. B, Biology Pub Date : 2025-01-01 DOI:10.1016/j.jphotobiol.2024.113078
Pedro Victor Silva Resende , Izabela Natália Faria Gomes , Maria Clara Peixoto , Giulia Rodrigues Stringhetta , Lidia Maria Rebolho Batista Arantes , Vladimir Alexandrovich Kuzmin , Iouri Borissevitch , Rui Manuel Reis , Vinícius de Lima Vazquez , Lucimara Perpetua Ferreira , Renato José Silva Oliveira
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Abstract

Background

Photodynamic Therapy (PDT) is a therapeutic modality that combines the application of a photoactive compound (photosensitizer, PS) with low-power light to generate reactive oxygen species in the target tissue, resulting in cytotoxic damage and cell death, while sparing adjacent tissues. The objective of this study was to evaluate the phototoxicity of a cyanine dye with two chromophores (biscyanines, BCD) in systems with varying levels of cellular organization, and we used the Photogem® (a photosensitizer approved by the Brazilian ANVISA agency for clinical use in Photodynamic Therapy) as a positive control.

Materials and methods

The cytotoxicity of the compounds was assessed in vitro in 2D monolayers, 3D spheroid cultures, and artificial skin models. Four tumoral cell lines A375 (melanoma), HCB-541 (cutaneous squamous cell carcinoma), Vu120T and Vu147T (head and neck cancer), and two normal cell lines fibroblastic HFF-1 and keratinocyte HACAT were used in this study. Cell viability, migration, production of reactive oxygen species, expression of proteins linked to DNA damage and repair, internalization, and skin permeation of PS agents.

Results

Light irradiation in the presence of the PS resulted in greater cytotoxic effects for BCD as compared to Photogem®, which was accompanied by an increase in the production of reactive oxygen species including H2O2, elevated levels of cleaved PARP, and a higher rate of phosphorylated H2AX protein. BCD demonstrated enhanced internalization and bioaccumulation in the spheroids and equivalent skin models.

Conclusion

BCD, as a photosensitizer, showed higher cytotoxicity, with an increased ability to generate reactive oxygen species. This led to reduced cell viability, inhibited migration, and upregulated DNA damage-related proteins. Additionally, its enhanced cellular uptake improved skin barrier permeability, making BCD a strong candidate for in vivo Photodynamic Therapy.

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在二维和三维肿瘤细胞模型及人造皮肤模型中评估光敏剂双氰胺的抗肿瘤特性。
背景:光动力疗法(PDT)是一种结合应用光活性化合物(光敏剂,PS)和低功率光在靶组织中产生活性氧的治疗方式,导致细胞毒性损伤和细胞死亡,同时保留邻近组织。本研究的目的是评估具有两种发色团(双花青素,BCD)的花青素染料在不同细胞组织水平的系统中的光毒性,我们使用photogm®(巴西ANVISA机构批准用于临床光动力治疗的光敏剂)作为阳性对照。材料和方法:采用体外二维单层、三维球形培养和人造皮肤模型对化合物的细胞毒性进行了评估。本研究使用4种肿瘤细胞系A375(黑色素瘤)、HCB-541(皮肤鳞状细胞癌)、Vu120T和Vu147T(头颈部癌),以及2种正常细胞系成纤维细胞HFF-1和角化细胞HACAT。细胞活力、迁移、活性氧的产生、与DNA损伤和修复相关的蛋白质的表达、内化和PS剂的皮肤渗透。结果:与phogome®相比,PS存在下的光照射导致BCD的细胞毒性作用更大,这伴随着活性氧(包括H2O2)的产生增加,裂解PARP水平升高,以及更高的H2AX蛋白磷酸化率。BCD在球体和等效皮肤模型中表现出增强的内化和生物蓄积。结论:BCD作为光敏剂具有较高的细胞毒性,其产生活性氧的能力增强。这导致细胞活力降低,迁移受到抑制,DNA损伤相关蛋白上调。此外,其增强的细胞摄取改善了皮肤屏障的渗透性,使BCD成为体内光动力治疗的有力候选者。
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来源期刊
CiteScore
12.10
自引率
1.90%
发文量
161
审稿时长
37 days
期刊介绍: The Journal of Photochemistry and Photobiology B: Biology provides a forum for the publication of papers relating to the various aspects of photobiology, as well as a means for communication in this multidisciplinary field. The scope includes: - Bioluminescence - Chronobiology - DNA repair - Environmental photobiology - Nanotechnology in photobiology - Photocarcinogenesis - Photochemistry of biomolecules - Photodynamic therapy - Photomedicine - Photomorphogenesis - Photomovement - Photoreception - Photosensitization - Photosynthesis - Phototechnology - Spectroscopy of biological systems - UV and visible radiation effects and vision.
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