首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Metalloporphyrin Pd(T4) Exhibits Oncolytic Activity and Cumulative Effects with 5-ALA Photodynamic Treatment against C918 Cells
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Metalloporphyrin Pd(T4) Exhibits Oncolytic Activity and Cumulative Effects with 5-ALA Photodynamic Treatment against C918 Cells

机译:金属卟啉Pd(T4)表现出5-ALA光动力学处理对C918细胞的溶瘤活性和累积作用

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摘要

Photodynamic therapy is a non-invasive method where light activates a photosensitizer bound to cancer cells, generating reactive oxygen species and resulting in cell death. This study assessed the oncolytic potential of photodynamic therapy, comparing European Medicines Agency and United States Food and Drug Administration-approved 5-aminolevulinic acid (5-ALA) to a metalloporphyrin, Pd(T4), against a highly invasive uveal melanoma cell line (C918) in two- and three-dimensional models . Epithelial monolayer studies displayed strong oncolytic effects (>70%) when utilizing Pd(T4) at a fraction of the concentration, and reduced pre-illumination time compared to 5-ALA post-405 nm irradiance. When analyzed at sub-optimal concentrations, application of Pd(T4) and 5-ALA with 405 nm displayed cumulative effects. Lethality from Pd(T4)-photodynamic therapy was maintained within a three-dimensional model, including the more resilient vasculogenic mimicry-forming cells, though at lower rates. At high concentrations, modality of cell death exhibited necrosis partially dependent on reactive oxygen species. However, sub-optimal concentrations of photosensitizer exhibited an apoptotic protein expression profile characterized by increased Bax/Bcl-2 ratio and endoplasmic stress-related proteins, along with downregulation of apoptotic inhibitors CIAP-1 and -2. Together, our results indicate Pd(T4) as a strong photosensitizer alone and in combination with 5-ALA against C918 cells.
机译:光动力疗法是一种非侵入性方法,其中光激活与癌细胞结合的光敏剂,产生活性氧,导致细胞死亡。这项研究评估了光动力疗法的溶瘤潜能,将欧洲药物管理局和美国食品药品监督管理局批准的5-氨基乙酰丙酸(5-ALA)与金属卟啉Pd(T4)进行了比较,以针对高侵袭性葡萄膜黑色素瘤细胞系( C918)在二维和三维模型中。上皮单层研究显示,当使用浓度为Pd(T4)的一小部分时,其溶瘤作用强(> 70%),并且与405 nm后辐照的5-ALA相比,其照射前时间缩短。当在次优浓度下进行分析时,使用405 nm的Pd(T4)和5-ALA表现出累积效应。 Pd(T4)-光动力疗法的致死性在一个三维模型中得以维持,包括更具弹性的血管生成模拟物形成细胞,尽管其发生率较低。在高浓度下,细胞死亡的形态表现出坏死,部分取决于活性氧。然而,次佳浓度的光敏剂显示出凋亡蛋白表达特征,其特征在于增加的Bax / Bcl-2比和内质应激相关蛋白,以及凋亡抑制剂CIAP-1和-2的下调。总之,我们的结果表明,Pd(T4)单独用作强光敏剂,并与针对C918细胞的5-ALA结合使用。

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