Khorsandi Khatereh, Hosseinzadeh Reza, Chamani Elham
Department of Photodynamic, Medical Laser Research Center, Yara Institute, ACECR, Tehran, Iran.
Department of Medical Laser, Medical Laser Research Center, Yara Institute, ACECR, Tehran, Iran.
Cancer Cell Int. 2020 Oct 29;20:525. doi: 10.1186/s12935-020-01616-x. eCollection 2020.
Melanoma as a type of skin cancer, is associated with a high mortality rate. Therefore, early diagnosis and efficient surgical treatment of this disease is very important. Photodynamic therapy (PDT) involves the activation of a photosensitizer by light at specific wavelength that interacts with oxygen and creates singlet oxygen molecules or reactive oxygen species (ROS), which can lead to tumor cell death. Furthermore, one of the main approches in the prevention and treatment of various cancers is plant compounds application. Phenolic compounds are essential class of natural antioxidants, which play crucial biological roles such as anticancer effects. It was previously suggested that flavonoid such as rutoside could acts as pro-oxidant or antioxidant. Hence, in this study, we aimed to investigate the effect of rutoside on the combination therapy with methylene blue (MB) assisted by photodynamic treatment (PDT) using red light source (660 nm; power density: 30 mW/cm) on A375 human melanoma cancer cells.
For this purpose, the A375 human melanoma cancer cell lines were treated by MB-PDT and rutoside. Clonogenic cell survival, MTT assay, and cell death mechanisms were also determined after performing the treatment. Subsequently, after the rutoside treatment and photodynamic therapy (PDT), cell cycle and intracellular reactive oxygen species (ROS) generation were measured.
The obtained results showed that, MB-PDT and rutoside had better cytotoxic and antiprolifrative effects on A375 melanoma cancer cells compared to each free drug, whereas the cytotoxic effect on HDF human dermal fibroblast cell was not significant. MB-PDT and rutoside combination induced apoptosis and cell cycle arrest in the human melanoma cancer cell line. Intracellular ROS increased in A375 cancer cell line after the treatment with MB-PDT and rutoside.
The results suggest that, MB-PDT and rutoside could be considered as novel approaches as the combination treatment of melanoma cancer.
黑色素瘤作为一种皮肤癌,死亡率很高。因此,对该疾病进行早期诊断和有效的手术治疗非常重要。光动力疗法(PDT)涉及通过特定波长的光激活光敏剂,该光敏剂与氧气相互作用并产生单线态氧分子或活性氧(ROS),这可导致肿瘤细胞死亡。此外,植物化合物的应用是预防和治疗各种癌症的主要方法之一。酚类化合物是天然抗氧化剂的重要类别,具有抗癌等关键生物学作用。先前有研究表明,芦丁等黄酮类化合物可作为促氧化剂或抗氧化剂。因此,在本研究中,我们旨在研究芦丁对使用红色光源(660 nm;功率密度:30 mW/cm)的光动力治疗(PDT)辅助亚甲蓝(MB)联合治疗A375人黑色素瘤癌细胞的影响。
为此,用MB-PDT和芦丁处理A375人黑色素瘤癌细胞系。处理后还测定了克隆形成细胞存活率、MTT法和细胞死亡机制。随后,在芦丁处理和光动力疗法(PDT)后,测量细胞周期和细胞内活性氧(ROS)的产生。
所得结果表明,与每种游离药物相比,MB-PDT和芦丁对A375黑色素瘤癌细胞具有更好的细胞毒性和抗增殖作用,而对人皮肤成纤维细胞(HDF)的细胞毒性作用不显著。MB-PDT与芦丁联合诱导人黑色素瘤癌细胞系凋亡和细胞周期停滞。用MB-PDT和芦丁处理后,A375癌细胞系中的细胞内ROS增加。
结果表明,MB-PDT和芦丁可被视为黑色素瘤联合治疗的新方法。