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Co-expression of autophagic markers following photodynamic therapy in SW620 human colon adenocarcinoma cells

机译:光动力学治疗后SW620人结肠腺癌细胞中自噬标志物的共表达

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Photodynamic therapy (PDT) is a minimally invasive cancer treatment. It involves the combination of a photosensitizer and light of a specific wavelength to generate singlet oxygen and other reactive oxygen species that lead to tumor cell death. Autophagy is one of the pathways that tumor cells undergo during photodamage and it is common in photodynamic therapy. The aim of this study was to examine the effect of in vitro PDT on the expression of autophagy-related proteins, autophagy related 7 (Atg7), light chain 3 (LC3) and Beclin-1. Human SW620 colon carcinoma cells were treated with 5-aminolevulinic acid (ALA)-based PDT at a dose of 3 mM. The irradiation was performed using 4.5 J/cm(2) total light and a fluence rate of 60 mW/cm(2). Autophagy was evaluated by immunocytochemistry using specific antibodies to Atg7, Beclin-1 and LC3. The evaluation was repeated at several time points (0, 4, 8 and 24 h) following irradiation. The induction of autophagy was observed directly following the 5-ALA-mediated PDT procedure with the strongest expression of autophagy-related proteins at 4 and 8 h after irradiation as demonstrated using immunocytochemistry. It was characterized by significantly increased expression of Beclin-1, Atg7 and LC3. To the best of our knowledge this is the first study to analyze Beclin-1, Atg7 and LC3 expression in a PDT-related experiment. This study enhances the understanding of the role of autophagy in PDT, which may contribute to better and more effective tumor responses to this therapy.
机译:光动力疗法(PDT)是一种微创癌症疗法。它涉及光敏剂和特定波长的光的组合,以产生单线态氧和其他可导致肿瘤细胞死亡的活性氧。自噬是肿瘤细胞在光损伤过程中经历的途径之一,在光动力疗法中很常见。这项研究的目的是检查体外PDT对自噬相关蛋白,自噬相关7(Atg7),轻链3(LC3)和Beclin-1表达的影响。用基于5-氨基乙酰丙酸(ALA)的PDT以3 mM的剂量处理人SW620结肠癌细胞。使用4.5 J / cm(2)的总光和60 mW / cm(2)的能量密度进行照射。使用针对Atg7,Beclin-1和LC3的特异性抗体通过免疫细胞化学评估自噬。辐照后的几个时间点(0、4、8和24小时)重复进行评估。如免疫细胞化学所示,在5-ALA介导的PDT程序后,直接观察到自噬的诱导,自噬相关蛋白的最强表达在照射后4和8 h。它的特征是Beclin-1,Atg7和LC3的表达明显增加。据我们所知,这是第一项在与PDT相关的实验中分析Beclin-1,Atg7和LC3表达的研究。这项研究增进了对自噬在PDT中作用的认识,这可能有助于更好地,更有效地对此疗法产生肿瘤反应。

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