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Alterations in dysadherin expression and F-actin reorganization: a possible mechanism of hypericin-mediated photodynamic therapy in colon adenocarcinoma cells

机译:dysadherin表达和F-肌动蛋白重组的改变:金丝桃素介导的光动力疗法在结肠腺癌细胞中的可能机制

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Dysadherin is a recently found anti-adhesion molecule, therefore detection and down regulation of its expression is promising in cancer treatment. The up-regulation of dysadherin contributes to colon cancer recurrence and metastasis. Dysadherin also has connections with cytoskeletal proteins and it can cause alterations in the organisation of filamentous actin (F-actin) in metastatic cancers. In this study, hypericin (HYP)-mediated photodynamic therapy (PDT) was performed in two different grade colon adenocarcinoma cell lines HT-29 (Grade I) and Caco-2 (Grade II). Cells were treated with 0.04, 0.08 or 0.15?μM HYP concentrations and irradiated with (4?J/cm2) fluorescent lamps. The effects of HYP was examined 16 and 24?h after the activation. We investigated for the first time the effect of HYP-mediated PDT on the expression of dysadherin and F-actin organisation. According to the results, HYP mediated PDT caused a decrease in gene expression and immunofluorescence staining of dysadherin and an increase in actin stress fibers and actin aggregates in HT-29 and Caco-2 cell lines. Besides, cytotoxicity, number of floating cells and apoptotic index changed depending on the cell type, HYP concentration and incubation time. We have demonstrated for the first time that dysadherin and F-actin could be target molecules for HYP-mediated PDT in HT-29 and Caco-2 colon cancer cell lines.
机译:dysadherin是最近发现的一种抗粘附分子,因此在癌症治疗中检测和下调其表达是有希望的。 dysadherin的上调有助于结肠癌的复发和转移。 dysadherin还与细胞骨架蛋白有联系,它可以在转移性癌症中引起丝状肌动蛋白(F-actin)组织的改变。在这项研究中,金丝桃素(HYP)介导的光动力疗法(PDT)在两种不同等级的结肠腺癌细胞系HT-29(I级)和Caco-2(II级)中进行。用0.04、0.08或0.15?M HYP浓度处理细胞,并用(4?J / cm2)荧光灯照射。激活后16和24小时检查HYP的作用。我们首次研究了HYP介导的PDT对dysadherin和F-actin组织表达的影响。根据结果​​,HYP介导的PDT导致dysadherin的基因表达下降和免疫荧光染色,并且HT-29和Caco-2细胞系的肌动蛋白应激纤维和肌动蛋白聚集体增加。此外,细胞毒性,漂浮细胞数和凋亡指数还取决于细胞类型,HYP浓度和孵育时间。我们首次证明,dysadherin和F-actin可能是HT-29和Caco-2结肠癌细胞系中HYP介导的PDT的靶分子。

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