Institute of Biology and Ecology, Faculty of Science, Pavol Jozef Šafárik University in Košice, Šrobárova 2, 041 54 Košice, Slovakia.
Cancer Research Institute BMC, Slovak Academy of Sciences, Dúbravská cesta 9, 845 05 Bratislava, Slovakia.
Int J Mol Sci. 2019 Jun 19;20(12):3004. doi: 10.3390/ijms20123004.
Photodynamic therapy with hypericin (HY-PDT) and hyperforin (HP) could be treatment modalities for colorectal cancer (CRC), but evidence of their effect on angiogenic factors in CRC is missing. Convenient experimental model utilization is essential for angiogenesis research. Therefore, not only 2D cell models, but also 3D cell models and micro-tumors were used and compared. The micro-tumor extent and interconnection with the chorioallantoic membrane (CAM) was determined by histological analyses. The presence of proliferating cells and HY penetration into the tumor mass were detected by fluorescence microscopy. The metabolic activity status was assessed by an colorimetric assay for assessing cell metabolic activity (MTT assay) and HY accumulation was determined by flow cytometry. Pro-angiogenic factor expression was determined by Western blot and quantitative real-time polymerase chain reaction (RT-qPCR). We confirmed the cytotoxic effect of HY-PDT and HP and showed that their effect is influenced by structural characteristics of the experimental model. We have pioneered a method for analyzing the effect of HP and cellular targeted HY-PDT on pro-angiogenic factor expression in CRC micro-tumors. Despite the inhibitory effect of HY-PDT and HP on CRC, the increased expression of some pro-angiogenic factors was observed. We also showed that CRC experimental micro-tumors created on quail CAM could be utilized for analyses of gene and protein expression.
血卟啉(HY-PDT)和贯叶连翘素(HP)的光动力疗法可能是结直肠癌(CRC)的治疗方法,但缺乏它们对 CRC 血管生成因子影响的证据。方便的实验模型利用对于血管生成研究至关重要。因此,不仅使用了 2D 细胞模型,还使用了 3D 细胞模型和微肿瘤,并进行了比较。通过组织学分析确定微肿瘤的范围及其与绒毛尿囊膜(CAM)的连接。通过荧光显微镜检测增殖细胞的存在和 HY 渗透到肿瘤块中。通过用于评估细胞代谢活性的比色法测定(MTT 测定)和通过流式细胞术测定 HY 积累来评估代谢活性状态。通过 Western blot 和定量实时聚合酶链反应(RT-qPCR)确定促血管生成因子的表达。我们证实了 HY-PDT 和 HP 的细胞毒性作用,并表明其作用受实验模型结构特征的影响。我们开创了一种分析 HP 和细胞靶向 HY-PDT 对 CRC 微肿瘤中促血管生成因子表达影响的方法。尽管 HY-PDT 和 HP 对 CRC 具有抑制作用,但观察到一些促血管生成因子的表达增加。我们还表明,可以在鹌鹑 CAM 上创建的 CRC 实验性微肿瘤用于分析基因和蛋白质表达。