首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Novel Insights into the Effect of Hyperforin and Photodynamic Therapy with Hypericin on Chosen Angiogenic Factors in Colorectal Micro-Tumors Created on Chorioallantoic Membrane
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Novel Insights into the Effect of Hyperforin and Photodynamic Therapy with Hypericin on Chosen Angiogenic Factors in Colorectal Micro-Tumors Created on Chorioallantoic Membrane

机译:Hyperforin和金丝桃素光动力疗法对绒毛膜尿囊膜上结直肠微肿瘤中所选血管生成因子的影响的新见解。

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摘要

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.
机译:金丝桃素(HY-PDT)和金丝桃素(HP)的光动力疗法可能是结直肠癌(CRC)的治疗方式,但缺少其对CRC中血管生成因子影响的证据。便利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细胞模型和微肿瘤进行了比较。通过组织学分析确定微肿瘤的程度以及与绒膜尿囊膜(CAM)的相互关系。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。通过比色测定法评估代谢活性状态以评估细胞代谢活性(MTT测定),并通过流式细胞术确定HY积累。通过Western印迹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,并表明它们的作用受实验模型的结构特征影响。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的影响的方法。尽管HY-PDT和HP对CRC有抑制作用,但仍观察到某些促血管生成因子的表达增加。我们还表明,在鹌鹑CAM上创建的CRC实验性微肿瘤可用于分析基因和蛋白质表达。

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