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Simulating tumor microenvironment: changes in protein expression in an in vitro co-culture system

机译:模拟肿瘤微环境:体外共培养系统中蛋白质表达的变化

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The role of the microenvironment during the initiation and progression of carcinogenesis is thought to be of critical importance, both for the enhanced understanding of fundamental cancer biology as well as for improving molecular diagnostics and therapeutics. The aim of this study was to establish an in vitro model based on a co-culture of healthy human fibroblasts (HFs) and human osteosarcoma cells (MG-63s) to simulate the microenvironment including tumor and healthy cells. The HFs and MG-63s were in vitro co-cultured for a period of time ranging from 24 h to 7 days. Cell morphology and organization were studied using phase contrast microscopy while the expression of Human Cartilage Glycoprotein 39 (YKL-40), Vascular Endothelial Growth Factor (VEGF) and Matrix Metalloprotease 1 (MMP1) was investigated by Real Time PCR and Western Blotting. The results showed a characteristic disposition of tumor and healthy co-cultured cells in columns which are not visible in tumor and healthy cells grown singularly. The expression of YKL-40, VEGF and MMP1 significantly changed in co-cultured cells compared to HFs and MG-63s separately cultured. We concluded that the tumor microenvironment has an influence on the protein expression of the healthy surrounding tissues and the process of tumorigenicity.
机译:人们认为,微环境在致癌作用的开始和发展过程中的作用至关重要,这对于增强对基础癌症生物学的认识以及改善分子诊断和治疗方法都是至关重要的。这项研究的目的是建立基于健康人类成纤维细胞(HFs)和人类骨肉瘤细胞(MG-63s)共同培养的体外模型,以模拟包括肿瘤和健康细胞在内的微环境。将HF和MG-63进行体外共培养24小时至7天。使用相差显微镜研究细胞形态和组织,同时通过实时荧光定量PCR和Western Blotting研究人软骨糖蛋白39(YKL-40),血管内皮生长因子(VEGF)和基质金属蛋白酶1(MMP1)的表达。结果显示了肿瘤和健康共培养细胞在柱子中的特征分布,这在单独生长的肿瘤和健康细胞中不可见。与分别培养的HF和MG-63相比,在共培养的细胞中YKL-40,VEGF和MMP1的表达发生了显着变化。我们得出的结论是,肿瘤微环境对健康的周围组织的蛋白质表达和致瘤性过程有影响。

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