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Gene and miRNA expression signature of Lewis lung carcinoma LLC1 cells in extracellular matrix enriched microenvironment

机译:富含细胞外基质的微环境中Lewis肺癌LLC1细胞的基因和miRNA表达特征

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摘要

BackgroundThe extracellular matrix (ECM), one of the key components of tumor microenvironment, has a tremendous impact on cancer development and highly influences tumor cell features. ECM affects vital cellular functions such as cell differentiation, migration, survival and proliferation. Gene and protein expression levels are regulated in cell-ECM interaction dependent manner as well. The rate of unsuccessful clinical trials, based on cell culture research models lacking the ECM microenvironment, indicates the need for alternative models and determines the shift to three-dimensional (3D) laminin rich ECM models, better simulating tissue organization. Recognized advantages of 3D models suggest the development of new anticancer treatment strategies. This is among the most promising directions of 3D cell cultures application. However, detailed analysis at the molecular level of 2D/3D cell cultures and tumors in vivo is still needed to elucidate cellular pathways most promising for the development of targeted therapies. In order to elucidate which biological pathways are altered during microenvironmental shift we have analyzed whole genome mRNA and miRNA expression differences in LLC1 cells cultured in 2D or 3D culture conditions.
机译:背景细胞外基质(ECM)是肿瘤微环境的关键组成部分之一,对癌症的发展具有巨大的影响,并高度影响肿瘤细胞的功能。 ECM影响重要的细胞功能,例如细胞分化,迁移,存活和增殖。基因和蛋白质表达水平也以细胞-ECM相互作用依赖性方式调节。基于缺乏ECM微环境的细胞培养研究模型,临床试验的失败率表明了对替代模型的需求,并确定了向富含三维(3D)层粘连蛋白的ECM模型的转移,从而更好地模拟了组织组织。 3D模型的公认优势表明开发了新的抗癌治疗策略。这是3D细胞培养应用最有希望的方向之一。但是,仍需要在体内2D / 3D细胞培养物和肿瘤的分子水平上进行详细分析,以阐明最有希望用于靶向疗法发展的细胞途径。为了阐明微环境转移过程中哪些生物学途径被改变,我们分析了在2D或3D培养条件下培养的LLC1细胞中的全基因组mRNA和miRNA表达差异。

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