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首页> 外文期刊>Journal of biomolecular screening: The official journal of the Society for Biomolecular Screening >A more aggressive breast cancer spheroid model coupled to an electronic capillary sensor system for a high-content screening of cytotoxic agents in cancer therapy: 3-dimensional in vitro tumor spheroids as a screening model
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A more aggressive breast cancer spheroid model coupled to an electronic capillary sensor system for a high-content screening of cytotoxic agents in cancer therapy: 3-dimensional in vitro tumor spheroids as a screening model

机译:与电子毛细管传感器系统耦合的更具侵略性的乳腺癌球体模型,用于癌症治疗中细胞毒素剂的高含量筛选:3维体外肿瘤球体作为筛选模型

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摘要

One major problem in cancer therapy is the immortality of tumor cells showing an active telomerase, which is responsible for the elongation of the telomeres after each cellular division and the knocking down of apoptotic suppressors. A further phenomenon occurring during cancer therapies is the problem of multicellular resistance. To develop therapeutic anticancer approaches inducing cellular apoptosis, gene-modified biological in vitro systems were established and evaluated for drug, screening in a capillary system for a real-time, impedimertic monitoring. Multicellular spheroids of the human breast cancer cell line T-47D clone II were transfected with 1) antisense caspase-3 cDNA expression vectors for knocking down the main cell death molecule and 2) sense Bel-xi cDNA expression vectors for overexpressing the apoptotic suppressor, resulting in more aggressive tumor models. These gene-modified tumor spheroids less sensitive for apoptosis were developed for screening drugs such as methotrexate in tumor spheroid-based biosensor systems via impedance spectroscopy. In this report, it is demonstrated that this could successfully exhibit that this real-time monitoring system with tumor spheroids positioned in a capillary system with a 4-electrode configuration is the most efficient high-content screening module for impedimetric measurements of physiological alterations during gene modification and drug application.
机译:癌症治疗中的一个主要问题是显示活性端粒酶的肿瘤细胞的永生性,其导致每次细胞分裂后端粒的延长和凋亡抑制子的敲除。在癌症治疗期间发生的另一现象是多细胞抗性问题。为了开发诱导细胞凋亡的治疗性抗癌方法,建立了基因修饰的生物体外系统,并对其药物进行了评估,并在毛细血管系统中进行筛查,以进行实时,阻抗监测。用1)用于敲低主要细胞死亡分子的反义caspase-3 cDNA表达载体和2)用于过表达凋亡抑制子的有义Bel-xi cDNA表达载体转染人类乳腺癌细胞T-47D克隆II的多细胞球体。导致更具侵略性的肿瘤模型。这些对细胞凋亡不那么敏感的基因修饰的肿瘤球被开发用于通过阻抗谱法在基于肿瘤球的生物传感器系统中筛选诸如甲氨蝶呤的药物。在本报告中,证明了这可以成功地展示出这种实时监测系统,其中肿瘤球体位于具有4电极配置的毛细管系统中,是用于阻抗测量基因过程中生理变化的最有效的高内涵筛选模块修饰和药物应用。

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