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A spheroid-based 3-D culture model for pancreatic cancer drug testing, using the acid phosphatase assay

机译:使用酸性磷酸酶测定法的基于球体的3-D培养模型用于胰腺癌药物测试

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Current therapy for pancreatic cancer is multimodal, involving surgery and chemotherapy. However, development of pancreatic cancer therapies requires a thorough evaluation of drug efficacy in vitro before animal testing and subsequent clinical trials. Compared to two-dimensional culture of cell monolayer, three-dimensional (3-D) models more closely mimic native tissues, since the tumor microenvironment established in 3-D models often plays a significant role in cancer progression and cellular responses to the drugs. Accumulating evidence has highlighted the benefits of 3-D in vitro models of various cancers. In the present study, we have developed a spheroid-based, 3-D culture of pancreatic cancer cell lines MIAPaCa-2 and PANC-1 for pancreatic drug testing, using the acid phosphatase assay. Drug efficacy testing showed that spheroids had much higher drug resistance than monolayers. This model, which is characteristically reproducible and easy and offers rapid handling, is the preferred choice for filling the gap between monolayer cell cultures and in vivo models in the process of drug development and testing for pancreatic cancer.
机译:当前胰腺癌的治疗是多模式的,涉及手术和化学疗法。然而,胰腺癌疗法的发展需要在动物试验和后续临床试验之前,在体外对药物功效进行全面评估。与二维细胞单层培养相比,三维(3-D)模型更接近于模拟天然组织,因为在3-D模型中建立的肿瘤微环境通常在癌症进展和对药物的细胞反应中起重要作用。越来越多的证据突出了各种癌症的3-D体外模型的好处。在本研究中,我们使用酸性磷酸酶测定法开发了基于球体的胰腺癌细胞系MIAPaCa-2和PANC-1的3-D培养物。药物功效测试表明,类球体比单层具有更高的耐药性。该模型具有典型的可复制性且易于操作,并提供快速的处理方法,是填补单层细胞培养物与体内模型在胰腺癌药物开发和测试过程中的空白的首选。

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