School of Biomedical Sciences, Faculty of Health, Queensland University of Technology (QUT) at Translational Research Institute; Queensland Bladder Cancer Initiative (QBCI); Centre for Personalised Analysis of Cancers (CPAC); Australian Prostate Cancer Research Centre - Queensland.
School of Biomedical Sciences, Faculty of Health, Queensland University of Technology (QUT) at Translational Research Institute; Queensland Bladder Cancer Initiative (QBCI); Centre for Personalised Analysis of Cancers (CPAC); Australian Prostate Cancer Research Centre - Queensland; Department of Urology, Princess Alexandra Hospital.
J Vis Exp. 2021 Dec 28(178). doi: 10.3791/63192.
Current in vitro therapeutic testing platforms lack relevance to tumor pathophysiology, typically employing cancer cell lines established as two-dimensional (2D) cultures on tissue culture plastic. There is a critical need for more representative models of tumor complexity that can accurately predict therapeutic response and sensitivity. The development of three-dimensional (3D) ex vivo culture of patient-derived organoids (PDOs), derived from fresh tumor tissues, aims to address these shortcomings. Organoid cultures can be used as tumor surrogates in parallel to routine clinical management to inform therapeutic decisions by identifying potential effective interventions and indicating therapies that may be futile. Here, this procedure aims to describe strategies and a detailed step-by-step protocol to establish bladder cancer PDOs from fresh, viable clinical tissue. Our well-established, optimized protocols are practical to set up 3D cultures for experiments using limited and diverse starting material directly from patients or patient-derived xenograft (PDX) tumor material. This procedure can also be employed by most laboratories equipped with standard tissue culture equipment. The organoids generated using this protocol can be used as ex vivo surrogates to understand both the molecular mechanisms underpinning urological cancer pathology and to evaluate treatments to inform clinical management.
目前的体外治疗测试平台与肿瘤病理生理学缺乏相关性,通常采用二维(2D)培养在组织培养塑料上建立的癌细胞系。迫切需要更具代表性的肿瘤复杂性模型,以准确预测治疗反应和敏感性。从新鲜肿瘤组织中衍生的患者来源类器官(PDO)的三维(3D)体外培养的发展旨在解决这些缺点。类器官培养物可以作为肿瘤替代物与常规临床管理并行使用,通过确定潜在的有效干预措施并指示可能无效的治疗方法来告知治疗决策。在这里,本程序旨在描述从新鲜、有活力的临床组织中建立膀胱癌 PDO 的策略和详细的分步协议。我们建立的经过良好验证的优化方案,可用于使用直接从患者或患者衍生的异种移植(PDX)肿瘤材料中获得的有限且多样化的起始材料设置 3D 培养物进行实验。配备标准组织培养设备的大多数实验室也可以采用此程序。使用该方案生成的类器官可作为体外替代品,用于了解泌尿外科癌症病理学的分子机制,并评估治疗方法以告知临床管理。