类有机物
离体
膀胱癌
医学
精密医学
癌症
协议(科学)
体内
病理
计算机科学
计算生物学
生物信息学
癌症研究
生物
神经科学
内科学
生物技术
替代医学
作者
Patrick B. Thomas,Mahasha P. J. Perera,Saeid Alinezhad,Andre Joshi,Paria Saadat,Clarissa Nicholls,Caitlin P. Devonport,Alivia R. Calabrese,Abby R. Templeton,Jack R. Wood,Nathan J. Mackenzie,Penny L. Jeffery,Ian Vela,Elizabeth D. Williams
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI