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Defining the challenges and opportunities for using patient‐derived models in prostate cancer research

前列腺癌 转化研究 标准化 癌症 医学 前列腺 多样性(控制论) 医学物理学 计算机科学 数据科学 病理 内科学 人工智能 操作系统
作者
W. Nathaniel Brennen,Clémentine Le Magnen,Sofia Karkampouna,Nicolás Anselmino,Nathalie Bock,Nicholas Choo,Ashlee K. Clark,Ilsa M. Coleman,R. Dolgos,Alison Ferguson,David L. Goode,Marianna Krutihof‐de Julio,Nora M. Navone,Peter S. Nelson,Edward O’Neill,Laura H. Porter,Weranja Ranasinghe,Takuro Sunada,Elizabeth D. Williams,Lisa M. Butler
出处
期刊:The Prostate [Wiley]
卷期号:84 (7): 623-635 被引量:1
标识
DOI:10.1002/pros.24682
摘要

Abstract Background There are relatively few widely used models of prostate cancer compared to other common malignancies. This impedes translational prostate cancer research because the range of models does not reflect the diversity of disease seen in clinical practice. In response to this challenge, research laboratories around the world have been developing new patient‐derived models of prostate cancer, including xenografts, organoids, and tumor explants. Methods In May 2023, we held a workshop at the Monash University Prato Campus for researchers with expertise in establishing and using a variety of patient‐derived models of prostate cancer. This review summarizes our collective ideas on how patient‐derived models are currently being used, the common challenges, and future opportunities for maximizing their usefulness in prostate cancer research. Results An increasing number of patient‐derived models for prostate cancer are being developed. Despite their individual limitations and varying success rates, these models are valuable resources for exploring new concepts in prostate cancer biology and for preclinical testing of potential treatments. Here we focus on the need for larger collections of models that represent the changing treatment landscape of prostate cancer, robust readouts for preclinical testing, improved in vitro culture conditions, and integration of the tumor microenvironment. Additional priorities include ensuring model reproducibility, standardization, and replication, and streamlining the exchange of models and data sets among research groups. Conclusions There are several opportunities to maximize the impact of patient‐derived models on prostate cancer research. We must develop large, diverse and accessible cohorts of models and more sophisticated methods for emulating the intricacy of patient tumors. In this way, we can use the samples that are generously donated by patients to advance the outcomes of patients in the future.
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