医学
前列腺癌
癌症
肿瘤科
内科学
癌症研究
生物信息学
生物
作者
Mitchell G. Lawrence,Renea A. Taylor,Georgia B. Cuffe,Lisa S. Ang,Ashlee K. Clark,David L. Goode,Laura H. Porter,Clémentine Le Magnen,Nora M. Navone,Jack A. Schalken,Yuzhuo Wang,Wytske M. van Weerden,Eva Corey,John T. Isaacs,Peter S. Nelson,Gail P. Risbridger
标识
DOI:10.1038/s41585-022-00706-x
摘要
Patient-derived xenografts (PDXs) are generated by engrafting human tumours into mice. Serially transplantable PDXs are used to study tumour biology and test therapeutics, linking the laboratory to the clinic. Although few prostate cancer PDXs are available in large repositories, over 330 prostate cancer PDXs have been established, spanning broad clinical stages, genotypes and phenotypes. Nevertheless, more PDXs are needed to reflect patient diversity, and to study new treatments and emerging mechanisms of resistance. We can maximize the use of PDXs by exchanging models and datasets, and by depositing PDXs into biorepositories, but we must address the impediments to accessing PDXs, such as institutional, ethical and legal agreements. Through collaboration, researchers will gain greater access to PDXs representing diverse features of prostate cancer. This Perspective covers existing patient-derived xenografts (PDXs) of prostate cancer, and their features and uses in basic and preclinical research. The authors also discuss the need for additional PDXs, and how collaboration in prostate cancer PDX research can be improved.
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