The future of patient-derived xenografts in prostate cancer research

被引:0
|
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
机构
[1] Monash University,Department of Anatomy and Developmental Biology
[2] Monash Biomedicine Discovery Institute,Melbourne Urological Research Alliance
[3] Peter MacCallum Cancer Centre,Sir Peter MacCallum Department of Oncology
[4] The University of Melbourne,Department of Physiology
[5] Cabrini Institute,Divisions of Human Biology and Clinical Research
[6] Cabrini Health,Department of Urology
[7] Monash University,Institute of Medical Genetics and Pathology
[8] Fred Hutchinson Cancer Research Center,Department of Urology
[9] Radboud University Medical Center,Department of Biomedicine
[10] University Hospital Basel,Department of Genitourinary Medical Oncology
[11] University Hospital Basel,David H. Koch Center for Applied Research of Genitourinary Cancers
[12] University Hospital Basel,Department of Urologic Sciences, Faculty of Medicine
[13] University of Basel,Department of Experimental Therapeutics
[14] The University of Texas MD Anderson Cancer Center,Department of Urology
[15] The University of Texas MD Anderson Cancer Center,Department of Urology
[16] Vancouver Prostate Centre,Department of Oncology, Sidney Kimmel Comprehensive Cancer Center (SKCCC)
[17] University of British Columbia,Department of Pharmacology and Molecular Science
[18] BC Cancer Agency,Department of Urology, James Buchanan Brady Urological Institute
[19] Erasmus MC Cancer Institute,undefined
[20] University of Washington,undefined
[21] Johns Hopkins University School of Medicine,undefined
[22] Johns Hopkins University School of Medicine,undefined
[23] Johns Hopkins University School of Medicine,undefined
来源
Nature Reviews Urology | 2023年 / 20卷
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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.
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页码:371 / 384
页数:13
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