Organoids: An Emerging Precision Medicine Model for Prostate Cancer Research

被引:8
作者
Waseem, Mohammad [1 ]
Wang, Bi-Dar [1 ,2 ]
机构
[1] Univ Maryland Eastern Shore, Sch Pharm & Hlth Profess, Dept Pharmaceut Sci, Princess Anne, MD 21853 USA
[2] Univ Maryland, Greenebaum Comprehens Canc Ctr, Hormone Related Canc Program, Baltimore, MD 21201 USA
关键词
prostate cancer; organoids; 3D model; precision medicine; in vitro and in vivo models; castration resistant prostate cancer (CRPC); neuroendocrine prostate cancer (NEPC); IN-VITRO; ANTIANDROGEN RESISTANCE; TUMOR MICROENVIRONMENT; ANDROGEN DEPRIVATION; LINEAGE PLASTICITY; COLORECTAL-CANCER; DNA METHYLATION; CELLS; THERAPY; DIFFERENTIATION;
D O I
10.3390/ijms25021093
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prostate cancer (PCa) has been known as the most prevalent cancer disease and the second leading cause of cancer mortality in men almost all over the globe. There is an urgent need for establishment of PCa models that can recapitulate the progress of genomic landscapes and molecular alterations during development and progression of this disease. Notably, several organoid models have been developed for assessing the complex interaction between PCa and its surrounding microenvironment. In recent years, PCa organoids have been emerged as powerful in vitro 3D model systems that recapitulate the molecular features (such as genomic/epigenomic changes and tumor microenvironment) of PCa metastatic tumors. In addition, application of organoid technology in mechanistic studies (i.e., for understanding cellular/subcellular and molecular alterations) and translational medicine has been recognized as a promising approach for facilitating the development of potential biomarkers and novel therapeutic strategies. In this review, we summarize the application of PCa organoids in the high-throughput screening and establishment of relevant xenografts for developing novel therapeutics for metastatic, castration resistant, and neuroendocrine PCa. These organoid-based studies are expected to expand our knowledge from basic research to clinical applications for PCa diseases. Furthermore, we also highlight the optimization of PCa cultures and establishment of promising 3D organoid models for in vitro and in vivo investigations, ultimately facilitating mechanistic studies and development of novel clinical diagnosis/prognosis and therapies for PCa.
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页数:23
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