Patient-derived organoid co-culture systems as next-generation models for bladder cancer stem cell research

被引:0
作者
Yang, Ruici [1 ,2 ]
Wang, Shanzhao [1 ]
Li, Zhichao [1 ]
Yin, Cong [1 ]
Huang, Wei [3 ]
Huang, Weiren [1 ,2 ]
机构
[1] Shenzhen Univ, Shenzhen Peoples Hosp 2, Affiliated Hosp 1, Inst Adv Study,Int Canc Ctr,Synthet Biol Res Ctr,M, Shenzhen 518060, Peoples R China
[2] Chinese Acad Sci, Shenzhen Inst Synthet Biol, Shenzhen Inst Adv Technol, Shenzhen Key Lab Synthet Genom,Guangdong Prov Key, Shenzhen 518055, Peoples R China
[3] Southern Univ Sci & Technol, Dept Biol, Shenzhen 518055, Peoples R China
关键词
Bladder cancer; Cancer stem cell; Patient derived organoid co-culture systems; Tumor microenvironment; IN-VITRO; LUMINAL SUBTYPES; DIFFERENTIATION; PROGRESSION; BASAL; DRUG; CHEMOTHERAPY; CISPLATIN; EVOLUTION; ORIGIN;
D O I
10.1016/j.canlet.2025.217793
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Three-dimensional patient-derived organoids (PDOs) have emerged as a powerful model for investigating the molecular and cellular mechanisms underlying bladder cancer, particularly in the context of cancer stem cells (CSCs) and drug screening. However, a significant limitation of conventional PDOs is the absence of tumor microenvironment (TME), which includes critical stromal, immune and microbial components that influence tumor behavior and treatment response. In this review, we provide a comprehensive overview of the recent advancements in PDO co-culture systems designed to integrate TME elements. Additionally, we emphasize the role of biomedical engineering technologies, such as 3D bioprinting and organoids-on-a-chip, in enhancing the physiological relevance of these models. Furthermore, we explore how bladder PDO co-culture systems are applied in research on bladder CSC characterization, evolution and treatment responses. Finally, we discuss future directions for improving PDO systems to achieve more accurate preclinical modeling and drug discovery.
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页数:10
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