{"title":"患者来源的膀胱肿瘤类器官分离和培养:传统和降低成本的策略。","authors":"Mahsa Mollapour Sisakht, Shirin Hekmatirad","doi":"10.1007/7651_2025_664","DOIUrl":null,"url":null,"abstract":"<p><p>Organoids are three-dimensional structures generated in vitro from tissue samples, induced pluripotent stem cells (iPSCs), and/or adult stem cells. Patient-derived organoids (PDOs) represent one of the most physiologically relevant culture systems, closely recapitulating the histological and functional features of the original tissue. They can be established in the laboratory for various applications, including regenerative medicine, drug screening, personalized medicine, and targeted therapy. Since 2009, organoid isolation and culture protocols have been reported for multiple organs, such as the colon, stomach, liver, lung, brain, breast, and bladder. Here, we describe a protocol for the isolation and culture of bladder tumor organoids derived from patients undergoing cystectomy or transurethral resection of bladder tumor (TUR). In addition to the conventional methodology, we introduce a cost-effective alternative approach utilizing sodium alginate hydrogel and fibroblast-conditioned medium (FCM). This strategy offers a reproducible, xeno-free, and low-cost platform that is well suited for both clinical research and resource-limited laboratory settings.</p>","PeriodicalId":18490,"journal":{"name":"Methods in molecular biology","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Patient-Derived Bladder Tumor Organoids Isolation and Culture: Conventional and Cost-Reduction Strategy.\",\"authors\":\"Mahsa Mollapour Sisakht, Shirin Hekmatirad\",\"doi\":\"10.1007/7651_2025_664\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Organoids are three-dimensional structures generated in vitro from tissue samples, induced pluripotent stem cells (iPSCs), and/or adult stem cells. Patient-derived organoids (PDOs) represent one of the most physiologically relevant culture systems, closely recapitulating the histological and functional features of the original tissue. They can be established in the laboratory for various applications, including regenerative medicine, drug screening, personalized medicine, and targeted therapy. Since 2009, organoid isolation and culture protocols have been reported for multiple organs, such as the colon, stomach, liver, lung, brain, breast, and bladder. Here, we describe a protocol for the isolation and culture of bladder tumor organoids derived from patients undergoing cystectomy or transurethral resection of bladder tumor (TUR). In addition to the conventional methodology, we introduce a cost-effective alternative approach utilizing sodium alginate hydrogel and fibroblast-conditioned medium (FCM). This strategy offers a reproducible, xeno-free, and low-cost platform that is well suited for both clinical research and resource-limited laboratory settings.</p>\",\"PeriodicalId\":18490,\"journal\":{\"name\":\"Methods in molecular biology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-09-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Methods in molecular biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/7651_2025_664\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Biochemistry, Genetics and Molecular Biology\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Methods in molecular biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/7651_2025_664","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
Patient-Derived Bladder Tumor Organoids Isolation and Culture: Conventional and Cost-Reduction Strategy.
Organoids are three-dimensional structures generated in vitro from tissue samples, induced pluripotent stem cells (iPSCs), and/or adult stem cells. Patient-derived organoids (PDOs) represent one of the most physiologically relevant culture systems, closely recapitulating the histological and functional features of the original tissue. They can be established in the laboratory for various applications, including regenerative medicine, drug screening, personalized medicine, and targeted therapy. Since 2009, organoid isolation and culture protocols have been reported for multiple organs, such as the colon, stomach, liver, lung, brain, breast, and bladder. Here, we describe a protocol for the isolation and culture of bladder tumor organoids derived from patients undergoing cystectomy or transurethral resection of bladder tumor (TUR). In addition to the conventional methodology, we introduce a cost-effective alternative approach utilizing sodium alginate hydrogel and fibroblast-conditioned medium (FCM). This strategy offers a reproducible, xeno-free, and low-cost platform that is well suited for both clinical research and resource-limited laboratory settings.
期刊介绍:
For over 20 years, biological scientists have come to rely on the research protocols and methodologies in the critically acclaimed Methods in Molecular Biology series. The series was the first to introduce the step-by-step protocols approach that has become the standard in all biomedical protocol publishing. Each protocol is provided in readily-reproducible step-by-step fashion, opening with an introductory overview, a list of the materials and reagents needed to complete the experiment, and followed by a detailed procedure that is supported with a helpful notes section offering tips and tricks of the trade as well as troubleshooting advice.