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。

Q4 Biochemistry, Genetics and Molecular Biology
Mahsa Mollapour Sisakht, Shirin Hekmatirad
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引用次数: 0

摘要

类器官是由组织样本、诱导多能干细胞(iPSCs)和/或成体干细胞在体外生成的三维结构。患者源性类器官(PDOs)是生理上最相关的培养系统之一,它紧密地概括了原始组织的组织学和功能特征。它们可以在实验室中用于各种应用,包括再生医学、药物筛选、个性化医学和靶向治疗。自2009年以来,已报道了多个器官的类器官分离和培养方案,如结肠、胃、肝、肺、脑、乳腺和膀胱。在这里,我们描述了一种分离和培养来自膀胱切除术或经尿道膀胱肿瘤切除术(TUR)患者的膀胱肿瘤类器官的方案。除了传统的方法,我们介绍了一种成本效益高的替代方法,利用海藻酸钠水凝胶和成纤维细胞条件培养基(FCM)。该策略提供了一个可重复的、无xeno的、低成本的平台,非常适合临床研究和资源有限的实验室环境。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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来源期刊
Methods in molecular biology
Methods in molecular biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.00
自引率
0.00%
发文量
3536
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.
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