Department of Medicine, Division of Medical Oncology, Duke University Medical Center, Durham, North Carolina.
Center for Genomics and Computational Biology, Duke University, Durham, North Carolina.
Cancer Res Commun. 2023 Sep 27;3(9):1952-1958. doi: 10.1158/2767-9764.CRC-23-0109.
Patient-derived organoids are a useful platform for identification and testing of novel precision oncology approaches. Patient-derived organoids are generated by direct culture of patient samples. However, prior to development into patient-derived organoids, these samples are often processed for clinical use, opening the potential for contamination by Mycoplasma and other microbes. While most microbes can be detected by visual inspection, Mycoplasma can go undetected and have substantial impacts on assay results. Given the increased use of patient-derived organoids, there is a growing need for a standardized protocol to detect and remove Mycoplasma from organoid models. In the current study, we report a procedure for Mycoplasma removal by passaging organoids through mice as patient-derived organoid xenografts. In vivo passage of patient-derived organoids followed by re-establishment was 100% effective at decontaminating colorectal patient-derived organoids (n = 9), based on testing with the Sigma LookOut Mycoplasma PCR Detection Kit. This process can serve as a method to re-establish contaminated patient-derived organoids, which represent precious models to study patient-specific genomic features and treatment responses.
Organoids are valuable models of cancer. Mycoplasma contamination can alter organoid drug sensitivity, so there is a need for a standardized protocol to detect and remove Mycoplasma from organoids. We report a simple procedure for removing Mycoplasma from organoids via in vivo passaging through mice followed by re-establishment of organoids.
患者来源的类器官是鉴定和测试新型精准肿瘤学方法的有用平台。患者来源的类器官是通过直接培养患者样本生成的。然而,在这些样本发展为患者来源的类器官之前,它们通常经过处理以供临床使用,从而有被支原体和其他微生物污染的潜在风险。虽然大多数微生物可以通过肉眼观察检测到,但支原体可能无法被检测到,并且会对检测结果产生重大影响。鉴于患者来源的类器官使用的增加,越来越需要一种标准化的方案来检测和去除类器官模型中的支原体。在当前的研究中,我们报告了一种通过将类器官作为患者来源的类器官异种移植物传代到小鼠体内来去除支原体的程序。基于 Sigma LookOut 支原体 PCR 检测试剂盒的检测,9 例结直肠患者来源的类器官(n=9)的体内传代后再建立的方法 100%有效去除污染。该过程可作为重新建立污染的患者来源类器官的方法,这些类器官是研究患者特异性基因组特征和治疗反应的宝贵模型。
类器官是癌症的有价值模型。支原体污染会改变类器官的药物敏感性,因此需要一种标准化的方案来检测和去除类器官中的支原体。我们报告了一种通过体内传代小鼠并重新建立类器官来从类器官中去除支原体的简单程序。