Li Shengjie, Ren Jun, Wu Jianing, Xia Zuguang, Li Yingzhu, Li Chengxun, Cao Wenjun
Department of Clinical Laboratory, Eye & ENT Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Department of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.
Leukemia. 2025 May;39(5):1169-1183. doi: 10.1038/s41375-025-02562-1. Epub 2025 Mar 18.
Primary central nervous system lymphoma (PCNSL) exhibits substantial intratumoural and intertumoural heterogeneity, complicating the development of effective treatment methods. Existing in vitro models fail to simulate the cellular and mutational diversity of native tumours and require prolonged generation times. Therefore, we developed a culture method for patient-derived PCNSL organoids (CLOs) and evaluated the organoids through extensive molecular characterisation, histopathological analysis, single-nucleus RNA sequencing, bulk RNA sequencing and whole-exome sequencing. These CLOs accurately mimicked the histological attributes, gene expression landscapes and mutational profiles of their original tumours. Single-nucleus RNA sequencing also revealed that CLOs maintained cell-type heterogeneity and the molecular signatures of their original tumours. CLOs were generated within 2 weeks, demonstrating rapid development and reliability. Therapeutic profiling was performed on three selected CLOs treated with four standard drugs. The CLOs exhibited specific sensitivity to methotrexate, and resistance to dexamethasone, ibrutinib and rituximab, suggesting that CLOs may be valuable tools for reflecting drug sensitivities. Taken together, these results emphasise that CLOs effectively emulate the key characteristics of PCNSL, increasing the understanding of the genetic landscape of this complex disease. CLOs provide a rapid and reliable platform for exploring individualised treatment strategies, potentially accelerating the transition of research findings to clinical practice.
原发性中枢神经系统淋巴瘤(PCNSL)表现出显著的肿瘤内和肿瘤间异质性,这使得有效治疗方法的开发变得复杂。现有的体外模型无法模拟天然肿瘤的细胞和突变多样性,且生成时间较长。因此,我们开发了一种用于患者来源的PCNSL类器官(CLOs)的培养方法,并通过广泛的分子表征、组织病理学分析、单核RNA测序、批量RNA测序和全外显子组测序对类器官进行了评估。这些CLOs准确地模拟了其原始肿瘤的组织学特征、基因表达图谱和突变谱。单核RNA测序还显示,CLOs维持了细胞类型的异质性及其原始肿瘤的分子特征。CLOs在2周内生成,显示出快速发育和可靠性。对三种选定的用四种标准药物处理的CLOs进行了治疗分析。CLOs对甲氨蝶呤表现出特异性敏感性,对地塞米松、伊布替尼和利妥昔单抗具有抗性,这表明CLOs可能是反映药物敏感性的有价值工具。综上所述,这些结果强调CLOs有效地模拟了PCNSL的关键特征,增加了对这种复杂疾病基因图谱的理解。CLOs为探索个体化治疗策略提供了一个快速且可靠的平台,有可能加速研究结果向临床实践的转化。