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肿瘤微环境对于原发性神经胶质瘤中细胞状态的维持至关重要。

Tumor Microenvironment Is Critical for the Maintenance of Cellular States Found in Primary Glioblastomas.

机构信息

Caryl and Israel Englander Institute for Precision Medicine, Institute for Computational Biomedicine, Weill Cornell Medicine, New York, New York.

Tri-Institutional Program in Computational Biology and Medicine, New York, New York.

出版信息

Cancer Discov. 2020 Jul;10(7):964-979. doi: 10.1158/2159-8290.CD-20-0057. Epub 2020 Apr 6.

Abstract

Glioblastoma (GBM), an incurable tumor, remains difficult to model and more importantly to treat due to its genetic/epigenetic heterogeneity and plasticity across cellular states. The ability of current tumor models to recapitulate the cellular states found in primary tumors remains unexplored. To address this issue, we compared single-cell RNA sequencing of tumor cells from 5 patients across four patient-specific glioblastoma stem cell (GSC)-derived model types, including glioma spheres, tumor organoids, glioblastoma cerebral organoids (GLICO), and patient-derived xenografts. We find that GSCs within the GLICO model are enriched for a neural progenitor-like cell subpopulation and recapitulate the cellular states and their plasticity found in the corresponding primary parental tumors. These data demonstrate how the contribution of a neuroanatomically accurate human microenvironment is critical and sufficient for recapitulating the cellular states found in human primary GBMs, a principle that may likely apply to other tumor models. SIGNIFICANCE: It has been unclear how well different patient-derived GBM models are able to recreate the full heterogeneity of primary tumors. Here, we provide a complete transcriptomic characterization of the major model types. We show that the microenvironment is crucial for recapitulating GSC cellular states, highlighting the importance of tumor-host cell interactions...

摘要

胶质母细胞瘤(GBM)是一种无法治愈的肿瘤,由于其遗传/表观遗传异质性和跨细胞状态的可塑性,仍然难以建模,更难以治疗。目前的肿瘤模型是否能够再现原发性肿瘤中存在的细胞状态仍未得到探索。为了解决这个问题,我们比较了来自 5 名患者的肿瘤细胞的单细胞 RNA 测序,这些患者跨越了 4 种患者特异性胶质母细胞瘤干细胞(GSC)衍生的模型类型,包括神经胶质瘤球体、肿瘤类器官、胶质母细胞瘤大脑类器官(GLICO)和患者来源的异种移植物。我们发现,GLICO 模型中的 GSCs 富含类似于神经祖细胞的细胞亚群,并再现了相应原发性亲本肿瘤中发现的细胞状态及其可塑性。这些数据表明,神经解剖学上准确的人类微环境的贡献对于再现人类原发性 GBM 中发现的细胞状态是多么重要和充分,这一原则可能适用于其他肿瘤模型。意义:不同的患者来源的 GBM 模型能够在多大程度上重现原发性肿瘤的全部异质性一直不清楚。在这里,我们提供了主要模型类型的完整转录组特征描述。我们表明,微环境对于再现 GSC 细胞状态至关重要,突出了肿瘤-宿主细胞相互作用的重要性...

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