Inferred developmental origins of brain tumors from single-cell RNA-sequencing data.

IF 3.7 Q1 CLINICAL NEUROLOGY
Neuro-oncology advances Pub Date : 2025-01-23 eCollection Date: 2025-01-01 DOI:10.1093/noajnl/vdaf016
Su Wang, Rachel Naomi Curry, Malcolm F McDonald, Hyun Yong Koh, Anders W Erickson, Claudia L Kleinman, Michael D Taylor, Ganesh Rao, Benjamin Deneen, Arif O Harmanci, Akdes Serin Harmanci
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引用次数: 0

Abstract

Background: The reactivation of neurodevelopmental programs in cancer highlights parallel biological processes that occur in both normal development and brain tumors. Achieving a deeper understanding of how dysregulated developmental factors play a role in the progression of brain tumors is therefore crucial for identifying potential targets for therapeutic interventions. Single-cell RNA-sequencing (scRNA-Seq) provides an opportunity to understand how developmental programs are dysregulated and reinitiated in brain tumors at single-cell resolution. The aim of this study is to identify the developmental origins of brain tumors using scRNA-Seq data.

Methods: Here, we introduce COORS (Cell Of ORigin like CellS), a computational tool trained on developmental human brain single-cell datasets that annotates "developmental-like" cell states in brain tumors. COORS leverages cell type-specific multilayer perceptron models and incorporates a developmental cell type tree that reflects hierarchical relationships and models cell type probabilities.

Results: Applying COORS to various brain cancer datasets, including medulloblastoma (MB), glioma, and diffuse midline glioma (DMG), we identified developmental-like cells that represent putative cells of origin in these tumors. Our method provides both cell of origin classification and cell age regression, offering insights into the developmental cell types of tumor subgroups. COORS identified outer radial glia developmental cells within IDHWT glioma cells whereas oligodendrocyte precursor cells (OPCs) and neuronal-like cells in IDHMut. Interestingly, IDHMut subgroup cells that map to OPC show bimodal distributions that are both early and late weeks in development. Furthermore, COORS offers a valuable resource by providing novel markers linked to developmental states within MB, glioma, and DMG tumor subgroups.

Conclusions: Our work adds to our cumulative understanding of brain tumor heterogeneity and helps pave the way for tailored treatment strategies.

从单细胞rna测序数据推断脑肿瘤的发育起源。
背景:肿瘤中神经发育程序的再激活突出了正常发育和脑肿瘤中发生的平行生物学过程。因此,更深入地了解失调的发育因素如何在脑肿瘤的进展中发挥作用,对于确定治疗干预的潜在靶点至关重要。单细胞rna测序(scRNA-Seq)提供了一个在单细胞分辨率下了解脑肿瘤中发育程序是如何失调和重新启动的机会。本研究的目的是利用scRNA-Seq数据确定脑肿瘤的发育起源。方法:在这里,我们介绍了COORS (Cell Of ORigin like CellS),这是一种基于发育的人脑单细胞数据集训练的计算工具,用于注释脑肿瘤中的“发育样”细胞状态。COORS利用细胞类型特定的多层感知器模型,并结合了一个反映分层关系的发育细胞类型树,并对细胞类型概率进行建模。结果:将COORS应用于各种脑癌数据集,包括髓母细胞瘤(MB)、胶质瘤和弥漫性中线胶质瘤(DMG),我们确定了代表这些肿瘤中假定起源细胞的发育样细胞。我们的方法提供了细胞起源分类和细胞年龄回归,为肿瘤亚群的发育细胞类型提供了见解。COORS在IDHWT胶质瘤细胞中鉴定出外放射状胶质发育细胞,而在IDHMut胶质瘤细胞中鉴定出少突胶质前体细胞(OPCs)和神经元样细胞。有趣的是,映射到OPC的IDHMut亚群细胞在发育的早期和晚期都表现出双峰分布。此外,COORS通过提供与MB、胶质瘤和DMG肿瘤亚组的发育状态相关的新标记物,提供了有价值的资源。结论:我们的工作增加了我们对脑肿瘤异质性的累积理解,并有助于为量身定制的治疗策略铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
0.00%
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审稿时长
12 weeks
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