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非 WNT/非 SHH 髓母细胞瘤的临床不利转录组亚型与增殖和祖细胞样细胞亚群占优势有关。

Clinically unfavorable transcriptome subtypes of non-WNT/non-SHH medulloblastomas are associated with a predominance in proliferating and progenitor-like cell subpopulations.

机构信息

Hopp Children's Cancer Center Heidelberg (KiTZ), Heidelberg, Germany.

Division of Pediatric Neuro-Oncology, German Cancer Research Center (DKFZ), German Cancer Consortium (DKTK), Heidelberg, Germany.

出版信息

Acta Neuropathol. 2024 Jun 7;147(1):95. doi: 10.1007/s00401-024-02746-6.

DOI:10.1007/s00401-024-02746-6
PMID:38847845
Abstract

The non-WNT/non-SHH (Grp3/Grp4) medulloblastomas (MBs) include eight second-generation subgroups (SGS; I-VIII) each with distinct molecular and clinical characteristics. Recently, we also identified two prognostically relevant transcriptome subtypes within each SGS MB, which are associated with unique gene expression signatures and signaling pathways. These prognostic subsets may be in connection to the intra-tumoral cell landscape that underlies SGS MB clinical-molecular diversity. Here, we performed a deconvolution analysis of the Grp3/Grp4 MB bulk RNA profiles using the previously identified single-cell RNA-seq reference dataset and focusing on variability in the cellular composition of SGS MB. RNA deconvolution analysis of the Grp3/Grp4 MB disclosed the subgroup-specific neoplastic cell subpopulations. Neuronally differentiated axodendritic GP3-C1 and glutamatergic GP4-C1 subpopulations were distributed within Grp3- and Grp4-associated SGS MB, respectively. Progenitor GP3-B2 subpopulation was prominent in aggressive SGS II MB, whereas photoreceptor/visual perception GP3/4-C2 cell content was typical for SGS III/IV MB. The current study also revealed significant variability in the proportions of cell subpopulations between clinically relevant SGS MB transcriptome subtypes, where unfavorable cohorts were enriched with cell cycle and progenitor-like cell subpopulations and, vice versa, favorable subtypes were composed of neuronally differentiated cell fractions predominantly. A higher than median proportion of proliferating and progenitor cell subpopulations conferred the shortest survival of the Grp3 and Grp 4 MB, and similar survival associations were identified for all SGS MB except SGS IV MB. In summary, the recently identified clinically relevant Grp3/Grp4 MB transcriptome subtypes are composed of different cell populations. Future studies should aim to validate the prognostic and therapeutic role of the identified Grp3/Grp4 MB inter-tumoral cellular heterogeneity. The application of the single-cell techniques on each SGS MB separately could help to clarify the clinical significance of subgroup-specific variability in tumor cell content and its relation with prognostic transcriptome signatures identified before.

摘要

非 WNT/非 SHH(Grp3/Grp4)髓母细胞瘤(MB)包括 8 个第二代亚组(SGS;I-VIII),每个亚组都具有不同的分子和临床特征。最近,我们还在每个 SGS MB 内确定了两个具有预后相关性的转录组亚型,它们与独特的基因表达特征和信号通路相关。这些预后亚组可能与 SGS MB 临床-分子多样性所基于的肿瘤内细胞景观有关。在这里,我们使用之前确定的单细胞 RNA-seq 参考数据集对 Grp3/Grp4 MB 批量 RNA 谱进行了去卷积分析,重点关注 SGS MB 中细胞组成的可变性。Grp3/Grp4 MB 的 RNA 去卷积分析揭示了亚组特异性的肿瘤细胞亚群。神经分化的轴突树突 GP3-C1 和谷氨酸能 GP4-C1 亚群分别分布在 Grp3 和 Grp4 相关的 SGS MB 中。侵袭性 SGS II MB 中突出的是祖细胞 GP3-B2 亚群,而 SGS III/IV MB 中典型的是感光器/视觉感知 GP3/4-C2 细胞含量。本研究还揭示了临床上相关的 SGS MB 转录组亚型之间细胞亚群比例的显著差异,其中不利队列富含细胞周期和祖细胞样细胞亚群,反之,有利亚型主要由神经元分化的细胞分数组成。增殖和祖细胞亚群的比例高于中位数,使 Grp3 和 Grp 4 MB 的生存时间最短,除 SGS IV MB 外,所有 SGS MB 都存在类似的生存关联。总之,最近确定的具有临床意义的 Grp3/Grp4 MB 转录组亚型由不同的细胞群组成。未来的研究应旨在验证所确定的 Grp3/Grp4 MB 肿瘤间细胞异质性的预后和治疗作用。对每个 SGS MB 分别应用单细胞技术可以帮助阐明肿瘤细胞含量的亚组特异性变异性的临床意义及其与之前确定的预后转录组特征的关系。

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本文引用的文献

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Mapping pediatric brain tumors to their origins in the developing cerebellum.将小儿脑瘤定位到发育中的小脑。
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Transcriptome analysis stratifies second-generation non-WNT/non-SHH medulloblastoma subgroups into clinically tractable subtypes.转录组分析将第二代非 WNT/非 SHH 髓母细胞瘤亚组细分为具有临床可操作性的亚型。
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