髓母细胞瘤未标记通路亚型肿瘤间异质性的多组学分析。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY
Brain Tumor Pathology Pub Date : 2021-07-01 Epub Date: 2021-06-28 DOI:10.1007/s10014-021-00400-7
Zhicen Li, Yifan Wei, Yanqiu Shao, Lei Tang, Jian Gong
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引用次数: 2

摘要

髓母细胞瘤是一种常见的儿童恶性脑肿瘤。共有4个一致的分子亚群(WNT、SHH、Group3和Group4)。第3组和第4组肿瘤表现出很大程度的转录重叠,并且都不是来自确切的通路畸变。我们通过多组学单细胞分析研究了髓母细胞瘤的转录和染色质可及性。我们的工作确定了第3组、第4组和第3/4组中间亚组的肿瘤间和肿瘤内异质性。每个肿瘤的无监督簇鉴定出9个具有转录谱的细胞簇和6个具有染色质可及性谱的细胞簇。在基于开放染色质单细胞谱的特殊簇中,OTX2具有最高的活性和表达水平。我们在OTX2靶基因中发现了多个重要的靶基因,这对预后有意义。我们从转录和染色质可及性谱分析了呈现预期亚群分布的拷贝数变化。总的来说,这些数据为第3组和第4组髓母细胞瘤提供了新的见解,并提供了潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-omics analysis of intertumoral heterogeneity within medulloblastoma uncharted-pathway subtypes.

Medulloblastoma is a common pediatric malignant brain tumor. There were four consensus molecular subgroups (WNT, SHH, Group3 and Group4). Group 3 and Group 4 tumors exhibited a great degree of transcriptional overlap, and were neither derived from exact pathway aberration. We investigated transcriptional and chromatin accessibility of medulloblastoma by multi-omics single-cell analysis. Our work identified inter- and intra-tumoral heterogeneity within the Group 3, Group 4 and Group 3/4 intermediate subgroups. Unsupervised cluster of each tumor identified 9 cell clusters with transcriptional profiles and 6 cell clusters with chromatin accessibility profiles. OTX2 had the highest activity and expression level across the clusters in a special cluster based on open chromatin single-cell profilings. We identified multiple genes as a significant targeted gene within the OTX2 target genes, which made sense in prognosis. We analyzed the copy-number-variations which presented with expected subgroup distribution from transcriptional and chromatin accessibility profiles. Collectively, these data provide novel insights into Group 3 and Group 4 medulloblastoma and provide a potential therapeutic target.

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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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