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儿童脑胶质瘤和弥漫性内在脑桥胶质瘤细胞亚克隆群体之间的功能多样性和协同作用。

Functional diversity and cooperativity between subclonal populations of pediatric glioblastoma and diffuse intrinsic pontine glioma cells.

机构信息

Centre for Evolution and Cancer, The Institute of Cancer Research, London, UK.

Division of Molecular Pathology, The Institute of Cancer Research, London, UK.

出版信息

Nat Med. 2018 Aug;24(8):1204-1215. doi: 10.1038/s41591-018-0086-7. Epub 2018 Jul 2.

Abstract

The failure to develop effective therapies for pediatric glioblastoma (pGBM) and diffuse intrinsic pontine glioma (DIPG) is in part due to their intrinsic heterogeneity. We aimed to quantitatively assess the extent to which this was present in these tumors through subclonal genomic analyses and to determine whether distinct tumor subpopulations may interact to promote tumorigenesis by generating subclonal patient-derived models in vitro and in vivo. Analysis of 142 sequenced tumors revealed multiple tumor subclones, spatially and temporally coexisting in a stable manner as observed by multiple sampling strategies. We isolated genotypically and phenotypically distinct subpopulations that we propose cooperate to enhance tumorigenicity and resistance to therapy. Inactivating mutations in the H4K20 histone methyltransferase KMT5B (SUV420H1), present in <1% of cells, abrogate DNA repair and confer increased invasion and migration on neighboring cells, in vitro and in vivo, through chemokine signaling and modulation of integrins. These data indicate that even rare tumor subpopulations may exert profound effects on tumorigenesis as a whole and may represent a new avenue for therapeutic development. Unraveling the mechanisms of subclonal diversity and communication in pGBM and DIPG will be an important step toward overcoming barriers to effective treatments.

摘要

儿童脑胶质瘤(pGBM)和弥漫性内在脑桥胶质瘤(DIPG)未能开发出有效的治疗方法,部分原因是它们具有内在的异质性。我们旨在通过亚克隆基因组分析定量评估这些肿瘤中存在的这种情况的程度,并通过体外和体内生成亚克隆患者衍生模型来确定不同的肿瘤亚群是否可能通过相互作用来促进肿瘤发生。对 142 个测序肿瘤的分析表明,多种肿瘤亚克隆以稳定的方式共存于空间和时间上,这是通过多种采样策略观察到的。我们分离出了在体外和体内具有遗传和表型不同的亚群,我们提出这些亚群合作以增强肿瘤发生能力和对治疗的抵抗力。存在于<1%细胞中的 H4K20 组蛋白甲基转移酶 KMT5B(SUV420H1)的失活突变,通过趋化因子信号转导和整合素的调节,在体外和体内消除 DNA 修复并赋予相邻细胞更高的侵袭和迁移能力。这些数据表明,即使是罕见的肿瘤亚群也可能对整个肿瘤发生产生深远的影响,并且可能代表治疗开发的新途径。揭示 pGBM 和 DIPG 中亚克隆多样性和通讯的机制将是克服有效治疗障碍的重要一步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/760d/6086334/a87a9c725131/emss-77609-f001.jpg

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