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损伤程序塑造胶质母细胞瘤。

Injury programs shape glioblastoma.

作者信息

Brooks Lucy J, Simpson Ragdale Holly, Hill Ciaran Scott, Clements Melanie, Parrinello Simona

机构信息

Samantha Dickson Brain Cancer Unit, Department of Cancer Biology, University College London Cancer Institute, London, UK.

Samantha Dickson Brain Cancer Unit, Department of Cancer Biology, University College London Cancer Institute, London, UK.

出版信息

Trends Neurosci. 2022 Nov;45(11):865-876. doi: 10.1016/j.tins.2022.08.006. Epub 2022 Sep 9.

DOI:10.1016/j.tins.2022.08.006
PMID:36089406
Abstract

Glioblastoma is the most common and aggressive primary brain cancer in adults and is almost universally fatal due to its stark therapeutic resistance. During the past decade, although survival has not substantially improved, major advances have been made in our understanding of the underlying biology. It has become clear that these devastating tumors recapitulate features of neurodevelopmental hierarchies which are influenced by the microenvironment. Emerging evidence also highlights a prominent role for injury responses in steering cellular phenotypes and contributing to tumor heterogeneity. This review highlights how the interplay between injury and neurodevelopmental programs impacts on tumor growth, invasion, and treatment resistance, and discusses potential therapeutic considerations in view of these findings.

摘要

胶质母细胞瘤是成人中最常见且侵袭性最强的原发性脑癌,由于其极强的治疗抗性,几乎无一例外都会导致死亡。在过去十年间,尽管生存率并未显著提高,但我们对其潜在生物学特性的理解取得了重大进展。已经明确的是,这些毁灭性肿瘤重现了受微环境影响的神经发育层级特征。新出现的证据还凸显了损伤反应在引导细胞表型和导致肿瘤异质性方面的重要作用。本综述强调了损伤与神经发育程序之间的相互作用如何影响肿瘤生长、侵袭和治疗抗性,并鉴于这些发现讨论了潜在的治疗考量。

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Injury programs shape glioblastoma.损伤程序塑造胶质母细胞瘤。
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Tumor microenvironment tenascin-C promotes glioblastoma invasion and negatively regulates tumor proliferation.肿瘤微环境中的腱生蛋白-C促进胶质母细胞瘤的侵袭,并对肿瘤增殖起负向调节作用。
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引用本文的文献

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Axonal injury is a targetable driver of glioblastoma progression.轴突损伤是胶质母细胞瘤进展的一个可靶向驱动因素。
Nature. 2025 Aug 20. doi: 10.1038/s41586-025-09411-2.
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Detecting glioblastoma infiltration beyond conventional imaging tumour margins using MTE-NODDI.使用MTE-NODDI检测胶质母细胞瘤超出传统影像肿瘤边界的浸润情况。
Imaging Neurosci (Camb). 2025 Feb 18;3. doi: 10.1162/imag_a_00472. eCollection 2025.
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Targeting the glioblastoma resection margin with locoregional nanotechnologies.利用局部纳米技术靶向胶质母细胞瘤切除边缘。
Nat Rev Clin Oncol. 2025 May 14. doi: 10.1038/s41571-025-01020-2.
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Multi-omics analysis identifies novels genes involved in glioma prognosis.多组学分析鉴定出与胶质瘤预后相关的新基因。
Sci Rep. 2025 Feb 17;15(1):5806. doi: 10.1038/s41598-025-90658-0.
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Single-cell multi-omics sequencing uncovers region-specific plasticity of glioblastoma for complementary therapeutic targeting.单细胞多组学测序揭示胶质母细胞瘤的区域特异性可塑性,用于互补的治疗靶点。
Sci Adv. 2024 Nov 22;10(47):eadn4306. doi: 10.1126/sciadv.adn4306.
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High expression of BTN3A1 is associated with clinical and immunological characteristics and predicts a poor prognosis in advanced human gliomas.BTN3A1 的高表达与临床和免疫学特征相关,并预测晚期人类神经胶质瘤预后不良。
Front Immunol. 2024 May 28;15:1397486. doi: 10.3389/fimmu.2024.1397486. eCollection 2024.
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Therapeutic Targeting of Glioblastoma and the Interactions with Its Microenvironment.胶质母细胞瘤的治疗靶点及其与微环境的相互作用
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Molecular landscapes of glioblastoma cell lines revealed a group of patients that do not benefit from tumor suppressor expression.胶质母细胞瘤细胞系的分子图谱揭示了一组无法从肿瘤抑制因子表达中获益的患者。
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