• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

神经母细胞瘤细胞谱系表型和模型概述。

An overview of neuroblastoma cell lineage phenotypes and models.

机构信息

Graduate Program in Health Sciences, Pontifícia Universidade Católica do Paraná, Curitiba 80215-901, Brazil.

Instituto de Pesquisa Pelé Pequeno Príncipe, Faculdades Pequeno Príncipe, Curitiba 80250-060, Brazil.

出版信息

Exp Biol Med (Maywood). 2020 Dec;245(18):1637-1647. doi: 10.1177/1535370220949237. Epub 2020 Aug 12.

DOI:10.1177/1535370220949237
PMID:32787463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7802384/
Abstract

This review was conducted to present the main neuroblastoma (NB) clinical characteristics and the most common genetic alterations present in these pediatric tumors, highlighting their impact in tumor cell aggressiveness behavior, including metastatic development and treatment resistance, and patients' prognosis. The distinct three NB cell lineage phenotypes, S-type, N-type, and I-type, which are characterized by unique cell surface markers and gene expression patterns, are also reviewed. Finally, an overview of the most used NB cell lines currently available for studies and their unique cellular and molecular characteristics, which should be taken into account for the selection of the most appropriate model for NB pre-clinical studies, is presented. These valuable models can be complemented by the generation of NB reprogrammed tumor cells or organoids, derived directly from patients' tumor specimens, in the direction toward personalized medicine.

摘要

这篇综述旨在介绍神经母细胞瘤(NB)的主要临床特征和这些儿科肿瘤中常见的遗传改变,强调它们对肿瘤细胞侵袭性行为的影响,包括转移的发展和治疗耐药性以及患者的预后。还回顾了具有独特细胞表面标志物和基因表达模式的三种不同的 NB 细胞谱系表型,S 型、N 型和 I 型。最后,概述了目前用于研究的最常用的 NB 细胞系及其独特的细胞和分子特征,在选择最适合 NB 临床前研究的模型时应考虑这些特征。这些有价值的模型可以通过直接从患者肿瘤标本中衍生的 NB 重编程肿瘤细胞或类器官来补充,朝着个性化医疗的方向发展。

相似文献

1
An overview of neuroblastoma cell lineage phenotypes and models.神经母细胞瘤细胞谱系表型和模型概述。
Exp Biol Med (Maywood). 2020 Dec;245(18):1637-1647. doi: 10.1177/1535370220949237. Epub 2020 Aug 12.
2
Considerations for the Use of SH-SY5Y Neuroblastoma Cells in Neurobiology.神经生物学中使用 SH-SY5Y 神经母细胞瘤细胞的注意事项。
Methods Mol Biol. 2021;2311:9-23. doi: 10.1007/978-1-0716-1437-2_2.
3
MicroRNA-149 is associated with clinical outcome in human neuroblastoma and modulates cancer cell proliferation through Rap1 independent of MYCN amplification.微小RNA-149与人类神经母细胞瘤的临床预后相关,并通过不依赖MYCN扩增的Rap1调节癌细胞增殖。
Biochimie. 2017 Aug;139:1-8. doi: 10.1016/j.biochi.2017.04.011. Epub 2017 Apr 27.
4
Functional sphere profiling reveals the complexity of neuroblastoma tumor-initiating cell model.功能球谱分析揭示了神经母细胞瘤肿瘤起始细胞模型的复杂性。
Neoplasia. 2011 Oct;13(10):991-1004. doi: 10.1593/neo.11800.
5
Transient treatment with epigenetic modifiers yields stable neuroblastoma stem cells resembling aggressive large-cell neuroblastomas.短暂处理表观遗传修饰剂可产生类似于侵袭性大细胞神经母细胞瘤的稳定神经母细胞瘤干细胞。
Proc Natl Acad Sci U S A. 2013 Apr 9;110(15):6097-102. doi: 10.1073/pnas.1118262110. Epub 2013 Mar 11.
6
Identification of neuroblastoma cell lines with uncommon TAZ/mesenchymal stromal cell phenotype with strong suppressive activity on natural killer cells.鉴定具有罕见 TAZ/间充质基质细胞表型的神经母细胞瘤细胞系,其对自然杀伤细胞具有强烈的抑制活性。
J Immunother Cancer. 2021 Jan;9(1). doi: 10.1136/jitc-2020-001313.
7
Patient-derived organoids (PDOs) as a novel in vitro model for neuroblastoma tumours.患者来源的类器官(PDO)作为神经母细胞瘤肿瘤的新型体外模型。
BMC Cancer. 2019 Oct 21;19(1):970. doi: 10.1186/s12885-019-6149-4.
8
Sendai virus-mediated expression of reprogramming factors promotes plasticity of human neuroblastoma cells.仙台病毒介导的重编程因子表达促进人神经母细胞瘤细胞的可塑性。
Cancer Sci. 2015 Oct;106(10):1351-61. doi: 10.1111/cas.12746. Epub 2015 Aug 18.
9
FOXD3 is a novel tumor suppressor that affects growth, invasion, metastasis and angiogenesis of neuroblastoma.FOXD3是一种新型肿瘤抑制因子,可影响神经母细胞瘤的生长、侵袭、转移和血管生成。
Oncotarget. 2013 Nov;4(11):2021-44. doi: 10.18632/oncotarget.1579.
10
Generation and characterization of novel local and metastatic human neuroblastoma variants.新型局部和转移性人类神经母细胞瘤变体的生成与特性分析
Neoplasia. 2008 Aug;10(8):816-27. doi: 10.1593/neo.08402.

引用本文的文献

1
Amniotic membrane promotes doxorubicin potency by suppressing SH-SY5Y neuroblastoma cell angiogenesis.羊膜通过抑制SH-SY5Y神经母细胞瘤细胞血管生成来增强阿霉素的效力。
BMC Cancer. 2025 Jun 19;25(1):1021. doi: 10.1186/s12885-025-14442-z.
2
Interplay Between the Epigenome, the Microenvironment, and the Immune System in Neuroblastoma.神经母细胞瘤中表观基因组、微环境与免疫系统之间的相互作用
Cancers (Basel). 2025 May 29;17(11):1812. doi: 10.3390/cancers17111812.
3
α-Enolase and γ-Enolase Expression in Enriched S- and N-Type SH-SY5Y Cells: Regulatory Role of Cathepsin X.α-烯醇化酶和γ-烯醇化酶在富集的S型和N型SH-SY5Y细胞中的表达:组织蛋白酶X的调节作用
Mol Neurobiol. 2025 Apr 3. doi: 10.1007/s12035-025-04898-2.
4
Exploring high-throughput drug sensitivity testing in neuroblastoma cell lines and patient-derived tumor organoids in the era of precision medicine.在精准医学时代探索神经母细胞瘤细胞系和患者来源的肿瘤类器官中的高通量药物敏感性测试。
Eur J Cancer. 2025 Mar 11;218:115275. doi: 10.1016/j.ejca.2025.115275. Epub 2025 Feb 8.
5
A Novel and Robust Protocol for Differentiation of SH-SY5Y Neuroblastoma Cells into Neuron Like Cells.一种将SH-SY5Y神经母细胞瘤细胞分化为神经元样细胞的新颖且稳健的方案。
Noro Psikiyatr Ars. 2024 Aug 19;67(3):208-212. doi: 10.29399/npa.28510. eCollection 2024.
6
Developing targeted therapies for neuroblastoma by dissecting the effects of metabolic reprogramming on tumor microenvironments and progression.通过剖析代谢重编程对肿瘤微环境和进展的影响,为神经母细胞瘤开发靶向治疗方法。
Theranostics. 2024 May 27;14(9):3439-3469. doi: 10.7150/thno.93962. eCollection 2024.
7
Lysophosphatidic Acid Stimulates Mitogenic Activity and Signaling in Human Neuroblastoma Cells through a Crosstalk with Anaplastic Lymphoma Kinase.溶血磷脂酸通过与间变性淋巴瘤激酶的串扰刺激人神经母细胞瘤细胞的有丝分裂活性和信号转导。
Biomolecules. 2024 May 28;14(6):631. doi: 10.3390/biom14060631.
8
Integrated re-analysis of transcriptomic and proteomic datasets reveals potential mechanisms for Zika viral-based oncolytic therapy in neuroblastoma.整合转录组和蛋白质组数据集的重新分析揭示了寨卡病毒在神经母细胞瘤溶瘤治疗中的潜在机制。
F1000Res. 2024 May 21;12:719. doi: 10.12688/f1000research.132627.3. eCollection 2023.
9
Identification of GB3 as a Novel Biomarker of Tumor-Derived Vasculature in Neuroblastoma Using a Stiffness-Based Model.使用基于硬度的模型鉴定GB3作为神经母细胞瘤中肿瘤衍生血管的新型生物标志物。
Cancers (Basel). 2024 Mar 5;16(5):1060. doi: 10.3390/cancers16051060.
10
A Potential Prognostic Gene Signature Associated with p53-Dependent NTRK1 Activation and Increased Survival of Neuroblastoma Patients.一种与p53依赖性NTRK1激活及神经母细胞瘤患者生存率提高相关的潜在预后基因特征。
Cancers (Basel). 2024 Feb 8;16(4):722. doi: 10.3390/cancers16040722.

本文引用的文献

1
Applications of patient-derived tumor xenograft models and tumor organoids.患者来源肿瘤异种移植模型和肿瘤类器官的应用。
J Hematol Oncol. 2020 Jan 7;13(1):4. doi: 10.1186/s13045-019-0829-z.
2
Emerging organoid models: leaping forward in cancer research.新兴类器官模型:癌症研究的飞跃。
J Hematol Oncol. 2019 Dec 29;12(1):142. doi: 10.1186/s13045-019-0832-4.
3
Patient-derived organoids (PDOs) as a novel in vitro model for neuroblastoma tumours.患者来源的类器官(PDO)作为神经母细胞瘤肿瘤的新型体外模型。
BMC Cancer. 2019 Oct 21;19(1):970. doi: 10.1186/s12885-019-6149-4.
4
Dual-Targeting AKT2 and ERK in cancer stem-like cells in neuroblastoma.双靶点作用于神经母细胞瘤中癌干细胞样细胞的AKT2和ERK
Oncotarget. 2019 Sep 24;10(54):5645-5659. doi: 10.18632/oncotarget.27210.
5
Clinical Features of Neuroblastoma With 11q Deletion: An Increase in Relapse Probabilities In Localized And 4S Stages.11q 缺失型神经母细胞瘤的临床特征:局部和 4S 期复发概率增加。
Sci Rep. 2019 Sep 24;9(1):13806. doi: 10.1038/s41598-019-50327-5.
6
Fibronectin in malignancy: Cancer-specific alterations, protumoral effects, and therapeutic implications.纤维连接蛋白在恶性肿瘤中的作用:肿瘤特异性改变、促肿瘤效应及治疗意义。
Semin Oncol. 2019 Jun;46(3):284-290. doi: 10.1053/j.seminoncol.2019.08.002. Epub 2019 Aug 27.
7
Upregulation of MAPK10, TUBB2B and RASL11B may contribute to the development of neuroblastoma.MAPK10、TUBB2B 和 RASL11B 的上调可能有助于神经母细胞瘤的发展。
Mol Med Rep. 2019 Oct;20(4):3475-3486. doi: 10.3892/mmr.2019.10589. Epub 2019 Aug 20.
8
Murine neuroblastoma cell lines developed by conditional reprogramming preserve heterogeneous phenotypes observed in vivo.通过条件重编程开发的鼠神经母细胞瘤细胞系保留了体内观察到的异质表型。
Lab Invest. 2020 Jan;100(1):38-51. doi: 10.1038/s41374-019-0297-7. Epub 2019 Aug 13.
9
A NOTCH feed-forward loop drives reprogramming from adrenergic to mesenchymal state in neuroblastoma.NOTCH 正向反馈环驱动神经母细胞瘤从肾上腺素能状态向间充质状态重编程。
Nat Commun. 2019 Apr 4;10(1):1530. doi: 10.1038/s41467-019-09470-w.
10
CADM1 is a TWIST1-regulated suppressor of invasion and survival.CADM1 是 TWIST1 调节的侵袭和存活抑制因子。
Cell Death Dis. 2019 Mar 25;10(4):281. doi: 10.1038/s41419-019-1515-3.