• 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

相似文献

1
Transcriptional profiling in an MPNST-derived cell line and normal human Schwann cells.对一种源自恶性周围神经鞘膜瘤的细胞系和正常人雪旺细胞进行转录谱分析。
Neuron Glia Biol. 2004 May;1(2):135-47. doi: 10.1017/s1740925x04000274.
2
Schwann cell lines derived from malignant peripheral nerve sheath tumors respond abnormally to platelet-derived growth factor-BB.源自恶性外周神经鞘瘤的施万细胞系对血小板衍生生长因子-BB反应异常。
J Neurosci Res. 2005 Feb 1;79(3):318-28. doi: 10.1002/jnr.20334.
3
Prostaglandin E(2) metabolism is activated in Schwann cell lines derived from human NF1 malignant peripheral nerve sheath tumors.源自人类1型神经纤维瘤病恶性外周神经鞘瘤的雪旺氏细胞系中,前列腺素E(2)代谢被激活。
Neuron Glia Biol. 2004 May;1(2):149-55. doi: 10.1017/S1740925X04000262.
4
Large-scale molecular comparison of human schwann cells to malignant peripheral nerve sheath tumor cell lines and tissues.人雪旺细胞与恶性外周神经鞘膜瘤细胞系及组织的大规模分子比较。
Cancer Res. 2006 Mar 1;66(5):2584-91. doi: 10.1158/0008-5472.CAN-05-3330.
5
Immune system evasion by peripheral nerve sheath tumor.周围神经鞘瘤对免疫系统的逃避
Neurosci Lett. 2006;397(1-2):126-9. doi: 10.1016/j.neulet.2005.12.027. Epub 2006 Jan 6.
6
NF1 deficiency causes Bcl-xL upregulation in Schwann cells derived from neurofibromatosis type 1-associated malignant peripheral nerve sheath tumors.NF1 缺失导致来源于神经纤维瘤病 1 相关恶性外周神经鞘瘤的雪旺细胞中 Bcl-xL 的上调。
Int J Oncol. 2013 Feb;42(2):657-66. doi: 10.3892/ijo.2012.1751. Epub 2012 Dec 24.
7
The Cellular Retinoic Acid Binding Protein 2 Promotes Survival of Malignant Peripheral Nerve Sheath Tumor Cells.细胞视黄酸结合蛋白2促进恶性外周神经鞘瘤细胞的存活。
Am J Pathol. 2017 Jul;187(7):1623-1632. doi: 10.1016/j.ajpath.2017.02.021. Epub 2017 May 11.
8
MEK inhibitors enhance therapeutic response towards ATRA in NF1 associated malignant peripheral nerve sheath tumors (MPNST) in-vitro.MEK抑制剂在体外增强了神经纤维瘤病1型相关恶性外周神经鞘瘤(MPNST)对全反式维甲酸的治疗反应。
PLoS One. 2017 Nov 13;12(11):e0187700. doi: 10.1371/journal.pone.0187700. eCollection 2017.
9
Transposon Mutagenesis-Guided CRISPR/Cas9 Screening Strongly Implicates Dysregulation of Hippo/YAP Signaling in Malignant Peripheral Nerve Sheath Tumor Development.转座子诱变引导的CRISPR/Cas9筛选强烈提示Hippo/YAP信号通路失调在恶性外周神经鞘瘤发生发展中起重要作用。
Cancers (Basel). 2021 Mar 30;13(7):1584. doi: 10.3390/cancers13071584.
10
R-Ras subfamily proteins elicit distinct physiologic effects and phosphoproteome alterations in neurofibromin-null MPNST cells.R-Ras 亚家族蛋白在神经纤维瘤病缺失型 MPNST 细胞中引起不同的生理效应和磷酸化蛋白质组改变。
Cell Commun Signal. 2021 Sep 16;19(1):95. doi: 10.1186/s12964-021-00773-4.

引用本文的文献

1
STING activation reprograms the microenvironment to sensitize NF1-related malignant peripheral nerve sheath tumors for immunotherapy.STING 激活重编程微环境使 NF1 相关恶性外周神经鞘瘤对免疫治疗敏感。
J Clin Invest. 2024 Mar 19;134(10):e176748. doi: 10.1172/JCI176748.
2
The +/- Immune Microenvironment: Dueling Roles in Neurofibroma Development and Malignant Transformation.±免疫微环境:在神经纤维瘤发生发展及恶性转化中的双重作用
Cancers (Basel). 2024 Feb 29;16(5):994. doi: 10.3390/cancers16050994.
3
Human Schwann Cells in vitro II. Passaging, Purification, Banking, and Labeling of Established Cultures.人雪旺细胞的体外培养II. 传代、纯化、冻存及已建立培养物的标记
Bio Protoc. 2023 Nov 20;13(22):e4882. doi: 10.21769/BioProtoc.4882.
4
The quest for effective immunotherapies against malignant peripheral nerve sheath tumors: Is there hope?寻求针对恶性外周神经鞘瘤的有效免疫疗法:有希望吗?
Mol Ther Oncolytics. 2023 Jul 31;30:227-237. doi: 10.1016/j.omto.2023.07.008. eCollection 2023 Sep 21.
5
Neurofibroma Development in Neurofibromatosis Type 1: Insights from Cellular Origin and Schwann Cell Lineage Development.1型神经纤维瘤病中的神经纤维瘤发生:来自细胞起源和施万细胞谱系发育的见解
Cancers (Basel). 2022 Sep 17;14(18):4513. doi: 10.3390/cancers14184513.
6
Malignant peripheral nerve sheath tumor: models, biology, and translation.恶性外周神经鞘瘤:模型、生物学和转化。
Oncogene. 2022 Apr;41(17):2405-2421. doi: 10.1038/s41388-022-02290-1. Epub 2022 Apr 7.
7
The Role of ER Stress-Related Phenomena in the Biology of Malignant Peripheral Nerve Sheath Tumors.内质网应激相关现象在恶性外周神经鞘瘤生物学中的作用。
Int J Mol Sci. 2021 Aug 30;22(17):9405. doi: 10.3390/ijms22179405.
8
Anti-cancer agent 3-bromopyruvate reduces growth of MPNST and inhibits metabolic pathways in a representative in-vitro model.抗癌剂 3-溴丙酮酸减少 MPNST 的生长,并抑制代表性体外模型中的代谢途径。
BMC Cancer. 2020 Sep 18;20(1):896. doi: 10.1186/s12885-020-07397-w.
9
Motor learning requires myelination to reduce asynchrony and spontaneity in neural activity.运动学习需要髓鞘形成来减少神经活动中的异步性和自发性。
Glia. 2020 Jan;68(1):193-210. doi: 10.1002/glia.23713. Epub 2019 Aug 29.
10
Testing ATRA and MEK inhibitor PD0325901 effectiveness in a nude mouse model for human MPNST xenografts.在人MPNST异种移植裸鼠模型中测试全反式维甲酸(ATRA)和MEK抑制剂PD0325901的有效性。
BMC Res Notes. 2018 Jul 28;11(1):520. doi: 10.1186/s13104-018-3630-0.

本文引用的文献

1
Adenosine: an activity-dependent axonal signal regulating MAP kinase and proliferation in developing Schwann cells.腺苷:一种调节发育中雪旺细胞丝裂原活化蛋白激酶和增殖的活性依赖性轴突信号。
Neuron Glia Biol. 2004 Feb;1(1):23-34. doi: 10.1017/s1740925x04000055.
2
PubMatrix: a tool for multiplex literature mining.PubMatrix:一种用于多重文献挖掘的工具。
BMC Bioinformatics. 2003 Dec 10;4:61. doi: 10.1186/1471-2105-4-61.
3
Receptor-mediated choreography of life and death.受体介导的生死编排。
J Clin Immunol. 2003 Sep;23(5):317-32. doi: 10.1023/a:1025319031417.
4
The role of integrin-linked kinase (ILK) in cancer progression.整合素连接激酶(ILK)在癌症进展中的作用。
Cancer Metastasis Rev. 2003 Dec;22(4):375-84. doi: 10.1023/a:1023777013659.
5
The basement membrane matrix in malignancy.恶性肿瘤中的基底膜基质
J Pathol. 2003 Jul;200(4):465-70. doi: 10.1002/path.1396.
6
Delayed rectifier K currents in NF1 Schwann cells. Pharmacological block inhibits proliferation.1型神经纤维瘤病雪旺细胞中的延迟整流钾电流。药理学阻断抑制增殖。
Neurobiol Dis. 2003 Jul;13(2):136-46. doi: 10.1016/s0969-9961(03)00031-7.
7
P2Y6 nucleotide receptor activates PKC to protect 1321N1 astrocytoma cells against tumor necrosis factor-induced apoptosis.P2Y6核苷酸受体激活蛋白激酶C以保护1321N1星形细胞瘤细胞免受肿瘤坏死因子诱导的凋亡。
Cell Mol Neurobiol. 2003 Jun;23(3):401-18. doi: 10.1023/a:1023696806609.
8
Remodeling of the microenvironment by aggressive melanoma tumor cells.侵袭性黑色素瘤肿瘤细胞对微环境的重塑。
Ann N Y Acad Sci. 2003 May;995:151-61. doi: 10.1111/j.1749-6632.2003.tb03218.x.
9
Neural cell adhesion molecule is upregulated in nerves with prostate cancer invasion.神经细胞黏附分子在受前列腺癌侵袭的神经中上调。
Hum Pathol. 2003 May;34(5):457-61. doi: 10.1016/s0046-8177(03)00084-4.
10
Analysis of microarray data using Z score transformation.使用Z分数转换分析微阵列数据。
J Mol Diagn. 2003 May;5(2):73-81. doi: 10.1016/S1525-1578(10)60455-2.

对一种源自恶性周围神经鞘膜瘤的细胞系和正常人雪旺细胞进行转录谱分析。

Transcriptional profiling in an MPNST-derived cell line and normal human Schwann cells.

作者信息

Lee Philip R, Cohen Jonathan E, Tendi Elisabetta A, Farrer Robert, DE Vries George H, Becker Kevin G, Fields R Douglas

机构信息

Section on Nervous System Development and Plasticity, Bldg. 35, Rm. 2A211, MSC 3713 NICHD, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Neuron Glia Biol. 2004 May;1(2):135-47. doi: 10.1017/s1740925x04000274.

DOI:10.1017/s1740925x04000274
PMID:16429615
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1325299/
Abstract

cDNA microarrays were utilized to identify abnormally expressed genes in a malignant peripheral nerve sheath tumor (MPNST)-derived cell line, T265, by comparing the mRNA abundance profiles with that of normal human Schwann cells (nhSCs). The findings characterize the molecular phenotype of this important cell-line model of MPNSTs, and elucidate the contribution of Schwann cells in MPNSTs. In total, 4608 cDNA sequences were screened and hybridizations replicated on custom cDNA microarrays. In order to verify the microarray data, a large selection of differentially expressed mRNA transcripts were subjected to semi-quantitative reverse transcription PCR (LightCycler). Western blotting was performed to investigate a selection of genes and signal transduction pathways, as a further validation of the microarray data. The data generated from multiple microarray screens, semi-quantitative RT-PCR and Western blotting are in broad agreement. This study represents a comprehensive gene-expression analysis of an MPNST-derived cell line and the first comprehensive global mRNA profile of nhSCs in culture. This study has identified ~900 genes that are expressed abnormally in the T265 cell line and detected many genes not previously reported to be expressed in nhSCs. The results provide crucial information on the T265 cells that is essential for investigation using this cell line in experimental studies in neurofibromatosis type I (NF1), and important information on normal human Schwann cells that is applicable to a wide range of studies on Schwann cells in cell culture.

摘要

通过将恶性外周神经鞘瘤(MPNST)来源的细胞系T265的mRNA丰度谱与正常人雪旺细胞(nhSCs)的进行比较,利用cDNA微阵列来鉴定异常表达的基因。这些发现描绘了MPNST这一重要细胞系模型的分子表型,并阐明了雪旺细胞在MPNST中的作用。总共筛选了4608个cDNA序列,并在定制的cDNA微阵列上重复进行杂交。为了验证微阵列数据,对大量差异表达的mRNA转录本进行了半定量逆转录PCR(LightCycler)。进行蛋白质印迹分析以研究一系列基因和信号转导途径,作为对微阵列数据的进一步验证。多个微阵列筛选、半定量RT-PCR和蛋白质印迹产生的数据基本一致。本研究代表了对MPNST来源的细胞系进行的全面基因表达分析,以及首次对培养中的nhSCs进行的全面全球mRNA谱分析。本研究鉴定出约900个在T265细胞系中异常表达的基因,并检测到许多以前未报道在nhSCs中表达的基因。这些结果提供了关于T265细胞的关键信息,这对于在I型神经纤维瘤病(NF1)的实验研究中使用该细胞系至关重要,同时也提供了关于正常人雪旺细胞的重要信息,适用于细胞培养中关于雪旺细胞的广泛研究。