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1
Clinically relevant doses of chemotherapy agents reversibly block formation of glioblastoma neurospheres.临床相关剂量的化疗药物可可逆地阻断神经球的形成。
Cancer Lett. 2010 Oct 28;296(2):168-77. doi: 10.1016/j.canlet.2010.04.005.
2
[Temozolomide in patients with a glioblastoma multiforme: new developments].[替莫唑胺治疗多形性胶质母细胞瘤患者:新进展]
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3
O6-benzylguanine enhances the sensitivity of a glioma xenograft with low O6-alkylguanine-DNA alkyltransferase activity to temozolomide and BCNU.O6-苄基鸟嘌呤增强了具有低O6-烷基鸟嘌呤-DNA烷基转移酶活性的胶质瘤异种移植瘤对替莫唑胺和卡莫司汀的敏感性。
Br J Cancer. 1996 May;73(9):1049-52. doi: 10.1038/bjc.1996.203.
4
Salvage chemotherapy with cyclophosphamide for recurrent, temozolomide-refractory glioblastoma multiforme.环磷酰胺挽救性化疗用于复发性、对替莫唑胺耐药的多形性胶质母细胞瘤。
Cancer. 2004 Mar 15;100(6):1213-20. doi: 10.1002/cncr.20072.
5
Promising survival and concomitant radiation plus temozolomide followed by adjuvant temozolomide.有前景的生存情况以及同步放疗加替莫唑胺,随后进行辅助性替莫唑胺治疗。
J Clin Oncol. 2002 Jul 15;20(14):3180-1; author reply 3181. doi: 10.1200/JCO.2002.20.14.3180.
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Adjuvant temozolomide: how long and how much?辅助性替莫唑胺:疗程多久及剂量多少?
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Prospective study of carmustine wafers in combination with 6-month metronomic temozolomide and radiation therapy in newly diagnosed glioblastoma: preliminary results.新诊断的胶质母细胞瘤中卡莫司汀植入剂联合 6 个月节拍式替莫唑胺和放疗的前瞻性研究:初步结果。
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Fluids Barriers CNS. 2018 Jan 15;15(1):2. doi: 10.1186/s12987-017-0088-8.
10
Treatment of brain tumors.脑肿瘤的治疗。
N Engl J Med. 2005 Jun 2;352(22):2350-3; author reply 2350-3.

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Mismatch repair proteins play a role in ATR activation upon temozolomide treatment in MGMT-methylated glioblastoma.错配修复蛋白在 MGMT 甲基化胶质母细胞瘤经替莫唑胺治疗后 ATR 的激活中发挥作用。
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Inhibitors of GLUT/SLC2A Enhance the Action of BCNU and Temozolomide against High-Grade Gliomas.葡萄糖转运蛋白/溶质载体家族2成员A(GLUT/SLC2A)抑制剂增强卡莫司汀和替莫唑胺对高级别胶质瘤的作用。
Neoplasia. 2017 Apr;19(4):364-373. doi: 10.1016/j.neo.2017.02.009. Epub 2017 Mar 19.
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Humanized chondroitinase ABC sensitizes glioblastoma cells to temozolomide.人源化软骨素酶ABC使胶质母细胞瘤细胞对替莫唑胺敏感。
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7
Patient-derived glioblastoma stem cells respond differentially to targeted therapies.患者来源的胶质母细胞瘤干细胞对靶向治疗反应不同。
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8
A Comparative Study of Survival Rate in High Grade Glioma Tumors Being Treated by Radiotherapy Alone Versus Chemoradiation With Nitrosourea.单纯放疗与亚硝基脲放化疗治疗高级别胶质瘤肿瘤生存率的比较研究
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The DNA damage/repair cascade in glioblastoma cell lines after chemotherapeutic agent treatment.化疗药物处理后胶质母细胞瘤细胞系中的DNA损伤/修复级联反应。
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10
Variant allele frequency enrichment analysis in vitro reveals sonic hedgehog pathway to impede sustained temozolomide response in GBM.体外变异等位基因频率富集分析显示,音猬因子信号通路会阻碍胶质母细胞瘤对替莫唑胺的持续反应。
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本文引用的文献

1
Brain Tumor Stem-Like Cells Identified by Neural Stem Cell Marker CD15.通过神经干细胞标志物 CD15 鉴定脑肿瘤干细胞样细胞。
Transl Oncol. 2009 Dec;2(4):247-57. doi: 10.1593/tlo.09136.
2
Cancer stem cells: cell culture, markers, and targets for new therapies.癌症干细胞:细胞培养、标志物和新疗法靶点。
J Cell Biochem. 2009 Dec 1;108(5):1031-8. doi: 10.1002/jcb.22350.
3
CD133 expression is not selective for tumor-initiating or radioresistant cell populations in the CRC cell lines HCT-116.CD133 表达并不选择性地针对 CRC 细胞系 HCT-116 中的肿瘤起始或放射抵抗细胞群体。
Radiother Oncol. 2009 Sep;92(3):353-61. doi: 10.1016/j.radonc.2009.06.034. Epub 2009 Aug 21.
4
STAT3 is required for proliferation and maintenance of multipotency in glioblastoma stem cells.STAT3 对于神经胶质瘤干细胞的增殖和多能性维持是必需的。
Stem Cells. 2009 Oct;27(10):2383-92. doi: 10.1002/stem.185.
5
CD133 (Prominin) negative human neural stem cells are clonogenic and tripotent.CD133(Prominin)阴性的人类神经干细胞具有克隆能力且具备三向分化潜能。
PLoS One. 2009;4(5):e5498. doi: 10.1371/journal.pone.0005498. Epub 2009 May 11.
6
SSEA-1 is an enrichment marker for tumor-initiating cells in human glioblastoma.SSEA-1是人类胶质母细胞瘤中肿瘤起始细胞的富集标志物。
Cell Stem Cell. 2009 May 8;4(5):440-52. doi: 10.1016/j.stem.2009.03.003.
7
How powerful is CD133 as a cancer stem cell marker in brain tumors?CD133作为脑肿瘤中癌症干细胞标志物的作用有多强大?
Cancer Treat Rev. 2009 Aug;35(5):403-8. doi: 10.1016/j.ctrv.2009.03.002. Epub 2009 Apr 14.
8
Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial.同步放化疗联合辅助替莫唑胺与单纯放疗对胶质母细胞瘤生存影响的随机III期研究:EORTC-NCIC试验的5年分析
Lancet Oncol. 2009 May;10(5):459-66. doi: 10.1016/S1470-2045(09)70025-7. Epub 2009 Mar 9.
9
A2B5 cells from human glioblastoma have cancer stem cell properties.人胶质母细胞瘤 A2B5 细胞具有癌症干细胞特性。
Brain Pathol. 2010 Jan;20(1):211-21. doi: 10.1111/j.1750-3639.2009.00269.x. Epub 2009 Feb 20.
10
Spheroid-based drug screen: considerations and practical approach.基于球体的药物筛选:注意事项及实用方法
Nat Protoc. 2009;4(3):309-24. doi: 10.1038/nprot.2008.226. Epub 2009 Feb 12.

临床相关剂量的化疗药物可可逆地阻断神经球的形成。

Clinically relevant doses of chemotherapy agents reversibly block formation of glioblastoma neurospheres.

机构信息

Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, USA.

出版信息

Cancer Lett. 2010 Oct 28;296(2):168-77. doi: 10.1016/j.canlet.2010.04.005.

DOI:10.1016/j.canlet.2010.04.005
PMID:20435409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2914162/
Abstract

Glioblastoma patients have a poor prognosis, even after surgery, radiotherapy, and chemotherapy with temozolomide or 1,3-bis(2-chloroethy)-1-nitrosourea. We developed an in vitro recovery model using neurosphere cultures to analyze the efficacy of chemotherapy treatments, and tested whether glioblastoma neurosphere-initiating cells are resistant. Concentrations of chemotherapy drugs that inhibit neurosphere formation are similar to clinically relevant doses. Some lines underwent a transient cell cycle arrest and a robust recovery of neurosphere formation. These results indicate that glioblastoma neurospheres can regrow after treatment with chemotherapy drugs. This neurosphere recovery assay will facilitate studies of chemo-resistant subpopulations and methods to enhance glioblastoma therapy.

摘要

胶质母细胞瘤患者预后不良,即使经过手术、放疗和替莫唑胺或 1,3-双(2-氯乙基)-1-亚硝脲化疗也是如此。我们使用神经球培养物开发了一种体外恢复模型,以分析化疗治疗的效果,并测试胶质母细胞瘤神经球起始细胞是否具有耐药性。抑制神经球形成的化疗药物浓度与临床相关剂量相似。一些细胞系经历了短暂的细胞周期停滞和神经球形成的强烈恢复。这些结果表明,胶质母细胞瘤神经球在化疗药物治疗后可以重新生长。这种神经球恢复测定法将有助于研究化疗耐药亚群和增强胶质母细胞瘤治疗的方法。