• 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

在一种新的原代细胞系上进行药物重新定位筛选,确定了胶质母细胞瘤的有效治疗方法。

Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma.

作者信息

Senbabaoglu Filiz, Aksu Ali Cenk, Cingoz Ahmet, Seker-Polat Fidan, Borklu-Yucel Esra, Solaroglu İhsan, Bagci-Onder Tugba

机构信息

Brain Cancer Research and Therapy Laboratory, Koç University School of Medicine, Istanbul, Turkey.

Koç University Research Center for Translational Medicine, Istanbul, Turkey.

出版信息

Front Neurosci. 2020 Dec 17;14:578316. doi: 10.3389/fnins.2020.578316. eCollection 2020.

DOI:10.3389/fnins.2020.578316
PMID:33390879
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7773901/
Abstract

Glioblastoma is a malignant brain cancer with limited treatment options and high mortality rate. While established glioblastoma cell line models provide valuable information, they ultimately lose most primary characteristics of tumors under long-term serum culture conditions. Therefore, established cell lines do not necessarily recapitulate genetic and morphological characteristics of real tumors. In this study, in line with the growing interest in using primary cell line models derived from patient tissue, we generated a primary glioblastoma cell line, KUGBM8 and characterized its genetic alterations, long term growth ability, tumor formation capacity and its response to Temozolomide, the front-line chemotherapy utilized clinically. In addition, we performed a drug repurposing screen on the KUGBM8 cell line to identify FDA-approved agents that can be incorporated into glioblastoma treatment regimen and identified Topotecan as a lead drug among 1,200 drugs. We showed Topotecan can induce cell death in KUGBM8 and other primary cell lines and cooperate with Temozolomide in low dosage combinations. Together, our study provides a new primary cell line model that can be suitable for both and studies and suggests that Topotecan can offer promise as a therapeutic approach for glioblastoma.

摘要

胶质母细胞瘤是一种恶性脑癌,治疗选择有限且死亡率高。虽然已建立的胶质母细胞瘤细胞系模型提供了有价值的信息,但在长期血清培养条件下,它们最终会失去肿瘤的大多数原发特征。因此,已建立的细胞系不一定能重现真实肿瘤的遗传和形态特征。在本研究中,随着对使用源自患者组织的原代细胞系模型的兴趣日益增加,我们建立了一种原代胶质母细胞瘤细胞系KUGBM8,并对其遗传改变、长期生长能力、肿瘤形成能力以及对临床上一线化疗药物替莫唑胺的反应进行了表征。此外,我们对KUGBM8细胞系进行了药物再利用筛选,以确定可纳入胶质母细胞瘤治疗方案的FDA批准药物,并在1200种药物中确定拓扑替康为先导药物。我们表明,拓扑替康可诱导KUGBM8和其他原代细胞系中的细胞死亡,并在低剂量组合中与替莫唑胺协同作用。总之,我们的研究提供了一种新的原代细胞系模型,该模型适用于[此处原文缺失两个并列的内容]研究,并表明拓扑替康有望成为胶质母细胞瘤的一种治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/79cbf8fd1262/fnins-14-578316-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/f7bbbe6fbb0b/fnins-14-578316-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/acf20a26ef22/fnins-14-578316-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/cbdd1a5756a0/fnins-14-578316-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/7303e292e217/fnins-14-578316-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/79cbf8fd1262/fnins-14-578316-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/f7bbbe6fbb0b/fnins-14-578316-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/acf20a26ef22/fnins-14-578316-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/cbdd1a5756a0/fnins-14-578316-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/7303e292e217/fnins-14-578316-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a7/7773901/79cbf8fd1262/fnins-14-578316-g005.jpg

相似文献

1
Drug Repositioning Screen on a New Primary Cell Line Identifies Potent Therapeutics for Glioblastoma.在一种新的原代细胞系上进行药物重新定位筛选,确定了胶质母细胞瘤的有效治疗方法。
Front Neurosci. 2020 Dec 17;14:578316. doi: 10.3389/fnins.2020.578316. eCollection 2020.
2
Disulfiram when Combined with Copper Enhances the Therapeutic Effects of Temozolomide for the Treatment of Glioblastoma.二硫化物与铜联合增强替莫唑胺治疗胶质母细胞瘤的疗效。
Clin Cancer Res. 2016 Aug 1;22(15):3860-75. doi: 10.1158/1078-0432.CCR-15-1798. Epub 2016 Mar 22.
3
Drug repositioning of antiretroviral ritonavir for combinatorial therapy in glioblastoma.抗逆转录病毒药物利托那韦的药物重定位用于胶质母细胞瘤的联合治疗。
Eur J Cancer. 2020 Nov;140:130-139. doi: 10.1016/j.ejca.2020.09.017. Epub 2020 Oct 19.
4
Thioridazine inhibits autophagy and sensitizes glioblastoma cells to temozolomide.硫利达嗪抑制自噬并增强胶质母细胞瘤细胞对替莫唑胺的敏感性。
Int J Cancer. 2019 Apr 1;144(7):1735-1745. doi: 10.1002/ijc.31912. Epub 2018 Dec 11.
5
Recycling drug screen repurposes hydroxyurea as a sensitizer of glioblastomas to temozolomide targeting de novo DNA synthesis, irrespective of molecular subtype.药物再利用筛选将羟基脲重新用作替莫唑胺增敏剂,针对新合成的 DNA,而与分子亚型无关。
Neuro Oncol. 2018 Apr 9;20(5):642-654. doi: 10.1093/neuonc/nox198.
6
Use of an anti-viral drug, Ribavirin, as an anti-glioblastoma therapeutic.使用抗病毒药物利巴韦林作为胶质母细胞瘤的治疗方法。
Oncogene. 2017 May 25;36(21):3037-3047. doi: 10.1038/onc.2016.457. Epub 2016 Dec 12.
7
Mechanisms and Antitumor Activity of a Binary EGFR/DNA-Targeting Strategy Overcomes Resistance of Glioblastoma Stem Cells to Temozolomide.二元 EGFR/DNA 靶向策略的机制和抗肿瘤活性克服胶质母细胞瘤干细胞对替莫唑胺的耐药性。
Clin Cancer Res. 2019 Dec 15;25(24):7594-7608. doi: 10.1158/1078-0432.CCR-19-0955. Epub 2019 Sep 20.
8
Repurposing drugs for glioblastoma: From bench to bedside.胶质母细胞瘤药物再利用:从基础到临床。
Cancer Lett. 2018 Aug 1;428:173-183. doi: 10.1016/j.canlet.2018.04.039. Epub 2018 May 3.
9
Investigating a signature of temozolomide resistance in GBM cell lines using metabolomics.利用代谢组学研究胶质母细胞瘤细胞系中替莫唑胺耐药的特征。
J Neurooncol. 2015 Oct;125(1):91-102. doi: 10.1007/s11060-015-1899-6. Epub 2015 Aug 28.
10
In vitro evaluation of combined temozolomide and radiotherapy using X  rays and high-linear energy transfer radiation for glioblastoma.体外评估替莫唑胺联合放疗治疗胶质母细胞瘤的研究:X 射线与高线性能量转移射线的比较。
Radiat Res. 2012 May;177(5):651-62. doi: 10.1667/rr2803.1. Epub 2012 Apr 2.

引用本文的文献

1
Opportunities and challenges for patient-derived models of brain tumors in functional precision medicine.功能性精准医学中脑肿瘤患者衍生模型的机遇与挑战
NPJ Precis Oncol. 2025 Feb 14;9(1):47. doi: 10.1038/s41698-025-00832-w.
2
Enhanced Cytotoxic Effects of Cold Plasma Deposition of Topotecan: A Novel Approach for Local Cancer Drug Delivery to Glioblastoma Cells.拓扑替康冷等离子体沉积增强的细胞毒性作用:一种向胶质母细胞瘤细胞进行局部癌症药物递送的新方法。
Cancers (Basel). 2025 Jan 9;17(2):201. doi: 10.3390/cancers17020201.
3
Chronically Radiation-Exposed Survivor Glioblastoma Cells Display Poor Response to Chk1 Inhibition under Hypoxia.

本文引用的文献

1
Clinical exome sequencing in neuromuscular diseases: an experience from Turkey.神经肌肉疾病的临床外显子组测序:来自土耳其的经验。
Neurol Sci. 2020 Aug;41(8):2157-2164. doi: 10.1007/s10072-020-04304-w. Epub 2020 Mar 5.
2
Cell Culture Medium Formulation and Its Implications in Cancer Metabolism.细胞培养基配方及其在癌症代谢中的意义。
Trends Cancer. 2019 Jun;5(6):329-332. doi: 10.1016/j.trecan.2019.05.004. Epub 2019 May 29.
3
Temozolomide resistance in glioblastoma multiforme.多形性胶质母细胞瘤中的替莫唑胺耐药性。
慢性辐射暴露的胶质母细胞瘤细胞在低氧条件下对 Chk1 抑制的反应较差。
Int J Mol Sci. 2022 Jun 24;23(13):7051. doi: 10.3390/ijms23137051.
Genes Dis. 2016 May 11;3(3):198-210. doi: 10.1016/j.gendis.2016.04.007. eCollection 2016 Sep.
4
Culture conditions defining glioblastoma cells behavior: what is the impact for novel discoveries?定义胶质母细胞瘤细胞行为的培养条件:对新发现有何影响?
Oncotarget. 2017 Aug 11;8(40):69185-69197. doi: 10.18632/oncotarget.20193. eCollection 2017 Sep 15.
5
Topotecan is a potent inhibitor of SUMOylation in glioblastoma multiforme and alters both cellular replication and metabolic programming.拓扑替康是多形性胶质母细胞瘤中 SUMOylation 的有效抑制剂,可改变细胞复制和代谢编程。
Sci Rep. 2017 Aug 7;7(1):7425. doi: 10.1038/s41598-017-07631-9.
6
Drug repurposing from the perspective of pharmaceutical companies.从制药公司的角度看药物再利用。
Br J Pharmacol. 2018 Jan;175(2):168-180. doi: 10.1111/bph.13798. Epub 2017 May 18.
7
Anthelmintic drug ivermectin inhibits angiogenesis, growth and survival of glioblastoma through inducing mitochondrial dysfunction and oxidative stress.抗寄生虫药物伊维菌素通过诱导线粒体功能障碍和氧化应激来抑制胶质母细胞瘤的血管生成、生长和存活。
Biochem Biophys Res Commun. 2016 Nov 18;480(3):415-421. doi: 10.1016/j.bbrc.2016.10.064. Epub 2016 Oct 19.
8
Suppression of the Eag1 potassium channel sensitizes glioblastoma cells to injury caused by temozolomide.Eag1钾通道的抑制使胶质母细胞瘤细胞对替莫唑胺引起的损伤敏感。
Oncol Lett. 2016 Oct;12(4):2581-2589. doi: 10.3892/ol.2016.4992. Epub 2016 Aug 10.
9
Targeted sequencing of refractory myeloma reveals a high incidence of mutations in CRBN and Ras pathway genes.难治性骨髓瘤的靶向测序显示CRBN和Ras信号通路基因的突变发生率很高。
Blood. 2016 Sep 1;128(9):1226-33. doi: 10.1182/blood-2016-02-698092. Epub 2016 Jul 25.
10
Identification of Mitoxantrone as a TRAIL-sensitizing agent for Glioblastoma Multiforme.米托蒽醌作为多形性胶质母细胞瘤的TRAIL增敏剂的鉴定。
Cancer Biol Ther. 2016 May 3;17(5):546-57. doi: 10.1080/15384047.2016.1167292. Epub 2016 Mar 30.