FGF1 signaling regulates self-renewal of glioblastoma stem cells through activation of aurora a kinase

Chien-Yu Kao, Yi-Chao Hsu, I. Chiu
{"title":"FGF1 signaling regulates self-renewal of glioblastoma stem cells through activation of aurora a kinase","authors":"Chien-Yu Kao, Yi-Chao Hsu, I. Chiu","doi":"10.14800/CCM.1389","DOIUrl":null,"url":null,"abstract":"Glioblastoma (GBM) is a highly malignant brain tumor. The GBM tumor mass contains a unique cell population, GBM stem cells (GBM-SCs), which possess the self-renewal, tumor initiating and tumor progression. FGF1B is the major transcriptional variant of FGF1 in GBM. In our recent study, we demonstrated the FGF1B transcript is up-regulated in self-renewing GBM cells. In order to study GBM-SCs, we developed an approach to isolate GBM-SCs by using FGF1B promoter-driven GFP reporter (F1BGFP). We showed that F1BGFP(+) GBM cells exhibit higher phosphorylation levels of FGFR and AurA than F1BGFP(-) cells, indicating the activation of FGFR and AurA. In this research highlight, we summarized the role of FGF1 signaling and AurA in tumorigenesis. In addition, we also suggested that FGF1-FGFR-AurA cascade regulates GBM-SCs, which may enable development of target-based therapy that act against the GBM-SCs.","PeriodicalId":9576,"journal":{"name":"Cancer cell & microenvironment","volume":"80 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer cell & microenvironment","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14800/CCM.1389","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Glioblastoma (GBM) is a highly malignant brain tumor. The GBM tumor mass contains a unique cell population, GBM stem cells (GBM-SCs), which possess the self-renewal, tumor initiating and tumor progression. FGF1B is the major transcriptional variant of FGF1 in GBM. In our recent study, we demonstrated the FGF1B transcript is up-regulated in self-renewing GBM cells. In order to study GBM-SCs, we developed an approach to isolate GBM-SCs by using FGF1B promoter-driven GFP reporter (F1BGFP). We showed that F1BGFP(+) GBM cells exhibit higher phosphorylation levels of FGFR and AurA than F1BGFP(-) cells, indicating the activation of FGFR and AurA. In this research highlight, we summarized the role of FGF1 signaling and AurA in tumorigenesis. In addition, we also suggested that FGF1-FGFR-AurA cascade regulates GBM-SCs, which may enable development of target-based therapy that act against the GBM-SCs.
FGF1信号通过激活极光激酶调节胶质母细胞瘤干细胞的自我更新
胶质母细胞瘤是一种高度恶性的脑肿瘤。GBM肿瘤团块包含一种独特的细胞群——GBM干细胞(GBM- scs),它具有自我更新、肿瘤启动和肿瘤进展的能力。FGF1B是GBM中FGF1的主要转录变体。在我们最近的研究中,我们证明了FGF1B转录物在自我更新的GBM细胞中上调。为了研究GBM-SCs,我们开发了一种利用FGF1B启动子驱动的GFP报告基因(F1BGFP)分离GBM-SCs的方法。我们发现F1BGFP(+) GBM细胞比F1BGFP(-)细胞表现出更高的FGFR和AurA磷酸化水平,表明FGFR和AurA被激活。在本研究重点中,我们总结了FGF1信号和AurA在肿瘤发生中的作用。此外,我们还提出FGF1-FGFR-AurA级联调节GBM-SCs,这可能促进针对GBM-SCs的靶向治疗的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信