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依伐卡托抑制胶质母细胞瘤干细胞维持和肿瘤进展。

Ivacaftor Inhibits Glioblastoma Stem Cell Maintenance and Tumor Progression.

作者信息

Liu Kun, Pu Jun, Nie Zhi, Shi Yulin, Jiang Liping, Wu Qisheng, Chen Yongbin, Yang Cuiping

机构信息

Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences and Yunnan Province, Kunming Institute of Zoology, Kunming, China.

Kunming College of Life Science, University of Chinese Academy of Sciences, Beijing, China.

出版信息

Front Cell Dev Biol. 2021 May 11;9:678209. doi: 10.3389/fcell.2021.678209. eCollection 2021.

Abstract

Glioblastoma (GBM) is the most common and malignant primary brain tumor. Glioblastoma stem cells (GSCs) not only initiate and sustain uncontrolled cell proliferation but also resistant to conventional clinical therapies including temozolomide (TMZ) dependent chemotherapy and radiotherapy, implying that there is an urgent need to identify new therapeutic strategies especially specific targeting GSCs. Here, we provide evidence showing that ivacaftor commonly applied in cystic fibrosis therapy acts as a potent inhibitor for GSCs maintenance. We found that ivacaftor promotes cellular apoptosis and represses patient-derived xenograft (PDX) tumor growth . In addition, we demonstrate that ivacaftor decreases stemness marker gene expressions of GSCs, including CD133, CD44, and Sox2. In summary, our findings reveal that ivacaftor inhibits glioblastoma progression via specifically eliminating GSCs, which opens a new avenue for GBM clinical therapy in the future.

摘要

胶质母细胞瘤(GBM)是最常见且恶性程度最高的原发性脑肿瘤。胶质母细胞瘤干细胞(GSCs)不仅启动并维持不受控制的细胞增殖,还对包括替莫唑胺(TMZ)依赖的化疗和放疗在内的传统临床治疗产生抗性,这意味着迫切需要确定新的治疗策略,尤其是特异性靶向GSCs的策略。在此,我们提供证据表明,常用于囊性纤维化治疗的依伐卡托可作为GSCs维持的有效抑制剂。我们发现依伐卡托可促进细胞凋亡并抑制患者来源异种移植(PDX)肿瘤的生长。此外,我们证明依伐卡托可降低GSCs的干性标记基因表达,包括CD133、CD44和Sox2。总之,我们的研究结果表明依伐卡托通过特异性消除GSCs来抑制胶质母细胞瘤的进展,这为未来GBM的临床治疗开辟了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08e2/8147559/14e6847e7c28/fcell-09-678209-g001.jpg

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