Nootkatone inhibits the progression of glioblastoma by activating the ATF4-CHOP-CHAC1 pathway.

IF 6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Medicine Pub Date : 2025-01-16 DOI:10.1186/s10020-025-01064-1
Qian Wang, Xiumin Xue, Zhichao Chen, Wei Zhang, Yiming Qian, Danni Chen, Lin Lin, Yinfeng Yuan, Weiqiao Zhao, Zhihui Huang, Yongjie Wang
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Abstract

Glioblastoma multiforme (GBM) represents a primary brain tumor that is widely prevalent, and clinical drugs available for its treatment exhibit varying degrees of resistance. Nootkatone (NKT) is a functional sesquiterpene sourced from traditional Chinese medicine --Alpinia Oxyphylla Miq and has been reported to have a diverse range of pharmacological properties. However, it remains unknown whether there are effects of NKT on GBM. In this study, we found that NKT inhibited the growth of GBM cells in a dose-dependent manner in vitro. Subsequently, we observed that NKT suppressed the migration and arrested cell cycle at G2/M phase of GBM cells. Furthermore, NKT induced the death of GBM cells accompanied by an increase in reactive oxygen species (ROS) production. Mechanistically, we found that NKT inhibited the progression of GBM cells through activating the ATF4-CHOP-CHAC1 pathway in GBM cells. Furthermore, NKT-induced inhibition of migration and proliferation in GBM cells was partially restored by ATF4 or CHAC1 knockdown. Finally, we found that NKT inhibited the growth of tumor in GBM orthotopic mice model through activation of ATF4-CHOP-CHAC1 axis. Taken together, our findings show that NKT suppresses the growth and migration of GBM cells by activating the ATF4-CHOP-CHAC1 pathway, which in turn prevents the tumorigenesis of GBMs and provides a novel perspective for the development of drugs against GBM.

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诺卡酮通过激活ATF4-CHOP-CHAC1通路抑制胶质母细胞瘤的进展。
多形性胶质母细胞瘤(GBM)是一种广泛流行的原发性脑肿瘤,其临床治疗药物表现出不同程度的耐药性。Nootkatone (NKT)是一种功能性倍半萜,来源于传统中药——Alpinia Oxyphylla Miq,据报道具有多种药理特性。然而,目前尚不清楚NKT是否对GBM有影响。在本研究中,我们发现NKT在体外以剂量依赖性方式抑制GBM细胞的生长。随后,我们观察到NKT抑制了GBM细胞的迁移,并在G2/M期阻滞了细胞周期。此外,NKT诱导GBM细胞死亡,并伴有活性氧(ROS)产生的增加。在机制上,我们发现NKT通过激活GBM细胞中的ATF4-CHOP-CHAC1通路来抑制GBM细胞的进展。此外,通过敲除ATF4或CHAC1,可以部分恢复nkt诱导的GBM细胞迁移和增殖抑制。最后,我们发现NKT通过激活ATF4-CHOP-CHAC1轴抑制GBM原位小鼠模型的肿瘤生长。综上所述,我们的研究结果表明,NKT通过激活ATF4-CHOP-CHAC1通路来抑制GBM细胞的生长和迁移,从而阻止GBM的肿瘤发生,并为开发抗GBM药物提供了新的视角。
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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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