Targeting DNM1L/DRP1-FIS1 axis inhibits high-grade glioma progression by impeding mitochondrial respiratory cristae remodeling

This study highlights that the DNM1L/DRP1-FIS1 axis stabilizes MRC structures through mitophagy in HGG cells while driving their OXPHOS activity ultimately leading to robust disease progression. The inhibition of the DNM1L/DRP1-FIS1 axis hinders MRC remodeling and suppresses GBM progression. We propose that down-regulation of the DNM1L/DRP1-FIS1 axis could be a potential therapeutic strategy for treating HGG.

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Publication Details

Journal
Journal of Experimental & Clinical Cancer Research
Published
2024-09-30
DOI
https://doi.org/10.1186/s13046-024-03194-6
Citations
18
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
4.21
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article

Targeting DNM1L/DRP1-FIS1 axis inhibits high-grade glioma progression by impeding mitochondrial respiratory cristae remodeling

Q. Guo, Shi‐Zhou Deng, Yayun Wang, C Gong et al.
18 citations
Journal of Experimental & Clinical Cancer Research
Mitochondrial Function and Pathology
4.21
article

Targeting DNM1L/DRP1-FIS1 axis inhibits high-grade glioma progression by impeding mitochondrial respiratory cristae remodeling

Q. Guo, Shi‐Zhou Deng, Yayun Wang, C Gong, Yanling Yang, Y Wang, Guopeng Zhang, Shujiao Li, Yuze Sun, Hui Liu, Zhenhua Wang, Jing-Jing Tie, Feifei Wu, Xiaodong Li, Yousheng Wu, Xiyu Chen
article en
18 citations

Abstract

This study highlights that the DNM1L/DRP1-FIS1 axis stabilizes MRC structures through mitophagy in HGG cells while driving their OXPHOS activity ultimately leading to robust disease progression. The inhibition of the DNM1L/DRP1-FIS1 axis hinders MRC remodeling and suppresses GBM progression. We propose that down-regulation of the DNM1L/DRP1-FIS1 axis could be a potential therapeutic strategy for treating HGG.

Journal of Experimental & Clinical Cancer ResearchVol. 43(1)
Yan'an University (CN), Air Force Medical University (CN)
Life below water
Openalex Percentile: Top 5%
Mitochondrial Function and Pathology
4.21
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