首页 / 院系成果 / 成果详情页

NSD1 mutation status determines metabolic inhibitor sensitivity in head and neck squamous cell carcinomas by regulating mitochondrial respiration  期刊论文  

  • 编号:
    4E31DC18437155C7992589FE0A3F51C5
  • 作者:
    Tang, Shouyi(唐守毅)#[1,2]Wang, Qing#[1]Wang, Zhen[1];Cai, Luyao[1];Pan, Dan[1];Li, Jing[1];Chen, Qianming[1];Zhou, Yu*[1]Shen, YingQiang*[1]
  • 语种:
    英文
  • 期刊:
    JOURNAL OF PATHOLOGY ISSN:0022-3417 2025 年 266 卷 3 期 (306 - 321) ; JUL
  • 收录:
  • 关键词:
  • 摘要:

    Head and neck squamous cell carcinomas (HNSCCs) are the most common malignant tumors in the head and neck region, characterized by a high recurrence rate and early metastasis. Despite advances in treatment, patient outcomes and prognosis remain poor, highlighting the urgent need for new therapeutic strategies. Recent research has increasingly focused on targeting glucose metabolism as a therapeutic strategy for cancer, revealing multiple promising targets and potential drugs. However, the metabolic heterogeneity among tumors leads to variable sensitivity to metabolic inhibitors in different patients, limiting their clinical utility. In this study, we employed bioinformatics analysis, cell experiments, animal models, and multi-omics approaches to reveal differences in glucose metabolism phenotypes among HNSCC patients and elucidated the underlying molecular mechanisms driving these differences. Our findings showed that NSD1 mutation status affects the glucose metabolism phenotype in HNSCC, with NSD1 wild-type HNSCC exhibiting higher mitochondrial respiration and NSD1 mutant HNSCC showing weaker mitochondrial respiration but enhanced glycolysis. We further demonstrated that NSD1 regulates mitochondrial respiration in HNSCC via epigenetic modulation of the TGFB2/PPARGC1A signaling axis. Additionally, we found that NSD1 wild-type HNSCC is more sensitive to mitochondrial respiration inhibitors, whereas NSD1 mutant HNSCC shows increased sensitivity to glycolysis inhibitors. In summary, we found that NSD1 can epigenetically regulate the TGFB2/PPARGC1A axis to modulate mitochondrial respiration and sensitivity to metabolic inhibitors in HNSCC. These findings suggest a novel strategy for selecting metabolic inhibitors for HNSCC based on the NSD1 gene status of patients. (c) 2025 The Pathological Society of Great Britain and Ireland.

  • 推荐引用方式
    GB/T 7714:
    Tang Shouyi,Wang Qing,Wang Zhen, et al. NSD1 mutation status determines metabolic inhibitor sensitivity in head and neck squamous cell carcinomas by regulating mitochondrial respiration [J].JOURNAL OF PATHOLOGY,2025,266(3):306-321.
  • APA:
    Tang Shouyi,Wang Qing,Wang Zhen,Cai Luyao,&Shen Ying-Qiang.(2025).NSD1 mutation status determines metabolic inhibitor sensitivity in head and neck squamous cell carcinomas by regulating mitochondrial respiration .JOURNAL OF PATHOLOGY,266(3):306-321.
  • MLA:
    Tang Shouyi, et al. "NSD1 mutation status determines metabolic inhibitor sensitivity in head and neck squamous cell carcinomas by regulating mitochondrial respiration" .JOURNAL OF PATHOLOGY 266,3(2025):306-321.
  • 入库时间:
    2025/7/3 21:43:56
  • 更新时间:
    2025/7/4 0:07:58
  • 条目包含文件:
    文件类型: , 文件大小:
    正在加载全文
浏览次数:51 下载次数:0
浏览次数:51
下载次数:0
打印次数:0
浏览器支持: Google Chrome   火狐   360浏览器极速模式(8.0+极速模式) 
返回顶部