铜转运蛋白1介导的铜死亡途径及其在肿瘤治疗中的潜在价值
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:

国家自然科学基金(82473565),海军军医大学校级基础医学研究课题(2024QN017).


Role of copper transporter 1 in regulating cuproptosis and its potential value in tumor therapy
Author:
Affiliation:

Fund Project:

Supported by National Natural Science Foundation of China (82473565) and Basic Medical Research Project of Naval Medical University (2024QN017).

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    作为一种独特的细胞死亡方式,铜死亡的发生取决于细胞内铜离子的累积。铜离子是生物体内正常生理状态下的必需微量元素,但细胞内过量的游离铜不仅对正常细胞产生毒性作用,还会对肿瘤细胞发挥特异性杀伤功能。铜转运蛋白1(CTR1)是细胞跨膜摄取铜离子的关键转运体,作为一种铜死亡调节因子,其在肿瘤中的突变及表达变化对铜离子在细胞内外的分布有影响,并可能通过调控铜死亡途径参与肿瘤细胞增殖、侵袭、迁移等多个生物学过程。本文对CTR1介导的铜死亡途径及其在肿瘤治疗中的潜在价值进行综述,阐述铜离子稳态调控机制对生物体完成正常生命活动的重要性及CTR1调控铜死亡的机制,并探讨以CTR1为干预靶点进行肿瘤治疗的潜在价值,为临床肿瘤患者的救治提供新的研究方向。

    Abstract:

    As a new manner of cell death, cuproptosis depends on the accumulation of copper ions in cells. Copper ion is an essential trace element in normal physiological state of organisms. The excess of free copper in cells not only has toxic effect on normal cells, but also plays its specific killing function on tumor cells. Copper transporter 1 (CTR1) is a key transporter of transmembrane uptake of copper ions by cells. As a regulator of cuproptosis, its mutation and expression changes in tumors have an impact on the distribution of copper ions inside and outside the cells. It may participate in multiple biological processes such as proliferation, invasion and migration of tumor cells by regulating the pathway of cuproptosis. This article reviews the cuproptosis pathway mediated by CTR1 and the potential value of CTR1 in tumor treatment, elaborates the importance of copper ion homeostasis regulation for normal life activities and the mechanism of CTR1 in regulating cuproptosis, and discusses the potential value of CTR1 as a new target for tumor therapy, so as to provide a theoretical basis for the treatment of tumor patients.

    参考文献
    相似文献
    引证文献
相关视频

分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2024-11-21
  • 最后修改日期:2024-12-26
  • 录用日期:
  • 在线发布日期: 2025-08-19
  • 出版日期: 2025-08-20
文章二维码
重要通知
友情提醒: 近日发现论文正式见刊或网络首发后,有人冒充我刊编辑部名义给作者发邮件,要求添加微信,此系诈骗行为!可致电编辑部核实:021-81870792。
            《海军军医大学学报》编辑部
关闭