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鸟瞰肿瘤中线粒体未折叠蛋白反应:机制、进展与进一步应用。

A bird's eye view of mitochondrial unfolded protein response in cancer: mechanisms, progression and further applications.

机构信息

Ministry of Education Key Laboratory of Molecular and Cellular Biology; Hebei Research Center of the Basic Discipline of Cell Biology, Hebei Collaborative Innovation Center for Eco-Environment, Hebei Province Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, College of Life Sciences, Hebei Normal University, Shijiazhuang, Hebei, China.

出版信息

Cell Death Dis. 2024 Sep 11;15(9):667. doi: 10.1038/s41419-024-07049-y.

Abstract

Mitochondria are essential organelles that play critical roles in energy metabolism, apoptosis and various cellular processes. Accumulating evidence suggests that mitochondria are also involved in cancer development and progression. The mitochondrial unfolded protein response (UPR) is a complex cellular process that is activated when the protein-folding capacity of the mitochondria is overwhelmed. The core machinery of UPR includes upstream regulatory factors, mitochondrial chaperones and proteases. These components work together to eliminate misfolded proteins, increase protein-folding capacity, and restore mitochondrial function. Recent studies have shown that UPR is dysregulated in various cancers and contributes to tumor initiation, growth, metastasis, and therapeutic resistance. Considering the pivotal role of the UPR in oncogenesis, numerous compounds and synthetic drugs targeting UPR-related components induce cancer cell death and suppress tumor growth. In this review, we comprehensively summarize recent studies on the molecular mechanisms of UPR activation in C. elegans and mammals and elucidate the conceptual framework, functional aspects, and implications of the UPR for cancer therapy. In summary, we paint a developmental landscape of the UPR in different types of cancer and offer valuable insights for the development of novel cancer treatment strategies by targeting the UPR.

摘要

线粒体是重要的细胞器,在能量代谢、细胞凋亡和各种细胞过程中发挥着关键作用。越来越多的证据表明,线粒体也参与了癌症的发生和发展。线粒体未折叠蛋白反应(UPR)是一种复杂的细胞过程,当线粒体的蛋白质折叠能力超负荷时,就会被激活。UPR 的核心机制包括上游调节因子、线粒体伴侣和蛋白酶。这些组件协同工作,以消除错误折叠的蛋白质、增加蛋白质折叠能力并恢复线粒体功能。最近的研究表明,UPR 在各种癌症中失调,促进肿瘤的起始、生长、转移和治疗耐药性。鉴于 UPR 在肿瘤发生中的关键作用,许多针对 UPR 相关成分的化合物和合成药物可诱导癌细胞死亡并抑制肿瘤生长。在这篇综述中,我们全面总结了 UPR 在秀丽隐杆线虫和哺乳动物中激活的分子机制,并阐明了 UPR 对癌症治疗的概念框架、功能方面和意义。总的来说,我们描绘了 UPR 在不同类型癌症中的发展情况,并为通过靶向 UPR 开发新型癌症治疗策略提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ecd/11390889/2288e8a3106e/41419_2024_7049_Fig1_HTML.jpg

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