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靶向铁死亡途径:癌症治疗的新策略。

Targeting Ferroptosis Pathways: A Novel Strategy for Cancer Therapy.

机构信息

Department of Biotechnology, Atmiya University, Rajkot-360005, India.

出版信息

Curr Cancer Drug Targets. 2022;22(3):234-244. doi: 10.2174/1568009622666220211122745.

Abstract

Ferroptosis is an iron-dependent nonapoptotic kind of regulated cell death resulting from the destruction of redox balance in the cytosol. Unlike apoptosis, ferroptosis is caused by an increase in intracellular iron and lipid peroxides that causes significant damage to the membrane lipid bilayer and mitochondria leading to cell death. Increased iron level in the cell promotes ROS production. Ferroptosis inducer molecules increase ROS production and inhibit the antioxidant defence mechanism to facilitate ferroptosis in cancer cells. Inhibition of GPX4, redox-active iron availability, and lipid peroxidation are major contributors to ferroptosis. Ferroptosis is involved in many diseases like heart disease, neurodegenerative disease, and cancer. Ferroptosis induction recently emerged as an attractive strategy for cancer therapy. In this review, we discuss the regulatory mechanism of ferroptosis, its different hallmarks, including genetic and metabolic regulators and inducers that promote ferroptosis in the cancer cells. Finally, the latest progress and development in ferroptosis research in different cancers focusing on proposing a novel strategy in cancer therapy are discussed.

摘要

铁死亡是一种依赖铁的非细胞凋亡形式的细胞程序性死亡,是由于细胞质中氧化还原平衡的破坏导致的。与细胞凋亡不同,铁死亡是由细胞内铁和脂质过氧化物的增加引起的,这些物质会导致细胞膜脂质双层和线粒体的严重损伤,从而导致细胞死亡。细胞内铁水平的增加会促进 ROS 的产生。铁死亡诱导分子会增加 ROS 的产生并抑制抗氧化防御机制,从而促进癌细胞中的铁死亡。GPX4 的抑制、氧化还原活性铁的可用性和脂质过氧化是铁死亡的主要贡献因素。铁死亡参与了许多疾病,如心脏病、神经退行性疾病和癌症。铁死亡的诱导最近成为癌症治疗的一种有吸引力的策略。在这篇综述中,我们讨论了铁死亡的调节机制,包括遗传和代谢调节剂以及促进癌细胞铁死亡的诱导剂。最后,讨论了不同癌症中铁死亡研究的最新进展和发展,重点提出了一种癌症治疗的新策略。

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