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铁死亡在耐药性癌症治疗中的新兴机制和应用。

Emerging mechanisms and applications of ferroptosis in the treatment of resistant cancers.

机构信息

Department of General Surgery, the Fourth Affiliated Hospital of China Medical University, Shenyang, 110032, Liaoning, China.

Department of General Surgery, the Fourth Affiliated Hospital of China Medical University, Shenyang, 110032, Liaoning, China.

出版信息

Biomed Pharmacother. 2020 Oct;130:110710. doi: 10.1016/j.biopha.2020.110710. Epub 2020 Sep 17.

Abstract

The development of chemotherapy drugs has promoted anticancer treatment, but the effect on tumours is not clear because of treatment resistance; thus, it is necessary to further understand the mechanism of cell death to explore new therapeutic targets. As a new type of programmed cell death, ferroptosis is increasingly being targeted in the treatment of many cancers with clinical drugs and experimental compounds. Ferroptosis is stimulated in tumours with inherently high levels of ferrous ions by a reaction with abundant polyunsaturated fatty acids and the inhibition of antioxidant enzymes, which can overcome treatment resistance in cancers mainly through GPX4. In this review, we focus on the intrinsic cellular regulators against ferroptosis in cancer resistance, such as GPX4, NRF2 and the thioredoxin system. We summarize the application of novel compounds and drugs to circumvent treatment resistance. We also introduce the application of nanoparticles for the treatment of resistant cancers. In conclusion, targeting ferroptosis represents a considerable strategy for resistant cancer treatment.

摘要

化疗药物的发展促进了抗癌治疗,但由于治疗耐药性,其对肿瘤的作用尚不清楚;因此,有必要进一步了解细胞死亡的机制,以探索新的治疗靶点。铁死亡作为一种新型的程序性细胞死亡,其在许多癌症的治疗中受到临床药物和实验化合物的靶向作用。在肿瘤中,由于与大量多不饱和脂肪酸的反应和抗氧化酶的抑制,铁离子水平固有较高,从而刺激铁死亡,这可以主要通过 GPX4 来克服癌症的治疗耐药性。在这篇综述中,我们专注于针对癌症耐药性中的铁死亡的内在细胞调节剂,如 GPX4、NRF2 和硫氧还蛋白系统。我们总结了新型化合物和药物在规避治疗耐药性方面的应用。我们还介绍了纳米颗粒在治疗耐药性癌症中的应用。总之,靶向铁死亡是治疗耐药性癌症的一种重要策略。

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