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白花丹醌靶向硫氧还蛋白还原酶有助于诱导HL-60细胞凋亡。

Targeting thioredoxin reductase by plumbagin contributes to inducing apoptosis of HL-60 cells.

作者信息

Zhang Junmin, Peng Shoujiao, Li Xinming, Liu Ruijuan, Han Xiao, Fang Jianguo

机构信息

State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, Gansu 730000, China; School of Pharmacy, Lanzhou University, Lanzhou, Gansu 730000, China.

State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, Gansu 730000, China.

出版信息

Arch Biochem Biophys. 2017 Apr 1;619:16-26. doi: 10.1016/j.abb.2017.02.007. Epub 2017 Feb 27.

Abstract

Plumbagin (PLB), a natural naphthoquinone from the traditional folk medicines Plumbago zeylanica, Dionaea muscipula, or Nepenthes gracilis, has been documented possessing a wide variety of pharmacological activities. Although PLB demonstrates anticancer activity in multiple types of malignant cells, the cellular targets of PLB have not been well defined and remained only partially understood. We reported here that PLB selectively inhibits TrxR and elicits reactive oxygen species in human promyelocytic leukemia HL-60 cells, which leads to elevation of GSSG/GSH ratio and decrease of cellular thiol pool. As a consequence, PLB disturbs the cellular redox homeostasis, induces oxidative stress-mediated apoptosis and eventually selectively kills HL-60 cells. Inhibition of TrxR by PLB thus discloses an unprecedented mechanism underlying the anticancer efficacy of PLB, and sheds light in considering the usage of PLB as a promising cancer therapeutic agent.

摘要

白花丹素(PLB)是一种从传统民间药物白花丹、捕蝇草或细叶猪笼草中提取的天然萘醌,已被证明具有多种药理活性。尽管PLB在多种恶性细胞中表现出抗癌活性,但其细胞靶点尚未明确界定,仍仅得到部分了解。我们在此报告,PLB在人早幼粒细胞白血病HL-60细胞中选择性抑制硫氧还蛋白还原酶(TrxR)并引发活性氧,这导致氧化型谷胱甘肽/还原型谷胱甘肽(GSSG/GSH)比值升高和细胞巯基池减少。因此,PLB扰乱细胞氧化还原稳态,诱导氧化应激介导的细胞凋亡,并最终选择性杀死HL-60细胞。PLB对TrxR的抑制作用揭示了PLB抗癌功效背后前所未有的机制,并为将PLB用作有前景的癌症治疗药物提供了思路。

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