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厚朴酚通过上调急性髓系白血病细胞中的血红素加氧酶1诱导铁死亡。

Honokiol Induces Ferroptosis by Upregulating HMOX1 in Acute Myeloid Leukemia Cells.

作者信息

Lai Xingrong, Sun Yanhua, Zhang Xuedi, Wang Dan, Wang Jialing, Wang Haihua, Zhao Yao, Liu Xinling, Xu Xin, Song Haoran, Ping Wenjia, Sun Yanli, Hu Zhenbo

机构信息

Laboratory for Stem Cell and Regenerative Medicine, Affiliated Hospital of Weifang Medical University, Weifang, China.

Weifang Medical University, Weifang, China.

出版信息

Front Pharmacol. 2022 May 11;13:897791. doi: 10.3389/fphar.2022.897791. eCollection 2022.

Abstract

Acute myeloid leukemia (AML) is one of the malignant hematological cancers with high mortality. Finding a more effective and readily available treatment is of the utmost importance. Here, we aimed to identify the anti-leukemia effect of a natural small molecule compound honokiol on a panel of AML cell lines, including THP-1, U-937, and SKM-1, and explored honokiol's potential biological pathways and mechanisms. The results showed that honokiol decreased the viability of the targeted AML cells, induced their cell cycle arrest at G0/G1 phase, and inhibited their colony-formation capacity. Honokiol also triggers a noncanonical ferroptosis pathway in THP-1 and U-937 cells by upregulating the level of intracellular lipid peroxide and HMOX1 significantly. Subsequent studies verified that HMOX1 was a critical target in honokiol-induced ferroptosis. These results reveal that honokiol is an effective anti-leukemia agent in AML cell lines and may be a potential ferroptosis activator in AML.

摘要

急性髓系白血病(AML)是死亡率很高的恶性血液癌症之一。找到更有效且易于获得的治疗方法至关重要。在此,我们旨在确定天然小分子化合物厚朴酚对一组AML细胞系(包括THP-1、U-937和SKM-1)的抗白血病作用,并探索厚朴酚潜在的生物学途径和机制。结果表明,厚朴酚降低了靶向AML细胞的活力,诱导其细胞周期停滞于G0/G1期,并抑制其集落形成能力。厚朴酚还通过显著上调细胞内脂质过氧化物和HMOX1的水平,在THP-1和U-937细胞中触发非经典铁死亡途径。后续研究证实,HMOX1是厚朴酚诱导铁死亡的关键靶点。这些结果表明,厚朴酚是AML细胞系中一种有效的抗白血病药物,可能是AML中潜在的铁死亡激活剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cbe/9132251/342808b36986/fphar-13-897791-g001.jpg

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