转录因子HBP1通过调节UHRF1-CDO1轴来促进瘤细胞中的铁亡
Ruixiang Yang1, Yue Zhou1, Tongjia Zhang1
1Department of Biochemistry and Biophysics, School of Basic Medical Sciences, Beijing Key Laboratory of Protein Posttranslational Modifications and Cell Function, Peking University Health Science Center, Beijing, China.
PLoS biology
|July 5, 2023
概括
转录因子HBP1通过对UHRF1进行下调和对CDO1.1进行上调来促进瘤细胞中的铁亡. 覆盖金属聚烯网络的HBP1纳米颗粒通过准HBP1-UHRF1-CDO1轴,有效地抑制瘤生长.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 纳米技术纳米技术
背景情况:
- 诱导铁亡是抑制瘤进展的关键策略,但其调节机制尚未完全理解.
- 转录因子HBP1在瘤细胞抗氧化能力和铁亡中的作用需要进一步研究.
研究的目的:
- 阐明HBP1在调节瘤细胞铁亡中的新功能.
- 探索基于HBP1的纳米颗粒在癌症治疗中的治疗潜力.
主要方法:
- 研究了HBP1在转录水平上对UHRF1基因表达的调节.
- 研究了通过降低UHRF1水平来调节CDO1的表观遗传学.
- 为瘤细胞向和诱导铁亡,制造并测试了金属多网络涂层的HBP1纳米粒子 (MPN-HBP1).
主要成果:
- 通过抑制其基因表达,HBP1降低了UHRF1蛋白水平.
- 减少的UHRF1在表观遗传上调节CDO1,增强癌细胞中铁灭的敏感性.
- 通过调节HBP1-UHRF1-CDO1轴,MPN-HBP1纳米颗粒有效诱导铁和抑制瘤增殖.
结论:
- 通过HBP1-UHRF1-CDO1通路,HBP1在调节铁中发挥着至关重要的作用.
- 通过诱导铁亡,MPN-HBP1纳米颗粒代表了癌症治疗的有前途的纳米药物.
- 这项研究为ferroptosis调节及其在瘤学中的治疗应用提供了新的见解.
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