染色质重塑
光亲和标记
癌症研究
生物
结直肠癌
组蛋白
癌症
组蛋白H3
原人参二醇
基因沉默
染色质
化学
代谢物
细胞生物学
生物化学
计算生物学
人参
结合位点
遗传学
医学
DNA
替代医学
人参皂甙
病理
基因
作者
Fang‐Fang Zhuo,Qiang Guo,Yong‐Zhe Zheng,Tingting Liu,Zhuo Yang,Qi‐He Xu,Yong Jiang,Dan Liu,Ke‐Wu Zeng,Pengfei Tu
出处
期刊:ChemBioChem
[Wiley]
日期:2022-04-20
卷期号:23 (13)
被引量:8
标识
DOI:10.1002/cbic.202200038
摘要
Protopanaxadiol (PPD), a main ginseng metabolite, exerts powerful anticancer effects against multiple types of cancer; however, its cellular targets remain elusive. Here, we synthesized a cell-permeable PPD probe via introducing a bifunctional alkyne-containing diazirine photo-crosslinker and performed a photoaffinity labeling-based chemoproteomic study. We identified retinoblastoma binding protein 4 (RBBP4), a chromatin remodeling factor, as an essential cellular target of PPD in HCT116 colorectal cancer cells. PPD significantly decreased RBBP4-dependent trimethylation at lysine 27 of histone H3 (H3K27me3), a crucial epigenetic marker that correlates with histologic signs of colorectal cancer aggressiveness, and PPD inhibition of proliferation and migration of HCT116 cells was antagonized by RBBP4 RNA silencing. Collectively, our study highlights a previously undisclosed anti-colorectal cancer cellular target of the ginseng metabolite and advances the fundamental understanding of RBBP4 functions via a chemical biology strategy.
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