泊马度胺
细胞凋亡
尿素
化学
细胞生长
细胞培养
体外
癌症研究
IC50型
组合化学
程序性细胞死亡
药理学
生物化学
生物
免疫学
多发性骨髓瘤
遗传学
沙利度胺
作者
Yajie Guo,Xi Wang,Zhenzhen Wang,Longfei Mao,Jiahao Wang,Lizeng Peng,Gelin Xu
出处
期刊:Pharmaceuticals
[Multidisciplinary Digital Publishing Institute]
日期:2022-11-27
卷期号:15 (12): 1479-1479
被引量:1
摘要
In order to explore novel immunomodulatory agents as anti-tumor drugs, we designed and synthesized a series of new pomalidomide derivatives containing urea moieties. Interestingly, in vitro biological experiments performed in several cancer cell lines showed that some of them displayed potent anti-tumor ability. These novel compounds 5a–5e and 6a–6e demonstrated the best cell growth inhibitive activity in human breast cancer cell lines MCF-7, but weaker inhibitive activity in human hepatocellular carcinoma cell lines Huh7. Moreover, compound 5d had the most powerful effects in this study, with an IC50 value of 20.2 μM in MCF-7. Further study indicated that compound 5d could inhibit cell growth and induce cell death in a concentration-dependent manner. Besides, compound 5d increased cellular ROS levels and induced DNA damage, thereby potentially leading to cell apoptosis. These observations suggest that the novel pomalidomide derivatives containing urea moieties may be worth further investigation to generate potential anti-tumor drugs.
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