Guo Yajie, Wang Xi, Wang Zhenzhen, Mao Longfei, Wang Jiahao, Peng Lizeng, Xu Guiqing
The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen 518033, China.
School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453007, China.
Pharmaceuticals (Basel). 2022 Nov 27;15(12):1479. doi: 10.3390/ph15121479.
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 - and - 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 had the most powerful effects in this study, with an IC value of 20.2 μM in MCF-7. Further study indicated that compound could inhibit cell growth and induce cell death in a concentration-dependent manner. Besides, compound 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.
为了探索新型免疫调节药物作为抗肿瘤药物,我们设计并合成了一系列含有脲基的新泊马度胺衍生物。有趣的是,在几种癌细胞系中进行的体外生物学实验表明,其中一些表现出强大的抗肿瘤能力。这些新型化合物在人乳腺癌细胞系MCF-7中表现出最佳的细胞生长抑制活性,但在人肝癌细胞系Huh7中的抑制活性较弱。此外,化合物在本研究中具有最强大的作用,在MCF-7中的IC值为20.2μM。进一步的研究表明,化合物可以浓度依赖性方式抑制细胞生长并诱导细胞死亡。此外,化合物增加了细胞内活性氧水平并诱导DNA损伤,从而可能导致细胞凋亡。这些观察结果表明,含有脲基的新型泊马度胺衍生物可能值得进一步研究以开发潜在的抗肿瘤药物。