The State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University, Tianjin, 300071, People's Republic of China.
The State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Nankai University, Tianjin, 300071, People's Republic of China; School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, 300072, People's Republic of China.
Eur J Med Chem. 2018 Aug 5;156:21-42. doi: 10.1016/j.ejmech.2018.06.046. Epub 2018 Jun 20.
Cancer stem cells (CSCs) are responsible for carcinogenesis, cancer progression, relapse, metastasis and drug resistance. Therefore, the development of drug molecules targeting CSCs plays a vital role in medicinal researching field. However, there are extremely rare molecules that selectively ablate CSCs. The research and development of drugs targeting CSCs is limited due to a lack of anti-CSCs lead compounds. In this study, an anti-CSCs lead compound 35b was discovered, which was derived from the natural chemical scaffold of Symplostatin 4. This compound exhibited a significantly suppressive effect on tumor growth both in vitro and in vivo. Additionally, 35b could significantly reduce the number of melanoma tumor spheres and decrease the percentage of ALDH melanoma cells. Further mechanism study illustrated that compound 35b could eliminate the melanoma CSCs by efficiently blocking Wnt/β-catenin signaling pathway. Collectively, our findings would provide a novel chemical scaffold and alternative idea of molecular design for development of anti-CSCs drugs.
癌症干细胞(CSCs)是导致癌症发生、癌症进展、复发、转移和耐药的根源。因此,开发针对 CSCs 的药物分子在医学研究领域中具有至关重要的作用。然而,能够选择性地清除 CSCs 的分子极为罕见。由于缺乏针对 CSCs 的先导化合物,针对 CSCs 的药物研发受到限制。在这项研究中,发现了一种源自 Symplostatin 4 的天然化学支架的抗 CSCs 先导化合物 35b。该化合物在体外和体内均对肿瘤生长具有显著的抑制作用。此外,35b 可显著减少黑色素瘤肿瘤球的数量,并降低 ALDH 黑色素瘤细胞的比例。进一步的机制研究表明,化合物 35b 通过有效阻断 Wnt/β-catenin 信号通路来消除黑色素瘤 CSCs。总之,我们的研究结果为开发抗 CSCs 药物提供了一种新的化学支架和分子设计的替代思路。