A novel Anti-Cancer Stem Cells compound optimized from the natural symplostatin 4 scaffold inhibits Wnt/β-catenin signaling pathway

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...

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Veröffentlicht in:European journal of medicinal chemistry 2018-08, Vol.156, p.21-42
Hauptverfasser: Liu, Shuangwei, Gao, Xian, Zhang, Lisong, Qin, Shuanglin, Wei, Mingming, Liu, Ning, Zhao, Rui, Li, Benlong, Meng, Ye, Lin, Gang, Lu, Cheng, Liu, Xinhua, Xie, Maodun, Liu, Tongtong, Zhou, Honggang, Qi, Min, Yang, Guang, Yang, Cheng
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Sprache:eng
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Zusammenfassung: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. [Display omitted] •Cancer Stem Cells.•Total Synthesis.•Symplostatin 4.•Depsipeptides.
ISSN:0223-5234
1768-3254
DOI:10.1016/j.ejmech.2018.06.046