CD44细胞
癌症干细胞
雷公藤醇
卵巢癌
癌症研究
车站3
下调和上调
CD24型
癌细胞
化学
干细胞
癌症
转移
细胞
生物
医学
细胞凋亡
内科学
细胞生物学
生物化学
基因
作者
Na Li,Chaobo Li,Juan Zhang,Qian Jiang,Zhaoxue Wang,Shao‐Zhen Nie,Zhenzhen Gao,Guangyao Li,Hao Fang,Shaoda Ren,Xiaojing Li
标识
DOI:10.1016/j.cbi.2022.110172
摘要
The hallmark of ovarian cancer is its high mortality rate attributed to the existence of cancer stem cells (CSCs) subpopulations which result in therapy recurrence and metastasis. A series of C-29-substituted and/or different A/B ring of celastrol derivatives were synthesized and displayed potential inhibition against ovarian cancer cells SKOV3, A2780 and OVCAR3. Among them, compound 6c exhibited the most potent anti-proliferative activity and selectivity, gave superior anti-CSC effects through inhibition of the sphere formation and downregulation of the percentage of CD44+CD24− and ALDH+ cells. Further mechanism research demonstrated that compound 6c could attenuate the expression of STAT3 and p-STAT3. The results suggested that the inhibition of celastrol derivative 6c on ovarian cancer cells may be related to resistance to cancer stem-like characters and regulation of STAT3 pathway.
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