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Synthesis and discovery of 18β-glycyrrhetinic acid derivatives inhibiting cancer stem cell properties in ovarian cancer cells

机译:18β-甘草次酸衍生物抑制卵巢癌细胞癌干细胞特性的合成及发现

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Despite advances in ovarian cancer treatment, the five-year overall survival rate is less than 30% with the presence of cancer stem cells (CSCs). To develop CSC-targeting therapy, a series of 18β-glycyrrhetinic acid (GA) derivatives containing cinnamamide moiety have been designed, synthesized, and screened for their antiproliferative activity in SKOV3 and OVCAR3 cells. Most of the compounds exhibited stronger antiproliferative activity than GA, and compound 7c was the most active one. Further biological studies showed that compound 7c could induce apoptosis and suppress migration. In addition, compound 7c could not only observably decrease the colony formation and sphere formation ability, but also significantly reduce the CD44 ~(+) , CD133 ~(+) , and ALDH ~(+) subpopulation in SKOV3 and OVCAR3 cells. In conclusion, these results indicate that compound 7c is a promising anti-CSC agent for further anti-ovarian cancer studies.
机译:尽管卵巢癌治疗取得了进展,但在存在癌症干细胞(CSC)的情况下,五年总生存率仍不到30%。为了开发靶向CSC的疗法,已设计,合成了一系列含有肉桂酰胺部分的18β-甘草次酸(GA)衍生物,并筛选了它们在SKOV3和OVCAR3细胞中的抗增殖活性。大多数化合物显示出比GA更强的抗增殖活性,化合物7c是活性最高的一种。进一步的生物学研究表明,化合物7c可以诱导细胞凋亡并抑制迁移。另外,化合物7c不仅可观察到降低集落形成和球形成能力,而且还显着降低SKOV3和OVCAR3细胞中的CD44〜(+),CD133〜(+)和ALDH〜(+)亚群。总之,这些结果表明,化合物7c是用于进一步抗卵巢癌研究的有希望的抗CSC药物。

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