Department of Integrative Cancer Therapy and Urology, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa, Ishikawa, 920-8640, Japan.
Department of Histology and Cell Biology, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan.
Sci Rep. 2021 Jan 12;11(1):675. doi: 10.1038/s41598-020-80302-4.
Despite improvements in systemic therapy options for renal cancer, it remains one of the most drug-resistant malignancies. Interestingly, reports have shown that kahweol and cafestol, natural diterpenes extracted from coffee beans, exhibit anti-cancer activity. However, the multiple potential pharmacological actions of both have yet to be fully understood. This study therefore investigated the effects of kahweol acetate and cafestol on human renal cancer ACHN and Caki-1 cells. Accordingly, the combination of kahweol acetate and cafestol administration synergistically inhibited cell proliferation and migration by inducing apoptosis and inhibiting epithelial-mesenchymal transition. Mechanistic dissection revealed that kahweol acetate and cafestol inhibited Akt and ERK phosphorylation. Moreover, kahweol acetate and cafestol downregulated the expression of not only C-C chemokine receptors 2, 5, and 6 but also programmed death-ligand 1, indicating their effects on the tumor microenvironment. Thus, kahweol acetate and cafestol may be novel therapeutic candidates for renal cancer considering that they exert multiple pharmacological effects.
尽管肾癌的系统治疗选择有所改善,但它仍然是最具耐药性的恶性肿瘤之一。有趣的是,有报道称,从咖啡豆中提取的天然二萜咖啡醇和咖啡醇具有抗癌活性。然而,这两种物质的多种潜在药理作用尚未被完全理解。因此,本研究探讨了咖啡醇乙酸酯和咖啡醇对人肾癌细胞 ACHN 和 Caki-1 的影响。因此,咖啡醇乙酸酯和咖啡醇联合给药通过诱导细胞凋亡和抑制上皮-间充质转化,协同抑制细胞增殖和迁移。机制分析表明,咖啡醇乙酸酯和咖啡醇抑制 Akt 和 ERK 磷酸化。此外,咖啡醇乙酸酯和咖啡醇不仅下调了 C-C 趋化因子受体 2、5 和 6 的表达,还下调了程序性死亡配体 1 的表达,表明它们对肿瘤微环境的影响。因此,鉴于咖啡醇乙酸酯和咖啡醇具有多种药理作用,它们可能成为治疗肾癌的新候选药物。