Liu Ching-Han, Weng Jing-Ru, Wu Li-Hsien, Song Rui-Yang, Huang Ming-Der, Wu Xin-He, Wang Chia C, Lee Che-Hsin
Division of Cardiology, Department of Internal Medicine, Kaohsiung Armed Forces General Hospital, Kaohsiung, Taiwan.
Department of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.
Int J Med Sci. 2024 Nov 11;21(15):2992-3002. doi: 10.7150/ijms.92419. eCollection 2024.
Arbutin, predominantly derived from the bearberry plant, exhibits promising immunomodulatory properties. Given its ability to influence the programmed cell death-ligand 1/ programmed cell death-1 (PD-L1/PD-1) pathway, it is emerging as a potential alternative treatment for cancer. A reduced expression of PD-L1, as seen after arbutin treatment, can bolster immune responses critical step in effective tumor immunotherapy. However, the molecular mechanism by which arbutin inhibits PD-L1 is still incompletely known. The expression of PD-L1 was decreased after tumor cells were treated with arbutin. Arbutin can downregulate the expression of PD-L1 on the cell surface via the protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway. The findings suggest the protective role of arbutin and provide novel insights into immunotherapy, which involves inhibiting the AKT/mTOR signaling pathway. Arbutin might serve as a potential therapeutic agent alone or in combination with other treatments.
熊果苷主要来源于熊果植物,具有良好的免疫调节特性。鉴于其能够影响程序性细胞死亡配体1/程序性细胞死亡蛋白1(PD-L1/PD-1)通路,它正成为一种潜在的癌症替代治疗方法。熊果苷治疗后观察到的PD-L1表达降低,可以增强有效肿瘤免疫治疗中的关键免疫反应步骤。然而,熊果苷抑制PD-L1的分子机制仍不完全清楚。肿瘤细胞用熊果苷处理后,PD-L1的表达降低。熊果苷可通过蛋白激酶B(AKT)/雷帕霉素哺乳动物靶蛋白(mTOR)通路下调细胞表面PD-L1的表达。这些发现表明了熊果苷的保护作用,并为免疫治疗提供了新的见解,即抑制AKT/mTOR信号通路。熊果苷可能单独或与其他治疗联合作为一种潜在的治疗药物。