Arbutin overcomes tumor immune tolerance by inhibiting tumor programmed cell death-ligand 1 expression

被引:0
作者
Liu, Ching-Han
Weng, Jing-Ru [1 ]
Wu, Li-Hsien [1 ,2 ]
Song, Rui-Yang [2 ]
Huang, Ming-Der [2 ]
Wu, Xin-He
Wang, Chia C. [3 ,4 ]
Lee, Che-Hsin [2 ,3 ,5 ,6 ,7 ]
机构
[1] Natl Sun Yat Sen Univ, Dept Marine Biotechnol & Resources, Kaohsiung 80424, Taiwan
[2] Natl SunYat sen Univ, Dept Biol Sci, Kaohsiung, Taiwan
[3] Natl Sun Yat Sen Univ, Aerosol Sci Res Ctr, Kaohsiung, Taiwan
[4] Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan
[5] Natl Sun Yat Sen Univ, Coll Semicond & Adv Technol Res, Kaohsiung 80424, Taiwan
[6] Kaohsiung Med Univ, Dept Med Lab Sci & Biotechnol, Kaohsiung 80708, Taiwan
[7] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
来源
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES | 2024年 / 21卷 / 15期
关键词
Arbutin; programmed cell death protein ligand-1; tumor immune tolerance;
D O I
10.7150/ijms.92419
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:2992 / 3002
页数:11
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