The extracts of Astragalus membranaceus overcome tumor immune tolerance by inhibition of tumor programmed cell death protein ligand-1 expression

被引:64
作者
Chang, Hsu-Liang [1 ]
Kuo, Yi-Hsuan [2 ]
Wu, Li-Hsien [2 ]
Chang, Chih-Min [2 ,3 ]
Cheng, Kai-Jen [2 ,4 ]
Tyan, Yu-Chang [5 ]
Lee, Che-Hsin [2 ,6 ,7 ,8 ,9 ]
机构
[1] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Kaohsiung Municipal Ta Tung Hosp, Dept Internal Med, Kaohsiung 80145, Taiwan
[2] Natl Sun Yat Sen Univ, Dept Biol Sci, 70 Lienhai Rd, Kaohsiung 80424, Taiwan
[3] Chang Gung Mem Hosp, Dept Internal Med, Div Metab, Kaohsiung 833, Taiwan
[4] Kaohsiung Municipal United Hosp, Dept Internal Med, Div Nephrol, Kaohsiung 80457, Taiwan
[5] Kaohsiung Med Univ, Dept Med Imaging & Radiol Sci, Kaohsiung 80145, Taiwan
[6] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung 40402, Taiwan
[7] Kaohsiung Med Univ, Dept Med Lab Sci & Biotechnol, Kaohsiung 804, Taiwan
[8] Natl Sun Yat Sen Univ, Doctoral Degree Program Marine Biotechnol, Kaohsiung 80424, Taiwan
[9] Natl Sun Yat Sen Univ, Aerosol Sci Res Ctr, Kaohsiung 80424, Taiwan
关键词
the extracts of Astragalus membranaceus (PG2); programmed cell death protein ligand-1; tumor immune tolerance;
D O I
10.7150/ijms.42978
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A polysaccharide isolated from the radix of Astragalus membranaceus, called PG2, used in traditional Chinese medicine, with potential hematopoiesis inducing and immunomodulation activities. PG2 extracted from A. membranaceus has been demonstrated as a novel alternative medicine for cancer patients. Recently, we demonstrated that PG2 enhanced chemotherapy through bystander effect and reduced the expression of indoleamine 2, 3-dioxygenase 1 in tumor cells. Many tumors have been proven to have a high expression of programmed cell death protein ligand-1 (PD-L1), which binds with programmed cell death protein-1(PD-1) in immune cells, thus causing immune tolerance within the tumor microenvironment. With decreased expression of PD-L1, increased immune response can be observed, which might be helpful when developing tumor immunotherapy. The antitumor therapeutic effect mediated by PG2 may associate with an inflammatory immune response at the tumor site. However, the molecular mechanism that by which PG2 inhibits PD-L1 is still incompletely known. The expression of PD-L1 was decreased after tumor cells were treated with PG2. In addition, the cell signaling pathway in tumor cells was evaluated by Western blotting analysis after PG2 treatment. PG2 can downregulate the expression of PD-L1 on the cell surface via the protein kinase B (Akt)/mammalian target of rapamycin (mTOR)/ribosomal protein S6 kinase beta-1 (p70S6K) pathway. In conclusion, our results indicate that PG2 inhibits PD-L1 expression and plays a crucial role in immunotherapy, which might be a promising strategy combined with other treatments.
引用
收藏
页码:939 / 945
页数:7
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