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

被引:62
|
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
来源
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
相关论文
共 50 条
  • [41] Optimal Evaluation of Programmed Death Ligand-1 on Tumor Cells Versus Immune Cells Requires Different Detection Methods
    Schats, Kelly A.
    Van Vre, Emily A.
    Boeckx, Carolien
    De Bie, Martine
    Schrijvers, Dorien M.
    Neyns, Bart
    De Meester, Ingrid
    Kockx, Mark M.
    ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE, 2018, 142 (08) : 982 - 991
  • [42] Programmed death ligand-1 is associated with tumor infiltrating lymphocytes and poorer survival in urothelial cell carcinoma of the bladder
    Wang, Bo
    Pan, Wenwei
    Yang, Meihua
    Yang, Wenjuan
    He, Wang
    Chen, Xu
    Bi, Junming
    Jiang, Ning
    Huang, Jian
    Lin, Tianxin
    CANCER SCIENCE, 2019, 110 (02) : 489 - 498
  • [43] Expression of programmed death ligand-1 on tumor cells varies pre and post chemotherapy in non-small cell lung cancer
    Jin Sheng
    Wenfeng Fang
    Juan Yu
    Nan Chen
    Jianhua Zhan
    Yuxiang Ma
    Yunpeng Yang
    Yan Huang
    Hongyun Zhao
    Li Zhang
    Scientific Reports, 6
  • [44] Expression of programmed death ligand-1 on tumor cells varies pre and post chemotherapy in non-small cell lung cancer
    Sheng, Jin
    Fang, Wenfeng
    Yu, Juan
    Chen, Nan
    Zhan, Jianhua
    Ma, Yuxiang
    Yang, Yunpeng
    Yanhuang
    Zhao, Hongyun
    Zhang, Li
    SCIENTIFIC REPORTS, 2016, 6
  • [45] Inhibition of Programmed Death Receptor-1/Programmed Death Ligand-1 Interactions by Ginsenoside Metabolites
    Yim, Nam-Hui
    Kim, Young Soo
    Chung, Hwan-Suck
    MOLECULES, 2020, 25 (09):
  • [46] Tumor Progression by Immune Evasion in Melanoma Role of the Programmed Cell Death-1/Programmed Cell Death-1 Ligand 1 Interaction
    Kashani-Sabet, Mohammed
    CANCER, 2010, 116 (07) : 1623 - 1625
  • [47] Structural insights and binding analysis for determining the molecular bases for programmed cell death protein ligand-1 inhibition
    Acurcio, Rita C.
    Leonardo-Sousa, Carlota
    Garcia-Sosa, Alfonso T.
    Salvador, Jorge A.
    Florindo, Helena F.
    Guedes, Rita C.
    MEDCHEMCOMM, 2019, 10 (10) : 1810 - 1818
  • [48] Tumor cell Programmed Death Ligand-1-mediated T cell suppression is overcome by co-expression of CD80
    Haile, Samuel
    Bosch, Jacobus
    Zeender, Annette
    Srivastava, Minu
    Rodel, Sabine
    Wolf, Julie
    Ksander, Bruce
    Ostrand-Rosenberg, Suzanne
    JOURNAL OF IMMUNOLOGY, 2011, 186
  • [49] Programmed Cell Death Ligand-1 (PDL-1) Correlates With Tumor Infiltration by Immune Cells and Represents a Promising Target for Immunotherapy in Endometrial Cancer
    Hecking, Thomas
    Thiesler, Thore
    Halbe, Janina
    Otten, Lucia
    Recker, Florian
    Gevensleben, Heidrun
    Mueller, Tim
    Schiller, Cynthia
    Egger, Eva K.
    Fimmers, Rolf
    Stope, Matthias B.
    Kristiansen, Glen
    Mustea, Alexander
    ANTICANCER RESEARCH, 2022, 42 (03) : 1367 - 1376
  • [50] Interleukin-17A facilitates tumor progression via upregulating programmed death ligand-1 expression in hepatocellular carcinoma
    Yang, Zhong-Xia
    Zhang, Li-Ting
    Liu, Xiao-Jun
    Peng, Xue-Bin
    Mao, Xiao-Rong
    WORLD JOURNAL OF GASTROINTESTINAL ONCOLOGY, 2025, 17 (01)