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  • [Oncotarget.] The TLR7 agonist imiquimod induces anti-cancer effects via autophagic cell death and enhances anti-tumoral and systemic immunity during radiotherapy for melanoma.

    강원대/ 정유진*

  • 출처
    Oncotarget.
  • 등재일
    2017 Feb 15
  • 저널이슈번호
    doi: 10.18632/oncotarget.15326. [Epub ahead of print]
  • 내용

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    Abstract

    Toll-like receptor (TLR) ligands are strongly considered immune-adjuvants for cancer immunotherapy and have been shown to exert direct anti-cancer effects. This study was performed to evaluate the synergistic anti-cancer and anti-metastatic effects of the TLR7 agonist imiquimod (IMQ) during radiotherapy for melanoma. The pretreatment of B16F10 or B16F1 cells with IMQ combined with γ-ionizing radiation (IR) led to enhanced cell death via autophagy, as demonstrated by increased expression levels of autophagy-related genes, and an increased number of autophagosomes in both cell lines. The results also confirmed that the autophagy process was accelerated via the reactive oxygen species (ROS)-mediated MAPK and NF-κB signaling pathway in the cells pretreated with IMQ combined with IR. Mice subcutaneously injected with melanoma cells showed a reduced tumor growth rate after treatment with IMQ and IR. Treatment with 3-methyladenine (3-MA), ameliorated the anti-cancer effect of IMQ combined with IR. Additionally, the combination therapy enhanced anti-cancer immunity, as demonstrated by an increased number of CD8+ T cells and decreased numbers of regulatory T cells (Treg) and myeloid-derived suppressor cells (MDSCs) in the tumor lesions. Moreover, the combination therapy decreased the number of metastatic nodules in the lungs of mice that were injected with B16F10 cells via the tail vein. In addition, the combination therapy enhanced systemic anti-cancer immunity by increasing the abundances of T cell populations expressing IFN-γ and TNF-α. Therefore, these findings suggest that IMQ could serve as a radiosensitizer and immune booster during radiotherapy for melanoma patients. 

     

    Author information

    Cho JH1, Lee HJ1, Ko HJ2, Yoon BI3, Choe J4, Kim KC1, Hahn TW3, Han JA5, Choi SS6, Jung YM7, Lee KH8, Lee YS9, Jung YJ1.

    1Department of Biological Sciences, Kangwon National University, Chuncheon, Republic of Korea.

    2College of Pharmacy, Kangwon National University, Chuncheon, Republic of Korea.

    3Department of Veterinary Medicine, Kangwon National University, Chuncheon, Republic of Korea.

    4Department of Microbiology, School of Medicine, Kangwon National University, Chuncheon, Republic of Korea.

    5Department of Biochemistry and Molecular Biology, School of Medicine, Kangwon National University, Chuncheon, Republic of Korea.

    6Department of Medical Biotechnology, College of Biomedical Science, Kangwon National University, Chuncheon, Republic of Korea.

    7Department of Chemistry, Kangwon National University, Chuncheon, Republic of Korea.

    8Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences, Nowon-gu, Seoul, Republic of Korea.

    9Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seodaemun-gu, Seoul, Republic of Korea. 

  • 키워드
    TLR7; autophagy; imiquimod (IMQ); melanoma; radiotherapy
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