Regulation of PD-L1 expression in K-ras-driven cancers through ROS-mediated FGFR1 signaling.

Glorieux, Christophe;Xia, Xiaojun;He, Yong-Qiao;Hu, Yumin;Huang, Peng;et.al.
(2021) Redox Biology — Vol. 38, p. 101780 [1-12] (2021)

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Authors
  • Glorieux, Christophe
    Author
  • Xia, Xiaojun
    Author
  • He, Yong-Qiao
    Author
  • Hu, Yumin
    Author
  • Crémer, Kellyorcid-logoUCLouvain
    Author
  • Robert, AnnieUCLouvain
    Author
  • Huang, Peng
    Author
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Abstract
K-ras mutations are major genetic events that drive cancer development associated with aggressive malignant phenotypes, while expression of the immune checkpoint molecule PD-L1 plays a key role in cancer evasion of the immune surveillance that also profoundly affects the patient outcome. However, the relationship between K-ras oncogenic signal and PD-L1 expressions as an important area that requires further investigation. Using both in vitro and in vivo experimental models of K-ras-driven cancer, we found that oncogenic K-ras significantly enhanced PD-L1 expression through a redox-mediated mechanism. Activation of K-ras promoted ROS generation and induced FGFR1 expression, leading to a significant upregulation of PD-L1. We further showed that exogenous ROS such as hydrogen peroxide alone was sufficient to activate FGFR1 and induce PD-L1, while antioxidants could largely abrogate PD-L1 expression in K-ras mutant cells, indicating a critical role of redox regulation. Importantly, genetic knockout of FGFR1 led to a decrease in PD-L1 expression, and impaired tumor growth in vivo due to a significant increase of T cell infiltration in the tumor tissues and thus enhanced T-cell-mediated tumor suppression. Our study has identified a novel mechanism by which K-ras promotes PD-L1 expression, and suggests that modulation of ROS or inhibition of the FGFR1 pathway could be a novel strategy to abrogate PD-L1-mediated immunosuppression and thus potentially improve the efficacy of immunotherapy in K-ras-driven cancers.
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Citations

Glorieux, C., Xia, X., He, Y.-Q., Hu, Y., Crémer, K., Robert, A., Liu, J., Wang, F., Ling, J., Chiao, P. J., & Huang, P. (2021). Regulation of PD-L1 expression in K-ras-driven cancers through ROS-mediated FGFR1 signaling. Redox Biology, 38, 101780 [1-12]. https://doi.org/10.1016/j.redox.2020.101780 (Original work published 2021)