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The crosstalk between autophagy and myeloid-derived suppressor cell responses in cancer

  • Jia Nie [1] ; Di Wang [1] ; MingJian Li [1]
    1. [1] Chengdu University of Traditional Chinese Medicine

      Chengdu University of Traditional Chinese Medicine

      China

  • Localización: Clinical & translational oncology, ISSN 1699-048X, Vol. 25, Nº. 10 (October), 2023, págs. 2832-2840
  • Idioma: inglés
  • Texto completo no disponible (Saber más ...)
  • Resumen
    • The development of cancers is aided by the accumulation of myeloid-derived suppressor cells (MDSCs) within tumors, which are highly effective at suppressing anti-tumor immune responses. Direct cell-to-cell interaction and the production of immunosuppressive mediators have both been proposed as pathways for MDSC-mediated suppression of anti-tumor immune responses. The majority of current cancer treatments focus on altering the development and activity of MDSCs so that they have more of an immunogenic character. Autophagy is a catabolic system that contributes to the breakdown of damaged intracellular material and the recycling of metabolites. However, depending on the stage of tumor growth, autophagy can play both a prophylactic and a therapeutic function in carcinogenesis. However, several indirect lines of research have indicated that autophagy is a significant regulator of MDSC activity. The purpose of this work was to outline the interactions between MDSC and autophagy in cancer.


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