4.7 Review

Tumor-intrinsic determinants of immunogenic cell death modalities

Journal

ONCOIMMUNOLOGY
Volume 10, Issue 1, Pages -

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/2162402X.2021.1893466

Keywords

Regulated cell death; immunogenic cell death; cancer immunosurveillance; oncogene; tumor suppressor

Funding

  1. University of Guelph Startup
  2. OICR
  3. Wolf Lebovic Cancer Genomics and Immunity Program
  4. Ligue contre le Cancer (equipe labellisee)
  5. Agence National de la Recherche (ANR)-Projets blancs
  6. ANR
  7. ERA-Net for Research on Rare Diseases [AMMICa US23/CNRS UMS3655]
  8. Association pour la recherche sur le cancer (ARC)
  9. Association Ruban Rose
  10. Canceropole Ile-deFrance
  11. Fondation pour la Recherche Medicale (FRM)
  12. European Research Area Network on Cardiovascular Diseases
  13. Gustave Roussy Odyssea
  14. European Union
  15. Fondation Carrefour
  16. Highend Foreign Expert Program in China [GDW20171100085]
  17. Institut National du Cancer (INCa)
  18. Inserm (HTE)
  19. Institut Universitaire de France
  20. LeDucq Foundation
  21. LabEx Immuno-Oncology [ANR-18-IDEX-0001]
  22. RHU Torino Lumiere
  23. Seerave Foundation
  24. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  25. SIRIC Cancer Research and Personalized Medicine (CARPEM)

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The immune system recognizes tumor cells and initiates a specific T cell response, but tumors have developed mechanisms to evade immune surveillance by suppressing immunogenic cell death.
The immune system can recognize tumor cells to mount antigen-specific T cell response. Central to the establishment of T cell-mediated adaptive immunity are the inflammatory events that facilitate antigen presentation by stimulating the expression of MHC and costimulatory molecules and the secretion of pro-inflammatory cytokines. Such inflammatory events can be triggered upon cytotoxic treatments that induce immunogenic cancer cell death modalities. However, cancers have acquired a plethora of mechanisms to subvert, or to hide from, host-encoded immunosurveillance. Here, we discuss how tumor intrinsic oncogenic factors subvert desirable intratumoral inflammation by suppressing immunogenic cell death.

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