4.8 Article

Stratification of radiosensitive brain metastases based on an actionable S100A9/RAGE resistance mechanism

期刊

NATURE MEDICINE
卷 28, 期 4, 页码 752-+

出版社

NATURE PORTFOLIO
DOI: 10.1038/s41591-022-01749-8

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资金

  1. Pla Director d'Oncologia de Catalunya
  2. MINECO [SAF2017-89643-R]
  3. Fundacio La Marato de TV3 [201906-30-31-32]
  4. Fundacion Ramon Areces [CIVP19S8163, CIVP20S10662]
  5. Worldwide Cancer Research [19-0177]
  6. Cancer Research Institute (Clinic and Laboratory Integration Program CRI Award 2018) [54545]
  7. AECC (Coordinated Translational Groups 2017) [GCTRA16015SEOA]
  8. LAB AECC 2019 [LABAE19002VALI]
  9. ERC CoG [864759]
  10. Portuguese Foundation for Science and Technology [SFRH/bd/100089/2014]
  11. Boehringer-Ingelheim Fonds MD Fellowship
  12. La Caixa International PhD Program Fellowship-Marie Skodowska-Curie [LCF/BQ/DI17/11620028]
  13. La Caixa INPhINIT Fellowship [LCF/BQ/DI19/11730044]
  14. MINECO-Severo Ochoa PhD Fellowship [BES-2017-081995]
  15. AECC postdoctoral fellowship [POSTD19016PRIE]
  16. Gertrud and Erich Roggenbuck Stiftung
  17. Science Foundation Ireland [19/FFP/6443, 18/SPP/3522, 20/FFP-P/8597]
  18. Breast Cancer Now [2019AugSF1310]
  19. Paradifference Foundation
  20. la Caixa Foundation [100010434]
  21. European Union's Horizon 2020 research and innovation programme under Marie Skodowska-Curie grant [847648 (CF/BQ/PI20/11760029)]
  22. Champalimaud Centre for the Unknown
  23. Lisboa Regional Operational Programme (Lisboa 2020) [LISBOA01-0145-FEDER-022170]
  24. NCI [R01 CA227629, R01 CA218133]
  25. Fundacio Roses Contra el Cancer
  26. Ministerio de Universidades FPU Fellowship [FPU 18/00069]
  27. MICIN-Agencia Estatal de Investigacion Fellowships [PRE2020-093032, BES-2017-080415]
  28. Ministerio de Ciencia, Innovacion y Universidades [E050251, PID2019-110292RB-I00]
  29. FCT [PTDC/MED-ONC/32222/2017]
  30. Fundacao Millennium bcp
  31. Foundation for Applied Cancer Research in Zurich
  32. Fundação para a Ciência e a Tecnologia [PTDC/MED-ONC/32222/2017, SFRH/BD/100089/2014] Funding Source: FCT
  33. European Research Council (ERC) [864759] Funding Source: European Research Council (ERC)

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This study identifies a molecular mechanism underlying resistance to whole-brain radiotherapy and suggests potential targets and biomarkers for personalized radiotherapy. The findings have important implications for improving the efficacy of treatment for patients with brain metastasis.
A comprehensive analysis of models of brain metastasis and multiple cohorts of patient samples identifies a targetable molecular mechanism underlying the resistance to whole-brain radiotherapy that can inform patient selection for personalized radiotherapy. Whole-brain radiotherapy (WBRT) is the treatment backbone for many patients with brain metastasis; however, its efficacy in preventing disease progression and the associated toxicity have questioned the clinical impact of this approach and emphasized the need for alternative treatments. Given the limited therapeutic options available for these patients and the poor understanding of the molecular mechanisms underlying the resistance of metastatic lesions to WBRT, we sought to uncover actionable targets and biomarkers that could help to refine patient selection. Through an unbiased analysis of experimental in vivo models of brain metastasis resistant to WBRT, we identified activation of the S100A9-RAGE-NF-kappa B-JunB pathway in brain metastases as a potential mediator of resistance in this organ. Targeting this pathway genetically or pharmacologically was sufficient to revert the WBRT resistance and increase therapeutic benefits in vivo at lower doses of radiation. In patients with primary melanoma, lung or breast adenocarcinoma developing brain metastasis, endogenous S100A9 levels in brain lesions correlated with clinical response to WBRT and underscored the potential of S100A9 levels in the blood as a noninvasive biomarker. Collectively, we provide a molecular framework to personalize WBRT and improve its efficacy through combination with a radiosensitizer that balances therapeutic benefit and toxicity.

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