Emerging targets for cancer treatment: S100A9/RAGE

被引:8
|
作者
Valiente, M. [1 ,6 ]
Sepulveda, J. M. [2 ,3 ,7 ]
Perez, A. [2 ,3 ,4 ,5 ,7 ]
机构
[1] CNIO, Brain Metastasis Grp, Madrid, Spain
[2] Hosp Univ 12 Octubre, Neurooncol Unit, Madrid, Spain
[3] Inst Invest Sanitaria Hosp 12 Octubre imas12, Madrid, Spain
[4] Hosp Univ 12 Octubre, Serv Neurocirugia, Madrid, Spain
[5] Univ Complutense Madrid, Fac Med, Dept Cirugia, Madrid, Spain
[6] CNIO, Brain Metastasis Grp, Madrid 28029, Spain
[7] Neurooncol Unit, Ave Cordoba,S-N, Madrid 28041, Spain
关键词
RAGE; NF-KB; JunB; brain metastasis; radioresistance; observational prospective study; clinical trial with RAGE inhibitor; RECEPTOR; RAGE;
D O I
10.1016/j.esmoop.2022.100751
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Developing better treatments that work for the majority of patients with brain metastasis (BM) is highly necessary. Complementarily, avoiding those therapeutic procedures that will not benefit a specific patient is also very relevant. In general, existing therapies for patients with BM could be improved in terms of molecular stratification and therapeutic efficacy. By questioning the benefit of whole brain radiotherapy as provided nowadays and the lack of biomarkers detecting radioresistance, we identified S100A9 and receptor for advanced glycation end-products (RAGE) as a liquid biopsy biomarker and a potential target for a radiosensitizer, respectively. Both of them are being clinically tested as part of the first comprehensive molecular strategy to personalized radiotherapy in BM.
引用
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页数:5
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