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This was emphasised in the CANTOS trial, in which a monoclonal antibody targeting IL-1 in individuals with established atherosclerotic CVD and evidence of systemic inflammation reduced the risk of major adverse cardiovascular events (MACE) by 1517%, an effect that was likely to be mediated by reductions in serum CRP concentrations [80, 81]

In glioblastoma (GBM) patients, oxidative stress leaded to elevated APE1 levels, which increased repair of the AP sites from the chemotherapy, leading to increased drug resistance

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