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dc.contributor.authorVera Ramírez, Laura 
dc.contributor.authorSanchez-Rovira, Pedro
dc.contributor.authorRamírez Tortosa, María Carmen 
dc.contributor.authorRamírez Tortosa, César Luis 
dc.contributor.authorGranados Principal, Sergio 
dc.contributor.authorLorente Acosta, José Antonio 
dc.contributor.authorQuiles Morales, José Luis 
dc.date.accessioned2025-01-30T09:23:04Z
dc.date.available2025-01-30T09:23:04Z
dc.date.issued2012
dc.identifier.urihttps://hdl.handle.net/10481/101133
dc.description.abstractAntineoplastic agents are known to induce the production of free radicals leading to cell damage. These adverse effects may fuel the acquisition of new mutations and the development of treatment resistances. We selected 30 metastatic breast cancer patients receiving palliative chemotherapy, and paired blood samples, before and after chemotherapy, were extracted. We analysed DNA, lipid and protein oxidative damage markers and determined the extent of antioxidant and repair defences activation at the systemic level. We found that the DNA repair activity of the KU86 enzyme was significantly lower after chemotherapy and the antioxidant capacity of the plasma was significantly higher after treatment. Cox regression analysis revealed a significant effect of KU86 activity on the survival rates of those patients who received anthracyclines as part of their treatment. The high clinical heterogeneity of metastatic breast cancer patients warrants further studies to clarify the role of DNA repair and systemic antioxidant capacities during chemotherapy.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleOxidative stress status in metastatic breast cancer patients receiving palliative 1 chemotherapy and its impact on survival rateses_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3109/10715762.2011.635658
dc.type.hasVersionAMes_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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