British Journal of Cancer · 2010 · 139 citations · 29 references
Life SciencesCancer BiologyOncologyBreast OncologyDna RepairMolecular OncologyAntioxidant DefenseDna Repair In CarcinogenesisOxidative Damage To BiomoleculesOxidative StressOxidative Stress MechanismsReactive Oxygen Species8-Oxo-7, 8-DihydroguanineDna Oxidative AdductsOxidative Damage BiomarkersOxidative Dna DamageOxidative Dna LesionsOxidative Strand BreaksOxidative Stress In CancerPrognostic Biomarkers
BACKGROUND: 8-Hydroxydeoxyguanosine (8-oxodG) is the commonly used marker of oxidative stress-derived DNA damage. 8-OxodG formation is regulated by local antioxidant capacity and DNA repair enzyme activity. Earlier studies have reported contradictory data on the function of 8-oxodG as a prognostic factor in different cancer types. METHODS: We assessed pre-operative serum 8-oxodG levels with an enzyme-linked immunosorbent assay in a well-defined series of 173 breast cancer patients. 8-OxodG expression in the nuclei of cancer cells from 150 of these patients was examined by immunohistochemistry. RESULTS: The serum 8-oxodG levels and immunohistochemical 8-oxodG expression were in concordance with each other (P<0.05). Negative 8-oxodG immunostaining was an independent prognostic factor for poor breast cancer-specific survival according to the multivariate analysis (P<0.01). This observation was even more remarkable when ductal carcinomas only (n=140) were considered (P<0.001). A low serum 8-oxodG level was associated statistically significantly with lymphatic vessel invasion and a positive lymph node status. CONCLUSIONS: Low serum 8-oxodG levels and a low immunohistochemical 8-oxodG expression were associated with an aggressive breast cancer phenotype. In addition, negative 8-oxodG immunostaining was a powerful prognostic factor for breast cancer-specific death in breast carcinoma patients.
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