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The induction of apoptosis in proliferating human fibroblasts by oxygen radicals is associated with a p53‐ and p21<sup>WAF1CIP1</sup> induction
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Citations
31
References
1997
Year
Lipid PeroxidationApoptosisPathologyCell DeathReactive Oxygen SpeciesCell Death MechanismsRedox BiologyTumor BiologyOxidative StressH IncubationMm HxCancer Cell BiologyCancer ResearchRedox SignalingReactive Oxygen SpecieCell BiologyTumor MicroenvironmentReductive StressTumor SuppressorHuman FibroblastsMedicineOxygen Radicals
The role of reactive oxygen species (ROS) generated by hypoxanthine/xanthine oxidase (HX/XO) in the induction of apoptosis was studied in the human fibroblast cell line WI38. Apoptosis but not necrosis was observed in proliferating fibroblasts after 48 h incubation with 1 mM HX and 0.05 U/ml XO. Induction of apoptosis was hindered by catalase. Cell-cycle analysis revealed a reduction of cells in the S/G2 phase 24 and 48 h after stimulation, suggesting that ROS induce a G1 arrest in proliferating fibroblasts. This was supported by an accumulation of p53 and the cdk inhibitor p21WAF1/CIP1. Since apoptosis was not inducible in senescent fibroblasts our data indicate that ROS mainly induces apoptosis in proliferating cells.
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