Publication | Closed Access
Potentiation of irinotecan sensitivity by Se-methylselenocysteine in an in vivo tumor model is associated with downregulation of cyclooxygenase-2, inducible nitric oxide synthase, and hypoxia-inducible factor 1α expression, resulting in reduced angiogenesis
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Citations
42
References
2006
Year
Redox SignalingTumor BiologyAngiogenesisIrinotecan SensitivityRedox RegulatorMedicineVivo Tumor ModelHypoxia-inducible Factor 1αCancer Cell BiologyVascular BiologyReactive Oxygen SpeciePharmacologyCell BiologyRedox BiologyCancer ResearchOxidative Stress
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