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• W3215865552 endingPage "1925" @default.
• W3215865552 startingPage "1925" @default.
• W3215865552 abstract "Prostate cancer occurs frequently in men and can often lead to death. Many cancers, including prostate cancer, can be initiated by oxidative insult caused by free radicals and reactive oxygen species. The superoxide dismutase family removes the oxygen-derived reactive oxygen species, and increased superoxide dismutase activity can often be protective against prostate cancer. Prostate cancer can be treated in a variety of ways, including surgery, androgen deprivation therapy, radiation therapy, and chemotherapy. The clinical trajectory of prostate cancer varies from patient to patient, but more aggressive tumors often tend to be radioresistant. This is often due to the free-radical and reactive-oxygen-species-neutralizing effects of the superoxide dismutase family. Superoxide dismutase 2, which is especially important in this regard, can be induced by the NF-κB pathway, which is an important mechanism in radioresistance. This information has enabled the development of interventions that manipulate the NF-κB mechanism to treat prostate cancer." @default.
• W3215865552 created "2021-12-06" @default.
• W3215865552 creator A5019750519 @default.
• W3215865552 creator A5039300756 @default.
• W3215865552 date "2021-11-30" @default.
• W3215865552 modified "2023-10-18" @default.
• W3215865552 title "Radioresistance in Prostate Cancer: Focus on the Interplay between NF-κB and SOD" @default.
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• W3215865552 doi "https://doi.org/10.3390/antiox10121925" @default.
• W3215865552 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34943029" @default.
• W3215865552 hasPublicationYear "2021" @default.
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