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- W2059852859 endingPage "192" @default.
- W2059852859 startingPage "186" @default.
- W2059852859 abstract "Prostate cancer is the most common non-cutaneous cancer in Western males. The majority of prostate cancer fatalities are caused by development of castration-resistant growth and metastatic spread of the primary tumor. The average duration of the response of primary prostate cancer to hormonal ablation is less than 3 years, and 75% of prostate cancers in the United States progress to castration-resistant disease. The existing pharmacological therapies for metastatic and/or castration-resistant prostate cancer do not provide significant survival benefit. This review summarizes the importance of transcription factor Stat5 signaling in the pathogenesis of prostate cancer and discusses the molecular basis of Stat5a/b inhibition as a therapeutic strategy for prostate cancer." @default.
- W2059852859 created "2016-06-24" @default.
- W2059852859 creator A5034260054 @default.
- W2059852859 creator A5072652868 @default.
- W2059852859 creator A5084530020 @default.
- W2059852859 date "2010-02-01" @default.
- W2059852859 modified "2023-10-02" @default.
- W2059852859 title "Transcription factor Stat5a/b as a therapeutic target protein for prostate cancer" @default.
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