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Biomarker Initiative, Cancer Research UK Cambridge Institute, Robinson Way, Cambridge, UK
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Biomarker Initiative, Cancer Research UK Cambridge Institute, Robinson Way, Cambridge, UK
Molecular Diagnostics and Therapeutics Group, University College London, London, UK
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Astra Zeneca, 2 Riverside, Granta Park, Cambridge, UK
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Astra Zeneca, 2 Riverside, Granta Park, Cambridge, UK
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Molecular Diagnostics and Therapeutics Group, University College London, London, UK
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Biomarker Initiative, Cancer Research UK Cambridge Institute, Robinson Way, Cambridge, UK
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Molecular and Computational Diagnostics Group, Cancer Research UK Cambridge Institute, Robinson Way, Cambridge, UK
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University College Hospital at Westmoreland Street, London, UK
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Nuffield Department of Surgical Sciences, John Radcliffe Hospital, Headington, Oxford, UK
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Biomarker Initiative, Cancer Research UK Cambridge Institute, Robinson Way, Cambridge, UK
Molecular Diagnostics and Therapeutics Group, University College London, London, UK
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Introduction Prostate cancer is the leading cause of cancer death in men ( Office for National Statistics 2013 ). Prostate cancer growth relies upon androgens, such as testosterone, binding to the androgen receptor (AR) and promoting AR
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importance for metastasis of prostate cancer ( Xie et al . 2010 ). In contrast to N-cadherin, E-cadherin mediates homotypic interactions between cells, which maintain the integrity of epithelial tissues ( Giehl & Menke 2008 ). Functional studies show that N
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Introduction Prostate cancer remains the most commonly diagnosed malignancy and the second leading cause of cancer-related deaths among men in the USA ( Jemal et al. 2006 ). Gonadotrophin-releasing hormone I (GnRH I) analogue
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Department of Obstetrics and Gynecology UT Health Science Center, San Antonio, Texas, USA
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Department of Obstetrics and Gynecology UT Health Science Center, San Antonio, Texas, USA
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2007 , Girard et al . 2013 ). This review focuses on the structure, function, and genomic and extranuclear signaling of PELP1, associated signaling pathways, and its role as a target for therapeutic modulation in breast and prostate cancers. PELP1
Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada
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Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada
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Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada
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Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada
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Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada
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Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada
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Introduction Despite its initial efficacy, androgen deprivation therapy (ADT) remains a palliative treatment for metastatic prostate cancer, and patients eventually progress to castration-resistant prostate cancer (CRPC) ( So et al. 2005
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Introduction Prostate cancer is the most common malignancy and the second most common cause of cancer death in men. In the USA, there were ∼238 590 new prostate cancer diagnoses and more than 29 720 deaths in 2013 ( American Society for Cancer 2013
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decline plays a key role in the rapid loss of bone mass. Prostate cancer (Pca) is the most common cancer among people aged 60 and 70. Between the age of 75 and 79, men are six times more likely to have a high-risk Pca than men aged 55–59 ( Huynh-Le et
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Introduction Prostate cancer is the most commonly diagnosed cancer among men in the Western hemisphere, and is second only to lung cancer as a leading cause of male cancer deaths ( American Cancer Society, 2004 ). Prostate cancer is
Department of Medical Oncology, University of Sydney, Cancer Research Program, Sydney Cancer Centre, Missenden Road, Camperdown, New South Wales 2050, Australia
Department of Medical Oncology, University of Sydney, Cancer Research Program, Sydney Cancer Centre, Missenden Road, Camperdown, New South Wales 2050, Australia
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Department of Medical Oncology, University of Sydney, Cancer Research Program, Sydney Cancer Centre, Missenden Road, Camperdown, New South Wales 2050, Australia
Department of Medical Oncology, University of Sydney, Cancer Research Program, Sydney Cancer Centre, Missenden Road, Camperdown, New South Wales 2050, Australia
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Introduction Prostate cancer causes substantial morbidity and mortality worldwide ( Ferlay et al . 2004 ) and is the second leading cause of cancer death in men in developed countries ( AIHW & AACR 2008 , Jemal et al . 2009 ). Metastatic prostate
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Department of Pathology, Department of Pathology, NYU Cancer Institute, Department of Urology, Department of Pharmacology, New York Harbor Healthcare System, New York University School of Medicine, New York, New York, USA
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Department of Pathology, Department of Pathology, NYU Cancer Institute, Department of Urology, Department of Pharmacology, New York Harbor Healthcare System, New York University School of Medicine, New York, New York, USA
Department of Pathology, Department of Pathology, NYU Cancer Institute, Department of Urology, Department of Pharmacology, New York Harbor Healthcare System, New York University School of Medicine, New York, New York, USA
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Department of Pathology, Department of Pathology, NYU Cancer Institute, Department of Urology, Department of Pharmacology, New York Harbor Healthcare System, New York University School of Medicine, New York, New York, USA
Department of Pathology, Department of Pathology, NYU Cancer Institute, Department of Urology, Department of Pharmacology, New York Harbor Healthcare System, New York University School of Medicine, New York, New York, USA
Department of Pathology, Department of Pathology, NYU Cancer Institute, Department of Urology, Department of Pharmacology, New York Harbor Healthcare System, New York University School of Medicine, New York, New York, USA
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Introduction It has long been known that androgens are critical in the growth and progression of prostate cancer ( Dehm & Tindall 2006 ). Androgens signal through the androgen receptor (AR), a member of the steroid receptor family of transcription