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Prostate cancer stem cells: the role of androgen and estrogen receptors
Authors:Erika Di Zazzo  Giovanni Galasso  Pia Giovannelli  Marzia Di Donato  Annalisa Di Santi  Gustavo Cernera  Valentina Rossi  Ciro Abbondanza  Bruno Moncharmont  Antonio Agostino Sinisi  Gabriella Castoria  Antimo Migliaccio
Affiliation:1. Department of Biochemistry, Biophysics and General Pathology, II University of Naples, Naples, Italy;2. Department of Medicine, University of Molise, Campobasso, Italy;3. Endocrinology Section, Department of Cardio-Thoracic and Respiratory Diseases, II University of Naples, Naples, Italy
Abstract:Prostate cancer is one of the most commonly diagnosed cancers in men, and androgen deprivation therapy still represents the primary treatment for prostate cancer patients. This approach, however, frequently fails and patients develop castration-resistant prostate cancer, which is almost untreatable.Cancer cells are characterized by a hierarchical organization, and stem/progenitor cells are endowed with tumor-initiating activity. Accumulating evidence indicates that prostate cancer stem cells lack the androgen receptor and are, indeed, resistant to androgen deprivation therapy. In contrast, these cells express classical (α and/or β) and novel (GPR30) estrogen receptors, which may represent new putative targets in prostate cancer treatment.In the present review, we discuss the still-debated mechanisms, both genomic and non-genomic, by which androgen and estradiol receptors (classical and novel) mediate the hormonal control of prostate cell stemness, transformation, and the continued growth of prostate cancer. Recent preclinical and clinical findings obtained using new androgen receptor antagonists, anti-estrogens, or compounds such as enhancers of androgen receptor degradation and peptides inhibiting non-genomic androgen functions are also presented. These new drugs will likely lead to significant advances in prostate cancer therapy.
Keywords:prostate cancer   androgen receptor   estradiol receptors   GPR30   stem cells
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