Prostate cancer stem cells: the role of androgen and estrogen receptors.

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.

• 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
• Journal: Oncotarget (Oncotarget) Vol. 7 Issue 1 Pg. 193-208 (Jan 05 2016) ISSN: 1949-2553 [Electronic] United States
• PMID: 26506594 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)

Chemical References

• Androgens
• GPER1 protein, human
• Receptors, Androgen
• Receptors, Estrogen
• Receptors, G-Protein-Coupled

Topics

• Androgens (pharmacology)
• Gene Expression Regulation, Neoplastic (drug effects)
• Humans
• Male
• Models, Genetic
• Neoplastic Stem Cells (metabolism, pathology)
• Prostatic Neoplasms (genetics, metabolism, pathology)
• Receptors, Androgen (genetics, metabolism)
• Receptors, Estrogen (genetics, metabolism)
• Receptors, G-Protein-Coupled (genetics, metabolism)