Year: 2020
Type: review
Abstract: Castration-resistant prostate cancer is the lethal form of prostate cancer and most commonly remains dependent on androgen receptor (AR) signaling. Current therapies use AR signaling inhibitors (ARSI) exemplified by abiraterone acetate, a P450c17 inhibitor, and enzalutamide, a potent AR antagonist. However, drug resistance to these agents occurs within 12-18 months and they only prolong overall survival by 3-4 months. Multiple mechanisms can contribute to ARSI drug resistance. These mechanisms can include but are not limited to germline mutations in the AR, post-transcriptional alterations in AR structure, and adaptive expression of genes involved in the intracrine biosynthesis and metabolism of androgens within the tumor. This review focuses on intracrine androgen biosynthesis, how this can contribute to ARSI drug resistance, and therapeutic strategies that can be used to surmount these resistance mechanisms.
Source: Cancer Drug Resistance
DOI: 10.20517/cdr.2020.60
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: diamond
Awards: INVESTIGATING THE MOLECULAR MECHANISMS OF ACQUIRED RESISTANCE TO BET BROMODOMAIN INHIBITORS IN CASTRATION-RESISTANT PROSTATE CANCER, G2040153736, TRANSFORMATIONAL THERAPY FOR CASTRATE- RESISTANT PROSTATE CANCER, G3622126273, G4119534169, G7086741855, Center of Excellence in Environmental Toxicology
OpenAlex ID: W3096835868
