Drug resistance in metastatic castration-resistant prostate cancer: an update on the status quo
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OAE Publishing Inc.
Abstract
Prostate cancer (PCa) is a leading cause of cancer-related morbidity and mortality in men globally. Despite improvements in the diagnosis and treatment of PCa, a significant proportion of patients with high-risk localized disease and all patients with advanced disease at diagnosis will experience progression to metastatic castration-resistant prostate cancer (mCRPC). Multiple drugs are now approved as the standard of care treatments for patients with mCRPC that have been shown to prolong survival. Although the majority of patients will respond initially, primary and secondary resistance to these therapies make mCRPC an incurable disease. Several molecular mechanisms underlie the development of mCRPC, with the androgen receptor (AR) axis being the main driver as well as the key drug target. Understanding resistance mechanisms is crucial for discovering novel therapeutic strategies to delay or reverse the progression of the disease. In this review, we address the diverse mechanisms of drug resistance in mCRPC. In addition, we shed light on emerging targeted therapies currently being tested in clinical trials with promising potential to overcome mCRPC-drug resistance. © The Author(s) 2022.
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Keywords
Androgen receptor, Drug resistance, Mcrpc, Novel targeted therapeutics, Prostate cancer, Androgen receptor antagonist, Antibody drug conjugate, Bispecific antibody, Cancer vaccine, Cytochrome p450 family 17, Glucocorticoid receptor, Nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase inhibitor, Prostate specific membrane antigen, Radioligand, Androgen synthesis, Cancer chemotherapy, Cancer immunotherapy, Castration resistant prostate cancer, Cell differentiation, Chromatin, Chromatin assembly and disassembly, Cytotoxicity, Gene amplification, Gene overexpression, Human, Molecularly targeted therapy, Point mutation, Priority journal, Protein processing, Review, Steroidogenesis, Tumor microenvironment