Drug resistance in metastatic castration-resistant prostate cancer: an update on the status quo

dc.contributor.authorYehya, Amani
dc.contributor.authorGhamlouche, Fatima
dc.contributor.authorZahwe, Amin
dc.contributor.authorZeid, Yousef
dc.contributor.authorWakimian, Kevork
dc.contributor.authorMukherji, Deborah M.
dc.contributor.authorAbou-Kheir, Wassim G.
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Hematology Oncology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:37:19Z
dc.date.available2025-01-24T11:37:19Z
dc.date.issued2022
dc.description.abstractProstate 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.
dc.identifier.doihttps://doi.org/10.20517/cdr.2022.15
dc.identifier.eid2-s2.0-85133616439
dc.identifier.urihttp://hdl.handle.net/10938/28836
dc.language.isoen
dc.publisherOAE Publishing Inc.
dc.relation.ispartofCancer Drug Resistance
dc.sourceScopus
dc.subjectAndrogen receptor
dc.subjectDrug resistance
dc.subjectMcrpc
dc.subjectNovel targeted therapeutics
dc.subjectProstate cancer
dc.subjectAndrogen receptor antagonist
dc.subjectAntibody drug conjugate
dc.subjectBispecific antibody
dc.subjectCancer vaccine
dc.subjectCytochrome p450 family 17
dc.subjectGlucocorticoid receptor
dc.subjectNicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase inhibitor
dc.subjectProstate specific membrane antigen
dc.subjectRadioligand
dc.subjectAndrogen synthesis
dc.subjectCancer chemotherapy
dc.subjectCancer immunotherapy
dc.subjectCastration resistant prostate cancer
dc.subjectCell differentiation
dc.subjectChromatin
dc.subjectChromatin assembly and disassembly
dc.subjectCytotoxicity
dc.subjectGene amplification
dc.subjectGene overexpression
dc.subjectHuman
dc.subjectMolecularly targeted therapy
dc.subjectPoint mutation
dc.subjectPriority journal
dc.subjectProtein processing
dc.subjectReview
dc.subjectSteroidogenesis
dc.subjectTumor microenvironment
dc.titleDrug resistance in metastatic castration-resistant prostate cancer: an update on the status quo
dc.typeReview

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