Abstract
Prostate tumors can develop resistance to androgen receptor (AR)-targeted therapies through treatment-induced changes in transcription factor activity that promote transcriptional and morphologic features of a neuroendocrine lineage. This study identifies an unexpected role for the circadian protein ARNTL in resistance to enzalutamide, a second-generation AR-targeted therapy. See related article by Linder et al., p. 2074 (4).
Trial registration:
ClinicalTrials.gov NCT03297385.
©2022 American Association for Cancer Research.
MeSH terms
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Androgens*
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Aryl Hydrocarbon Receptor Nuclear Translocator
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Benzamides
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Circadian Rhythm
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Drug Resistance, Neoplasm / genetics
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Epigenomics
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Humans
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Male
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Nitriles
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Phenylthiohydantoin
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Prostatic Neoplasms, Castration-Resistant* / drug therapy
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Prostatic Neoplasms, Castration-Resistant* / genetics
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Prostatic Neoplasms, Castration-Resistant* / metabolism
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Receptors, Androgen / genetics
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Receptors, Androgen / metabolism
Substances
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ARNT protein, human
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Androgens
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Benzamides
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Nitriles
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Receptors, Androgen
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Aryl Hydrocarbon Receptor Nuclear Translocator
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Phenylthiohydantoin
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enzalutamide
Associated data
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ClinicalTrials.gov/NCT03297385