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Dysfunctional Lipid Metabolism-The Basis for How Genetic Abnormalities Express the Phenotype of Aggressive Prostate Cancer

Journal

CANCERS
Volume 15, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/cancers15020341

Keywords

prostate cancer; lipid metabolism; genetics; androgen deprivation

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Advanced prostate cancer has a higher mortality rate compared to localized prostate cancer, making it crucial to study its development mechanisms and potential pathways for novel treatments. Prostate cancer is the second most common cancer in men, with increasing prevalence due to an aging population. It is important to understand the evolving mechanisms of progression in order to address the significant morbidity and mortality associated with advanced prostate cancer, where treatment options are linked to lipid metabolism.
Simple Summary Advanced prostate cancer has a higher mortality rate at diagnosis compared to localised prostate cancer. As such, it is critical to understand the mechanisms of development, and potential pathways that may drive research into novel treatments. We aim to review how lipid metabolism relates to advanced prostate cancer. Prostate cancer is the second most frequent cancer in men, with increasing prevalence due to an ageing population. Advanced prostate cancer is diagnosed in up to 20% of patients, and, therefore, it is important to understand evolving mechanisms of progression. Significant morbidity and mortality can occur in advanced prostate cancer where treatment options are intrinsically related to lipid metabolism. Dysfunctional lipid metabolism has long been known to have a relationship to prostate cancer development; however, only recently have studies attempted to elucidate the exact mechanism relating genetic abnormalities and lipid metabolic pathways. Contemporary research has established the pathways leading to prostate cancer development, including dysregulated lipid metabolism-associated de novo lipogenesis through steroid hormone biogenesis and beta-oxidation of fatty acids. These pathways, in relation to treatment, have formed potential novel targets for management of advanced prostate cancer via androgen deprivation. We review basic lipid metabolism pathways and their relation to hypogonadism, and further explore prostate cancer development with a cellular emphasis.

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