4.5 Article

Aberrations in circulating ceramide levels are associated with poor clinical outcomes across localised and metastatic prostate cancer

Journal

PROSTATE CANCER AND PROSTATIC DISEASES
Volume 24, Issue 3, Pages 860-870

Publisher

SPRINGERNATURE
DOI: 10.1038/s41391-021-00338-z

Keywords

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Funding

  1. National Health and Medical Research Council of Australia [GNT0614296]
  2. Cancer Institute New South Wales [2018/TPG001, 10/TPG/1-04]
  3. Australian Prostate Cancer Research Centre-New South Wales
  4. Australian Department of Health and Aging
  5. Movember Foundation
  6. Prostate Cancer Foundation of Australia [MRTA3]
  7. Cancer Council New South Wales [PG 10-01]
  8. Cancer Council South Australia [PRF1117]
  9. Victorian Government's Operational Infrastructure Support Program
  10. National Institutes of Health [RO1CA212097]

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Elevated circulating ceramide species are associated with poorer clinical outcomes in prostate cancer patients, and these circulating lipid profiles could be used to predict therapeutic efficacy at different stages of PC.
Background Dysregulated lipid metabolism is associated with more aggressive pathology and poorer prognosis in prostate cancer (PC). The primary aim of the study is to assess the relationship between the plasma lipidome and clinical outcomes in localised and metastatic PC. The secondary aim is to validate a prognostic circulating 3-lipid signature specific to metastatic castration-resistant PC (mCRPC). Patients and methods Comprehensive lipidomic analysis was performed on pre-treatment plasma samples from men with localised PC (N = 389), metastatic hormone-sensitive PC (mHSPC)(N = 44), or mCRPC (validation cohort, N = 137). Clinical outcomes from our previously published mCRPC cohort (N = 159) that was used to derive the prognostic circulating 3-lipid signature, were updated. Associations between circulating lipids and clinical outcomes were examined by Cox regression and latent class analysis. Results Circulating lipid profiles featuring elevated levels of ceramide species were associated with metastatic relapse in localised PC (HR 5.80, 95% CI 3.04-11.1, P = 1 x 10(-6)), earlier testosterone suppression failure in mHSPC (HR 3.70, 95% CI 1.37-10.0, P = 0.01), and shorter overall survival in mCRPC (HR 2.54, 95% CI 1.73-3.72, P = 1 x 10(-6)). The prognostic significance of circulating lipid profiles in localised PC was independent of standard clinicopathological and metabolic factors (P < 0.0002). The 3-lipid signature was verified in the mCRPC validation cohort (HR 2.39, 95% CI 1.63-3.51, P = 1 x 10(-5)). Conclusions Elevated circulating ceramide species are associated with poorer clinical outcomes across the natural history of PC. These clinically actionable lipid profiles could be therapeutically targeted in prospective clinical trials to potentially improve PC outcomes.

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