4.5 Article

Distinct Lipidomic Landscapes Associated with Clinical Stages of Urothelial Cancer of the Bladder

Journal

EUROPEAN UROLOGY FOCUS
Volume 4, Issue 6, Pages 907-915

Publisher

ELSEVIER
DOI: 10.1016/j.euf.2017.04.005

Keywords

Phospholipids; Triglycerides; Phosphatidylserine synthase; Lymphovascular invasion

Funding

  1. American Cancer Society (ACS) [127430-RSG-15-105-01-CNE]
  2. Diana Helis Henry Medical Research Foundation
  3. Alkek Center for Molecular Discovery
  4. Agilent Technologies Center of Excellence in Mass Spectrometry at Baylor College of Medicine
  5. shared Proteomics and Metabolomics core at Baylor College of Medicine
  6. CPRIT Proteomics and Metabolomics Core Facility [RP170005]
  7. Dan L. Duncan Cancer Center
  8. John S. Dunn Gulf Coast Consortium for Chemical Genomics
  9. NIH [HD007495, DK56338, P30DK081943, U24DK097153, P30 CA125123]
  10. [NIH 1RO1CA133458-01]
  11. [NIH U01 CA167234]
  12. [DOD W81XWH-12-1-0130]
  13. [NSF DMS-1161759]
  14. [NIH RCA145444A]
  15. [NSF DMS-1228164]
  16. [U01 CA111275]
  17. [NSF DMS-11617838]
  18. [RP150451]
  19. [RP170295]

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Background: The first global lipidomic profiles associated with urothelial cancer of the bladder (UCB) and its clinical stages associated with progression were identified. Objective: To identify lipidomic signatures associated with survival and different clinical stages of UCB . Design, setting, and participants: Pathologically confirmed 165 bladder-derived tissues (126 UCB, 39 benign adjacent or normal bladder tissues). UCB tissues included Ta (n = 16), T1 (n = 30), T2 (n = 43), T3 (n = 27), and T4 (n = 9); lymphovascular invasion (LVI) positive (n = 52) and negative (n = 69); and lymph node status N0 (n = 28), N1 (n = 11), N2 (n = 9), N3 (n = 3), and Nx (n = 75). Results and limitations: UCB tissues have higher levels of phospholipids and fatty acids, and reduced levels of triglycerides compared with benign tissues. A total of 59 genes associated with altered lipids in UCB strongly correlate with patient survival in an UCB public dataset. Within UCB, there was a progressive decrease in the levels of phosphatidylserine (PS), phosphatidylethanolamines (PEs), and phosphocholines, whereas an increase in the levels of diacylglycerols (DGs) with tumor stage. Transcript and protein expression of phosphatidylserine synthase 1, which converts DGs to PSs, decreased progressively with tumor stage. Levels of DGs and lyso-PEs were significantly elevated in tumors with LVI and lymph node involvement, respectively. Lack of carcinoma in situ and treatment information is the limitation of our study. Conclusions: To date, this is the first study describing the global lipidomic profiles associated with UCB and identifies lipids associated with tumor stages, LVI, and lymph node status. Our data suggest that triglycerides serve as the primary energy source in UCB, while phospholipid alterations could affect membrane structure and/or signaling associated with tumor progression. Patient summary: Lipidomic alterations identified in this study set the stage for characterization of pathways associated with these altered lipids that, in turn, could inform the development of first-of-its-kind lipid-based noninvasive biomarkers and novel therapeutic targets for aggressive urothelial cancer of the bladder. (C) 2017 European Association of Urology. Published by Elsevier B.V.

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