4.5 Article

The association of prostatic lipids with progression, racial disparity and discovery of biomarkers in prostate cancer

期刊

TRANSLATIONAL ONCOLOGY
卷 14, 期 12, 页码 -

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.tranon.2021.101218

关键词

Prostate cancer (PCa); Lipidomics; Biomarkers; Triglyceride (TG); Cholesteryl esters (CE); Racial disparity; African American (AA); Caucasian Americans (CA); Animal model

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资金

  1. National Science Foundation
  2. K-IDeA Networks of Biomedical Research Excellence (INBRE) of National Institute of Health [P20GM103418]
  3. Kansas State University
  4. University of Mississippi Medical Center [IRSP/UMMC 68599370412, IRSP/UMMC 65101670614]
  5. National Institutes of Health/MSINBRE grant [P20RR016476]

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The study found that total lipids and neutral lipids in prostate cancer were significantly higher than in benign prostatic tissues in all populations and Caucasian American population, but not in African American population. Prostatic phospholipids were not statistically different between prostate cancer and benign prostatic tissues in all study populations. Cholesteryl ester was the only lipid class significantly higher in prostate cancer than in benign prostatic tissues in all study populations.
Background: It remains under-investigated whether prostatic lipid profiles are associated with pathogenesis, progression, racial disparity, and discovery of biomarkers in prostate cancer (PCa). Methods: The electrospray ionization-tandem mass spectrometry was applied to quantitate prostatic lipids in human and mouse PCa and non-cancer prostatic tissues. Biostatistics and bioinformatics were used to compare the concentrations of prostatic lipids at levels of total lipid, group, class and individual species between PCa and benign prostatic tissues, between races, and among pathological conditions of PCa. Results: Prostatic concentrations of total lipids as well as neutral lipids were significantly higher in PCa than in benign prostatic tissues in all population and Caucasian American population, but not in African American population. The prostatic phospholipid were not statistically different between PCa and benign prostatic tissues in all study populations. Cholesteryl ester is the only lipid class significantly higher in PCa than in benign prostatic tissues in all study populations. A panel of prostatic lipid parameters in each study population was identified as diagnostic and prognostic biomarkers with >60% of sensitivity, specificity and accuracy simultaneously. Lipid profiling on mouse prostatic tissues further confirmed correlation of prostatic lipid profiles to the pathogenesis and progression of PCa. In addition, a few prostatic lipids in mouse can serve as prognostic biomarkers in differentiation of indolent from aggressive PCa. Conclusion: The prostatic lipids are widely associated with the pathogenesis, progression and racial disparity of PCa. A panel of prostatic lipids can serve as diagnostic, prognostic and race-specific biomarkers for PCa.

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