AI Article Synopsis

  • High occupational exposure to vinyl chloride is linked to hepatic hemangiosarcoma, but the precise mechanisms and biomarkers are not yet established.
  • Metabolomic analysis of plasma samples from workers with this cancer revealed significant changes in 60 metabolites, with high predictive accuracy in differentiating affected individuals from controls.
  • The study identified critical metabolic pathways and potential biomarkers, suggesting a connection between vinyl chloride exposure and cancer development.

Article Abstract

Background: High-level occupational vinyl chloride (VC) exposures have been associated with hepatic hemangiosarcoma, which typically develops following a long latency period. Although VC is genotoxic, a more comprehensive mode of action has not been determined and diagnostic biomarkers have not been established. The purpose of this study is to address these knowledge gaps through plasma metabolomics.

Methods: Plasma samples from polyvinyl chloride polymerization workers who developed hemangiosarcoma (cases, = 15) and VC exposure-matched controls ( = 17) underwent metabolomic analysis. Random forest and bioinformatic analyses were performed.

Results: Cases and controls had similar demographics and routine liver biochemistries. Mass spectroscopy identified 606 known metabolites. Random forest analysis had an 82% predictive accuracy for group classification. 60 metabolites were significantly increased and 44 were decreased vs. controls. Taurocholate, bradykinin and fibrin degradation product 2 were up-regulated by greater than 80-fold. The naturally occurring anti-angiogenic phenol, 4-hydroxybenzyl alcohol, was down-regulated 5-fold. Top affected ontologies involved: (i) metabolism of bile acids, taurine, cholesterol, fatty acids and amino acids; (ii) inflammation and oxidative stress; and (iii) nicotinic cholinergic signaling.

Conclusions: The plasma metabolome was differentially regulated in polyvinyl chloride workers who developed hepatic hemangiosarcoma. Ontologies potentially involved in hemangiosarcoma pathogenesis and candidate biomarkers were identified.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150673PMC
http://dx.doi.org/10.3390/ijms22105093DOI Listing

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