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Impact of p53 function on the sulfotransferase-mediated bioactivation of the alkylated polycyclic aromatic hydrocarbon 1-hydroxymethylpyrene in vitro.

Abstract
The tumor suppressor p53, encoded by TP53, is known as the "guardian of the genome." Sulfotransferases (SULTs) are involved in the metabolism of alkylated polycyclic aromatic hydrocarbons such as 1-hydroxymethylpyrene (1-HMP), which is a known substrate for SULT1A1. To investigate the impact of TP53 on the metabolic activation of 1-HMP, a panel of isogenic human colorectal HCT116 cells having TP53(+/+), TP53(+/-), or TP53(-/-) were treated with 10 μM 1-HMP for 24 hr. 1-HMP-DNA adduct formation was determined by ultraperformance liquid chromatography-tandem mass spectrometry analysis, which quantified two nucleoside adducts N2 -(1-methylpyrenyl)-2'-deoxyguanosine and N6 -(1-methylpyrenyl)-2'-deoxyadenosine. 1-HMP treatment resulted in significantly (~40-fold) higher DNA adduct levels in TP53(+/+) cells than in the other cell lines. Higher levels of 1-HMP-induced DNA adducts in TP53(+/+) cells correlated with higher basal expression of SULT1A1/3 in this cell line, but 1-HMP treatment showed no effect on the expression of this protein. These results indicate that the cellular TP53 status is linked to the SULT1A1/3-mediated bioactivation of 1-HMP, thereby broadening the spectrum of p53's targets. Environ. Mol. Mutagen., 60:752-758, 2019. © 2019 Wiley Periodicals, Inc.
AuthorsLaura E Wohak, Bernhard Monien, David H Phillips, Volker M Arlt
JournalEnvironmental and molecular mutagenesis (Environ Mol Mutagen) Vol. 60 Issue 8 Pg. 752-758 (10 2019) ISSN: 1098-2280 [Electronic] United States
PMID31102418 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2019 Wiley Periodicals, Inc.
Chemical References
  • DNA Adducts
  • Pyrenes
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • 1-hydroxymethylpyrene
  • Sulfotransferases
  • Arylsulfotransferase
  • SULT1A1 protein, human
  • monoamine-sulfating phenol sulfotransferase
Topics
  • Arylsulfotransferase (metabolism)
  • Cell Line, Tumor
  • DNA Adducts (drug effects, genetics)
  • HCT116 Cells
  • Humans
  • Pyrenes (metabolism)
  • Sulfotransferases (metabolism)
  • Tumor Suppressor Protein p53 (genetics, metabolism)

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