Antiandrogenic activities of diesel exhaust particle extracts in PC3/AR human prostate carcinoma cells

Ryoichi Kizu, Kazumasa Okamura, Akira Toriba, Atsushi Mizokami, Kerry L Burnstein, Carolyn M. Klinge, Kazuichi Hayakawa

Research output: Contribution to journalArticle

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Abstract

We collected diesel exhaust particles (DEPs) emitted from three diesel-engine vehicles - a car, a bus, and a truck - in daily use, and prepared DEP extracts (DEPEs), designated as EC, EB, or ET, respectively. The androgenic and antiandrogenic effects of the DEPE samples were examined by a luciferase reporter assay in human prostate carcinoma PC3/AR cells transiently transfected with a prostate specific antigen gene promoter-driven luciferase expression vector pGLPSA5.8. PC3/AR is a subline of human prostate carcinoma PC3 transformed to stably express wild-type human androgen receptor (AR). While DEPE samples did not exhibit any androgenic effect, they exerted antiandrogenic effect, inhibiting dihydrotestosterone (10 pM) -induced luciferase activity by 24 to 52% at an extract concentration of 10 μg/ml. The antiandrogenic effect was greater in the following order: ET > EB > EC. Co-treatment of PC3/AR cells with SKF-525A, a nonselective inhibitor of cytochrome P450 (CYP) enzymes, enhanced the antiandrogenic effect, indicating that the antiandrogenic effect is caused by intact species of DEPE constituents. The antiandrogenic effect of DEPE samples was reversed by α-naphthoflavone, an aryl hydrocarbon receptor (AhR) antagonist. The antiandrogenic activity of a DEPE sample correlated with its AhR agonist activity assayed in PC3/AR cells transiently transfected with CYP1A1 gene promoter-driven luciferase expression vector pLUC1A1. Equimolar mixtures of ten polycyclic aromatic hydrocarbons (PAHs) having four or more rings, structures found in the DEPEs, showed significant antiandrogenic effects and AhR agonist activity at concentrations equivalent to those found in DEPE samples. Further, DEPE samples elicited only antiandrogenic effects in recombinant yeast cells, which express β-galactosidase in response to androgen. A competitive AR binding assay showed that AR-binding constituents exist in DEPE samples, indicating that greater part of AR-binding constituents in DEPEs are AR antagonists. All these findings show that DEPE samples exhibit significant antiandrogenic effect in cell-based transcription assay and that this effect is due in part to the constituents with AhR agonist activity including PAHs and to the constituents with AR antagonist activity.

Original languageEnglish
Pages (from-to)299-309
Number of pages11
JournalToxicological Sciences
Volume76
Issue number2
DOIs
StatePublished - Dec 1 2003

Fingerprint

Vehicle Emissions
Prostate
Cells
Androgen Receptors
Carcinoma
Aryl Hydrocarbon Receptors
Luciferases
Androgen Receptor Antagonists
Assays
Polycyclic Aromatic Hydrocarbons
Motor Vehicles
Cytochrome P-450 Enzyme System
1-(2-(dodecyloxy)ethyl)pyrrolidine hydrochloride
human AR protein
Genes
Galactosidases
Proadifen
Cytochrome P-450 CYP1A1
Dihydrotestosterone
Transcription

Keywords

  • Androgen receptor
  • Antiandrogenic effect
  • Aryl hydrocarbon receptor
  • Diesel exhaust particulate
  • PC3/AR cell
  • Polycyclic aromatic hydrocarbon

ASJC Scopus subject areas

  • Toxicology

Cite this

Antiandrogenic activities of diesel exhaust particle extracts in PC3/AR human prostate carcinoma cells. / Kizu, Ryoichi; Okamura, Kazumasa; Toriba, Akira; Mizokami, Atsushi; Burnstein, Kerry L; Klinge, Carolyn M.; Hayakawa, Kazuichi.

In: Toxicological Sciences, Vol. 76, No. 2, 01.12.2003, p. 299-309.

Research output: Contribution to journalArticle

Kizu, Ryoichi ; Okamura, Kazumasa ; Toriba, Akira ; Mizokami, Atsushi ; Burnstein, Kerry L ; Klinge, Carolyn M. ; Hayakawa, Kazuichi. / Antiandrogenic activities of diesel exhaust particle extracts in PC3/AR human prostate carcinoma cells. In: Toxicological Sciences. 2003 ; Vol. 76, No. 2. pp. 299-309.
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