Redox regulation of glutathione S-transferase induction by benzyl isothiocyanate: Correlation of enzyme induction with the formation of reactive oxygen intermediates

Yoshimasa Nakamura, Hajime Ohigashi, Seiji Masuda, Akira Murakami, Yasujiro Morimitsu, Yoshiyuki Kawamoto, Toshihiko Osawa, Masayoshi Imagawa, Koji Uchida

Research output: Contribution to journalArticle

134 Citations (Scopus)

Abstract

Here we report the molecular mechanism underlying the induction of glutathione S-transferase (GST) in rat liver epithelial RL34 cells treated with a cancer chemopreventive isothiocyanate compound, benzylisothiocyanate (BITC). BITC was found to significantly induce GST activity in RL34 cells. Northern and Western blot analyses demonstrated that BITC specifically enhanced the production of the class π GST isozyme (GSTP1). Our studies demonstrated for the first time that the addition of BITC to the cells resulted in an immediate increase in the reactive oxygen intermediates (ROIs) detected by a fluorescence probe, 2',7'-dichlorofluorescin diacetate. The level of the ROIs in the cells treated with BITC (10 μM) was ~50-fold higher than those in the control cells. Furthermore, glutathione depletion by diethyl maleate significantly enhanced BITC-induced ROI production and accelerated the BITC-induced elevation of the GST activity, whereas pretreatment of the cells with glutathione inhibited both the ROI production and GST induction. The structure-activity relationship of the isothiocyanates also indicated that the ROI-producing activities closely correlated with their GST-inducing potencies. Moreover, the GSTP1 enhancer 1-containing region was found to be essential for induction of the GSTP1 gene by intracellular ROI inducers such as BITC and diethyl maleate. These data suggest the involvement of the redox regulation on the induction of GSTP1 by BITC.

Original languageEnglish
Pages (from-to)219-225
Number of pages7
JournalCancer Research
Volume60
Issue number2
Publication statusPublished - Jan 15 2000
Externally publishedYes

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Enzyme Induction
Glutathione Transferase
Oxidation-Reduction
Oxygen
diethyl maleate
Glutathione
Isothiocyanates
benzyl isothiocyanate
Structure-Activity Relationship
Northern Blotting
Isoenzymes
Fluorescence
Western Blotting
Epithelial Cells
Liver

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Redox regulation of glutathione S-transferase induction by benzyl isothiocyanate : Correlation of enzyme induction with the formation of reactive oxygen intermediates. / Nakamura, Yoshimasa; Ohigashi, Hajime; Masuda, Seiji; Murakami, Akira; Morimitsu, Yasujiro; Kawamoto, Yoshiyuki; Osawa, Toshihiko; Imagawa, Masayoshi; Uchida, Koji.

In: Cancer Research, Vol. 60, No. 2, 15.01.2000, p. 219-225.

Research output: Contribution to journalArticle

Nakamura, Y, Ohigashi, H, Masuda, S, Murakami, A, Morimitsu, Y, Kawamoto, Y, Osawa, T, Imagawa, M & Uchida, K 2000, 'Redox regulation of glutathione S-transferase induction by benzyl isothiocyanate: Correlation of enzyme induction with the formation of reactive oxygen intermediates', Cancer Research, vol. 60, no. 2, pp. 219-225.
Nakamura, Yoshimasa ; Ohigashi, Hajime ; Masuda, Seiji ; Murakami, Akira ; Morimitsu, Yasujiro ; Kawamoto, Yoshiyuki ; Osawa, Toshihiko ; Imagawa, Masayoshi ; Uchida, Koji. / Redox regulation of glutathione S-transferase induction by benzyl isothiocyanate : Correlation of enzyme induction with the formation of reactive oxygen intermediates. In: Cancer Research. 2000 ; Vol. 60, No. 2. pp. 219-225.
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