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Article type: Research Article
Authors: Hwang, Eun-Sun | Lee, Hyong Joo
Affiliations: School of Agricultural Biotechnology and Center for Agricultural Biomaterials, College of Agriculture and Life Sciences, Seoul National University, Gwanak-gu, Korea
Note: [] Address for correspondence: Hyong Joo Lee, Ph.D., Department of Food Science and Technology, School of Agricultural Biotechnology and Center for Agricultural Biomaterials, College of Agriculture and Life Sciences, Seoul National University, San 56-1, Shillim-dong, Gwanak-gu, Seoul 151-742, Republic of Korea. Tel.: +82 2 880 4853; Fax: +82 2 873 5095; E-mail: leehyjo@snu.ac.kr
Abstract: Cruciferous vegetables contain a series of relatively unique secondary metabolites of amino acids, called glucosinolates, from which isothiocyanates (ITC) can be generated. While glucosinolates are not thought to be bioactive directly, ITC appear to have anticarcinogenic activity. Sinigrin, the predominant aliphatic glucosinolate in cruciferous vegetables, is hydrolyzed to yield allylisothiocyanate (AITC), which, following absorption and metabolism in humans, is excreted in the urine as an N-acetyl-cysteine (NAC) conjugate. AITC possesses numerous biochemical and physiological activities. This study examined the induction of quinine reductase (QR) by AITC and synthetic AITC-NAC in Hepa1c1c7 murine hepatoma cells. AITC and AITC-NAC inhibited cell growth in a dose-dependent manner. The induction of QR activity and QR mRNA expression was dose-responsive over a range of 0.1–2.5 μM. AITC caused 2.0- and 3.1-fold inductions of QR with 1- and 2-μM treatments, respectively. By comparison, 1 and 2 μM AITC-NAC caused 2.9- and 3.7-fold inductions of QR, respectively. Considering the potential of ITC to prevent cancer, these results provide a basis for the use of NAC-ITC conjugates as chemopreventive agents.
Keywords: Cruciferous vegetables, allylisothiocyanate, quinone reductase, N-acetyl cysteine, chemoprevention
Journal: BioFactors, vol. 26, no. 1, pp. 7-15, 2006
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