論文

査読有り 責任著者
2017年

DNA Microarray Profiling Highlights Nrf2-Mediated Chemoprevention Targeted by Wasabi-Derived Isothiocyanates in HepG2 Cells

NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL
  • Phoebe Zapanta Trio
  • ,
  • Atsuyoshi Kawahara
  • ,
  • Shunsuke Tanigawa
  • ,
  • Kozue Sakao
  • ,
  • De-Xing Hou

69
1
開始ページ
105
終了ページ
116
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1080/01635581.2017.1248296
出版者・発行元
ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD

6-MSITC and 6-MTITC are sulforaphane (SFN) analogs found in Japanese Wasabi. As we reported previously, Wasabi isothiocyanates (ITCs) are activators of Nrf2-antioxidant response element pathway, and also inhibitors of pro-inflammatory cyclooxygenase-2. This study is the first to assess the global changes in transcript levels by Wasabi ITCs, comparing with SFN, in HepG2 cells. We performed comparative gene expression profiling by treating HepG2 cells with ITCs, followed by DNA microarray analyses using HG-U133 plus 2.0 oligonucleotide array. Partial array data on selected gene products were confirmed by RT-PCR and Western blotting. Ingenuity Pathway Analysis (IPA) was used to identify functional subsets of genes and biologically significant network pathways. 6-MTITC showed the highest number of differentially altered (2 folds) gene expression, of which 114 genes were upregulated and 75 were downregulated. IPA revealed that Nrf2-mediated pathway, together with glutamate metabolism, is the common significantly modulated pathway across treatments. Interestingly, 6-MSITC exhibited the most potent effect toward Nrf2-mediated pathway. Our data suggest that 6-MSITC could exert chemopreventive role against cancer through its underlying antioxidant activity via the activation of Nrf2-mediated subsequent induction of cytoprotective genes.

リンク情報
DOI
https://doi.org/10.1080/01635581.2017.1248296
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000392619700011&DestApp=WOS_CPL
ID情報
  • DOI : 10.1080/01635581.2017.1248296
  • ISSN : 0163-5581
  • eISSN : 1532-7914
  • Web of Science ID : WOS:000392619700011

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