Young-Joon Surh

Prof. Dr. Young-Joon Surh

Seoul National Univeristy

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 December 2003 in Nature Reviews Cancer
Verified
Journal Article
Closed access
Young-Joon SurhYoung-Joon Surh
Young-Joon Surh

1 September 2001 in Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
Verified
Journal Article
Closed access
Young-Joon SurhYoung-Joon Surh
Young-Joon Surh
KCKyung-Soo Chun
Kyung-Soo Chun
HCHyun-Ho Cha
Hyun-Ho Cha
SHSeong Su Han
Seong Su Han
YKYoung-Sam Keum
Young-Sam Keum
SLSang Sup Lee
Sang Sup Lee

20 October 2008 in Planta Medica
Verified
Journal Article
Closed access
PDF file
Young-Joon SurhYoung-Joon Surh
Young-Joon Surh
JKJoydeb Kumar Kundu
Joydeb Kumar Kundu
HNHye-Kyung Na
Hye-Kyung Na
A wide array of dietary phytochemicals have been reported to induce the expression of enzymes involved in both cellular antioxidant defenses and elimination/inactivation of electrophilic carcinogens. Induction of such cytoprotective enzymes by edible phytochemicals largely accounts for their cancer chemopreventive and chemoprotective activities. Nuclear factor-erythroid-2-related factor 2 (Nrf2) plays a crucial role in the coordinated induction of those genes encoding many stress-responsive and cytoptotective enzymes and related proteins. These include NAD(P)H:quinone oxidoreductase-1, heme oxygenase-1, glutamate cysteine ligase, glutathione S-transferase, glutathione peroxidase, thioredoxin, etc. In resting cells, Nrf2 is sequestered in the cytoplasm as an inactive complex with the repressor Kelch-like ECH-associated protein 1 (Keap1). The release of Nrf2 from its repressor is most likely to be achieved by alterations in the structure of Keap1. Keap1 contains several reactive cysteine residues that function as sensors of cellular redox changes. Oxidation or covalent modification of some of these critical cysteine thiols would stabilize Nrf2, thereby facilitating nuclear accumulation of Nrf2. After translocation into nucleus, Nrf2 forms a heterodimer with other transcription factors, such as small Maf, which in turn binds to the 5′-upstream cis-acting regulatory sequence, termed antioxidant response elements (ARE) or electrophile response elements (EpRE), located in the promoter region of genes encoding various antioxidant and phase 2 detoxifying enzymes. Certain dietary chemopreventive agents target Keap1 by oxidizing or chemically modifying one or more of its specific cysteine thiols, thereby stabilizing Nrf2. In addition, phosphorylation of specific serine or threonine residues present in Nrf2 by upstream kinases may also facilitate the nuclear localization of Nrf2. Multiple mechanisms of Nrf2 activation by signals mediated by one or more of the upstream kinases, such as mitogen-activated protein kinases, phosphatidylionositol-3-kinase/Akt, protein kinase C, and casein kinase-2 have recently been proposed. This review highlights the cytoprotective gene expression induced by some representative dietary chemopreventive phytochemicals with the Nrf2-Keap1 system as a prime molecular target.

1 July 1999 in Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
Verified
Journal Article
Closed access
Young-Joon SurhYoung-Joon Surh
Young-Joon Surh


14 February 2005 in Oncogene
Verified
Journal Article
Closed access
SKSue Ok Kim
Sue Ok Kim
JKJoydeb Kumar Kundu
Joydeb Kumar Kundu
Young Kee ShinYoung Kee Shin
Young Kee Shin
JPJin-Hong Park
Jin-Hong Park
MCMyung-Haing Cho
Myung-Haing Cho
Young-Joon SurhYoung-Joon Surh
Young-Joon Surh