Redox Modulation of p53: Mechanisms and Functional Significance
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作者:
Kim, Do-Hee
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Seoul Natl Univ, Coll Pharm, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
Kim, Do-Hee
[1
]
Kundu, Joydeb Kumar
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Seoul Natl Univ, Coll Pharm, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
Kundu, Joydeb Kumar
[1
]
Surh, Young-Joon
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Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
Seoul Natl Univ, WCU Dept Mol Med & Biopharmaceut Sci, Grad Sch Convergence Sci & Technol, Seoul 151742, South Korea
Seoul Natl Univ, Canc Res Inst, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
Surh, Young-Joon
[1
,2
,3
]
机构:
[1] Seoul Natl Univ, Coll Pharm, Seoul 151742, South Korea
[2] Seoul Natl Univ, WCU Dept Mol Med & Biopharmaceut Sci, Grad Sch Convergence Sci & Technol, Seoul 151742, South Korea
[3] Seoul Natl Univ, Canc Res Inst, Seoul 151742, South Korea
The tumor suppressor protein p53 functions as a stress-responsive transcription factor. In response to oxidative, nitrosative, and electrophilic insults, p53 undergoes post-translational modifications, such as oxidation and covalent modification of cysteines, nitration of tyrosines, acetylation of lysines, phosphorylation of serine/threonine residues, etc. Because p53 plays a vital role in the transcriptional regulation of genes encoding proteins involved in a wide spectrum of biochemical processes including DNA repair, cell-cycle regulation, and programmed cell death, the redox-modification of p53 appears to be an important determinant of cell fate. This review highlights the redox regulation of p53 and its consequences on cellular function. (C) 2011 Wiley-Liss, Inc.
机构:
Univ Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USAUniv Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
Moos, PJ
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Edes, K
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机构:Univ Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
Edes, K
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Mullally, JE
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机构:Univ Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
Mullally, JE
;
Fitzpatrick, FA
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机构:Univ Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
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Seoul Natl Univ, Coll Pharm, Natl Res Lab Mol Carcinogenesis & Chemoprevent, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Natl Res Lab Mol Carcinogenesis & Chemoprevent, Seoul 151742, South Korea
Na, Hye-Kyung
;
Surh, Young-Joon
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Seoul Natl Univ, Coll Pharm, Natl Res Lab Mol Carcinogenesis & Chemoprevent, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Natl Res Lab Mol Carcinogenesis & Chemoprevent, Seoul 151742, South Korea
机构:
Univ Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USAUniv Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
Moos, PJ
;
Edes, K
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机构:Univ Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
Edes, K
;
Mullally, JE
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机构:Univ Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
Mullally, JE
;
Fitzpatrick, FA
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机构:Univ Utah, Dept Oncol Sci, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
机构:
Seoul Natl Univ, Coll Pharm, Natl Res Lab Mol Carcinogenesis & Chemoprevent, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Natl Res Lab Mol Carcinogenesis & Chemoprevent, Seoul 151742, South Korea
Na, Hye-Kyung
;
Surh, Young-Joon
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Seoul Natl Univ, Coll Pharm, Natl Res Lab Mol Carcinogenesis & Chemoprevent, Seoul 151742, South KoreaSeoul Natl Univ, Coll Pharm, Natl Res Lab Mol Carcinogenesis & Chemoprevent, Seoul 151742, South Korea