Functional crosstalk among oxidative stress and O-GlcNAc signaling pathways.
Abstract
In metazoans, thousands of intracellular proteins are modified with O-linked β-N-acetylglucosamine
(O-GlcNAc) in response to a wide range of stimuli and stresses. In particular, a complex
and evolutionarily conserved interplay between O-GlcNAcylation and oxidative stress
has emerged in recent years. Here, we review the current literature on the connections
between O-GlcNAc and oxidative stress, with a particular emphasis on major signaling
pathways, such as KEAP1/NRF2, FOXO, NFκB, p53 and cell metabolism. Taken together,
this work sheds important light on the signaling functions of protein glycosylation
and the mechanisms of stress responses alike and illuminates how the two are integrated
in animal cell physiology.
Type
Journal articlePermalink
https://hdl.handle.net/10161/19688Published Version (Please cite this version)
10.1093/glycob/cwy027Publication Info
Chen, Po-Han; Chi, Jen-Tsan; & Boyce, Michael (2018). Functional crosstalk among oxidative stress and O-GlcNAc signaling pathways. Glycobiology, 28(8). pp. 556-564. 10.1093/glycob/cwy027. Retrieved from https://hdl.handle.net/10161/19688.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Michael Scott Boyce
Associate Professor of Biochemistry
The Boyce Lab studies mammalian cell signaling through protein glycosylation. For
the latest news, project information and publications from our group, please visit
our web site at http://www.boycelab.org or follow us on Twitter at https://twitter.com/BoyceLab.
Jen-Tsan Ashley Chi
Professor in Molecular Genetics and Mirobiology
We are using functional genomic approaches to investigate the nutrient signaling and
stress adaptations of cancer cells when exposed to various nutrient deprivations and
microenvironmental stress conditions. Recently, we focus on two areas. First, we are
elucidating the genetic determinants and disease relevance of ferroptosis, a newly
recognized form of cell death. Second, we have identified the mammalian stringent
response pathway which is highly similar to bacterial stringent response, but
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