Functional crosstalk among oxidative stress and O-GlcNAc signaling pathways.

dc.contributor.author

Chen, Po-Han

dc.contributor.author

Chi, Jen-Tsan

dc.contributor.author

Boyce, Michael

dc.date.accessioned

2020-01-01T16:55:44Z

dc.date.available

2020-01-01T16:55:44Z

dc.date.issued

2018-08

dc.date.updated

2020-01-01T16:55:44Z

dc.description.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.

dc.identifier

4935241

dc.identifier.issn

0959-6658

dc.identifier.issn

1460-2423

dc.identifier.uri

https://hdl.handle.net/10161/19688

dc.language

eng

dc.publisher

Oxford University Press (OUP)

dc.relation.ispartof

Glycobiology

dc.relation.isversionof

10.1093/glycob/cwy027

dc.subject

Animals

dc.subject

Humans

dc.subject

Acetylglucosamine

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Signal Transduction

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Oxidative Stress

dc.title

Functional crosstalk among oxidative stress and O-GlcNAc signaling pathways.

dc.type

Journal article

duke.contributor.orcid

Chi, Jen-Tsan|0000-0003-3433-903X

duke.contributor.orcid

Boyce, Michael|0000-0002-2729-4876

pubs.begin-page

556

pubs.end-page

564

pubs.issue

8

pubs.organisational-group

School of Medicine

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Duke

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Duke Cancer Institute

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Molecular Genetics and Microbiology

pubs.organisational-group

Basic Science Departments

pubs.organisational-group

Pharmacology & Cancer Biology

pubs.organisational-group

Radiation Oncology

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Medicine, Rheumatology and Immunology

pubs.organisational-group

Medicine

pubs.organisational-group

Biochemistry

pubs.publication-status

Published

pubs.volume

28

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