Literature DB >> 33515704

Emerging roles of protein O-GlcNAcylation in cardiovascular diseases: Insights and novel therapeutic targets.

Israel Olapeju Bolanle1, Kirsten Riches-Suman2, Ritchie Williamson3, Timothy M Palmer4.   

Abstract

Cardiovascular diseases (CVDs) are the leading cause of death globally. While the major focus of pharmacological and non-pharmacological interventions has been on targeting disease pathophysiology and limiting predisposing factors, our understanding of the cellular and molecular mechanisms underlying the pathogenesis of CVDs remains incomplete. One mechanism that has recently emerged is protein O-GlcNAcylation. This is a dynamic, site-specific reversible post-translational modification of serine and threonine residues on target proteins and is controlled by two enzymes: O-linked β-N-acetylglucosamine transferase (OGT) and O-linked β-N-acetylglucosaminidase (OGA). Protein O-GlcNAcylation alters the cellular functions of these target proteins which play vital roles in pathways that modulate vascular homeostasis and cardiac function. Through this review, we aim to give insights on the role of protein O-GlcNAcylation in cardiovascular diseases and identify potential therapeutic targets in this pathway for development of more effective medicines to improve patient outcomes.
Copyright © 2021 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  (R)-N-(Furan-2-ylmethyl)-2-(2-methoxyphenyl)-2-(2-oxo-1,2-dihydroquinoline-6-sulfonamido)-N-(thiophen-2-ylmethyl)acetamide [OSMI-1] (PubChem CID: 118634407); 2-(2-Amino-3-methoxyphenyl)-4H-chromen-4-one [PD98059] (PubChem CID: 4713); 5H-Pyrano[3,2-d]thiazole-6,7-diol, 2-(ethylamino)-3a,6,7,7a-tetrahydro-5-(hydroxymethyl)-(3aR,5R,6S,7R,7aR) [Thiamet-G] (PubChem CID: 1355663540); 6-Diazo-5-oxo-l-norleucine [DON] (PubChem CID: 9087); Alloxan (PubChem CID: 5781); Azaserine (PubChem CID: 460129); BADGP, Benzyl-2-acetamido-2-deoxy-α-d-galactopyranoside [BADGP] (PubChem CID: 561184); Cardiovascular disease; Methoxybenzene-sulfonamide [KN-93] (PubChem CID: 5312122); N-[(5S,6R,7R,8R)-6,7-Dihydroxy-5-(hydroxymethyl)-2-(2-phenylethyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-8-yl]-2-methylpropanamide [GlcNAcstatin] (PubChem CID: 122173013); O-(2-Acetamido-2-deoxy-d-glucopyranosyliden)amino-N-phenylcarbamate [PUGNAc] (PubChem CID: 9576811); O-GlcNAc transferase; O-GlcNAcase; Protein O-GlcNAcylation; Streptozotocin (PubCHem CID: 7067772)

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Year:  2021        PMID: 33515704     DOI: 10.1016/j.phrs.2021.105467

Source DB:  PubMed          Journal:  Pharmacol Res        ISSN: 1043-6618            Impact factor:   7.658


  4 in total

Review 1.  Methods for Studying Site-Specific O-GlcNAc Modifications: Successes, Limitations, and Important Future Goals.

Authors:  Stuart P Moon; Afraah Javed; Eldon R Hard; Matthew R Pratt
Journal:  JACS Au       Date:  2021-12-15

2.  O-GlcNAcylation Is Essential for Rapid Pomc Expression and Cell Proliferation in Corticotropic Tumor Cells.

Authors:  Logan J Massman; Michael Pereckas; Nathan T Zwagerman; Stephanie Olivier-Van Stichelen
Journal:  Endocrinology       Date:  2021-12-01       Impact factor: 4.736

Review 3.  Targeting Protein O-GlcNAcylation, a Link between Type 2 Diabetes Mellitus and Inflammatory Disease.

Authors:  Israel Olapeju Bolanle; Timothy M Palmer
Journal:  Cells       Date:  2022-02-17       Impact factor: 6.600

4.  O-GlcNAcylation regulates epidermal growth factor receptor intracellular trafficking and signaling.

Authors:  Liming Wu; Yaxian Cheng; Didi Geng; Zhiya Fan; Bingyi Lin; Qiang Zhu; Jingchao Li; Weijie Qin; Wen Yi
Journal:  Proc Natl Acad Sci U S A       Date:  2022-03-03       Impact factor: 12.779

  4 in total

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