Inflammatory bowel disease - glycomics perspective.


Journal

Biochimica et biophysica acta. General subjects
ISSN: 1872-8006
Titre abrégé: Biochim Biophys Acta Gen Subj
Pays: Netherlands
ID NLM: 101731726

Informations de publication

Date de publication:
10 2019
Historique:
received: 14 01 2019
revised: 24 06 2019
accepted: 01 07 2019
pubmed: 6 7 2019
medline: 3 4 2020
entrez: 6 7 2019
Statut: ppublish

Résumé

Inflammatory bowel disease (IBD) pathogenesis is still not well understood. It is considered to result from genetic susceptibility, environment, microbiota composition and aberrant immune response. Crohn's disease (CD) and ulcerative colitis (UC), forms of IBD, are sometimes indistinguishable by typical laboratory and clinical characteristics making timely diagnosis and subsequent therapy hit-and-miss. Glycosylation has shown a promising biomarker potential for early IBD diagnosis and effective response to treatment prediction. This mini-review briefly covers present knowledge of IBD pathophysiology, with a focus on recent research on the role of glycosylation in IBD pathogenesis and disease progression. Aberrant glycosylation significantly changes functionality of key proteins in intestinal niche and is involved in IBD etiology. Elucidating mechanisms of IBD development is one of critical goals in managing this disease. Glycans are important for fine-tuning of intestinal processes that ensure homeostatic conditions which, if disrupted, lead to IBD.

Sections du résumé

BACKGROUND
Inflammatory bowel disease (IBD) pathogenesis is still not well understood. It is considered to result from genetic susceptibility, environment, microbiota composition and aberrant immune response. Crohn's disease (CD) and ulcerative colitis (UC), forms of IBD, are sometimes indistinguishable by typical laboratory and clinical characteristics making timely diagnosis and subsequent therapy hit-and-miss. Glycosylation has shown a promising biomarker potential for early IBD diagnosis and effective response to treatment prediction.
SCOPE OF REVIEW
This mini-review briefly covers present knowledge of IBD pathophysiology, with a focus on recent research on the role of glycosylation in IBD pathogenesis and disease progression.
MAJOR CONCLUSIONS
Aberrant glycosylation significantly changes functionality of key proteins in intestinal niche and is involved in IBD etiology.
GENERAL SIGNIFICANCE
Elucidating mechanisms of IBD development is one of critical goals in managing this disease. Glycans are important for fine-tuning of intestinal processes that ensure homeostatic conditions which, if disrupted, lead to IBD.

Identifiants

pubmed: 31276732
pii: S0304-4165(19)30164-3
doi: 10.1016/j.bbagen.2019.07.001
pii:
doi:

Substances chimiques

Biomarkers 0
Blood Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1595-1601

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Maja Hanić (M)

Genos Glycoscience Research Laboratory, Zagreb, Croatia. Electronic address: mhanic@genos.hr.

Irena Trbojević-Akmačić (I)

Genos Glycoscience Research Laboratory, Zagreb, Croatia. Electronic address: iakmacic@genos.hr.

Gordan Lauc (G)

Genos Glycoscience Research Laboratory, Zagreb, Croatia; University of Zagreb, Faculty of Pharmacy and Biochemistry, Zagreb, Croatia. Electronic address: glauc@pharma.hr.

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Classifications MeSH