Literature DB >> 28416135

All the "RAGE" in lung disease: The receptor for advanced glycation endproducts (RAGE) is a major mediator of pulmonary inflammatory responses.

Elizabeth A Oczypok1, Timothy N Perkins2, Tim D Oury3.   

Abstract

The receptor for advanced glycation endproducts (RAGE) is a pro-inflammatory pattern recognition receptor (PRR) that has been implicated in the pathogenesis of numerous inflammatory diseases. It was discovered in 1992 on endothelial cells and was named for its ability to bind advanced glycation endproducts and promote vascular inflammation in the vessels of patients with diabetes. Further studies revealed that RAGE is most highly expressed in lung tissue and spurred numerous explorations into RAGE's role in the lung. These studies have found that RAGE is an important mediator in allergic airway inflammation (AAI) and asthma, pulmonary fibrosis, lung cancer, chronic obstructive pulmonary disease (COPD), acute lung injury, pneumonia, cystic fibrosis, and bronchopulmonary dysplasia. RAGE has not yet been targeted in the lungs of paediatric or adult clinical populations, but the development of new ways to inhibit RAGE is setting the stage for the emergence of novel therapeutic agents for patients suffering from these pulmonary conditions.
Copyright © 2017. Published by Elsevier Ltd.

Entities:  

Keywords:  Asthma; Bronchopulmonary dysplasia; Cystic fibrosis; Pulmonary disease; Receptor for advanced glycation endproducts (RAGE)

Mesh:

Substances:

Year:  2017        PMID: 28416135      PMCID: PMC5509466          DOI: 10.1016/j.prrv.2017.03.012

Source DB:  PubMed          Journal:  Paediatr Respir Rev        ISSN: 1526-0542            Impact factor:   2.726


  150 in total

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Journal:  J Allergy Clin Immunol       Date:  2006-10-06       Impact factor: 10.793

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4.  Alternatively spliced RAGEv1 inhibits tumorigenesis through suppression of JNK signaling.

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5.  AGEs bind to mesothelial cells via RAGE and stimulate VCAM-1 expression.

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Authors:  M A Hofmann; S Drury; B I Hudson; M R Gleason; W Qu; Y Lu; E Lalla; S Chitnis; J Monteiro; M H Stickland; L G Bucciarelli; B Moser; G Moxley; S Itescu; P J Grant; P K Gregersen; D M Stern; A M Schmidt
Journal:  Genes Immun       Date:  2002-05       Impact factor: 2.676

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7.  An Integrative Genomic Strategy Identifies sRAGE as a Causal and Protective Biomarker of Lung Function.

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Review 8.  Potential protective mechanisms of green tea polyphenol EGCG against COVID-19.

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10.  A fragment-based approach to discovery of Receptor for Advanced Glycation End products inhibitors.

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