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Receptor for Advanced Glycation End Products and Its Involvement in Inflammatory Diseases
The receptor for advanced glycation end products (RAGE) is a transmembrane receptor of the immunoglobulin superfamily, capable of binding a broad repertoire of ligands. RAGE-ligands interaction induces a series of signal transduction cascades and lead to the activation of transcription factor NF-κB...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786507/ https://www.ncbi.nlm.nih.gov/pubmed/24102034 http://dx.doi.org/10.1155/2013/403460 |
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author | Chuah, Yaw Kuang Basir, Rusliza Talib, Herni Tie, Tung Hing Nordin, Norshariza |
author_facet | Chuah, Yaw Kuang Basir, Rusliza Talib, Herni Tie, Tung Hing Nordin, Norshariza |
author_sort | Chuah, Yaw Kuang |
collection | PubMed |
description | The receptor for advanced glycation end products (RAGE) is a transmembrane receptor of the immunoglobulin superfamily, capable of binding a broad repertoire of ligands. RAGE-ligands interaction induces a series of signal transduction cascades and lead to the activation of transcription factor NF-κB as well as increased expression of cytokines, chemokines, and adhesion molecules. These effects endow RAGE with the role in the signal transduction from pathogen substrates to cell activation during the onset and perpetuation of inflammation. RAGE signaling and downstream pathways have been implicated in a wide spectrum of inflammatory-related pathologic conditions such as arteriosclerosis, Alzheimer's disease, arthritis, acute respiratory failure, and sepsis. Despite the significant progress in other RAGE studies, the functional importance of the receptor in clinical situations and inflammatory diseases still remains to be fully realized. In this review, we will summarize current understandings and lines of evidence on the molecular mechanisms through which RAGE signaling contributes to the pathogenesis of the aforementioned inflammation-associated conditions. |
format | Online Article Text |
id | pubmed-3786507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37865072013-10-07 Receptor for Advanced Glycation End Products and Its Involvement in Inflammatory Diseases Chuah, Yaw Kuang Basir, Rusliza Talib, Herni Tie, Tung Hing Nordin, Norshariza Int J Inflam Review Article The receptor for advanced glycation end products (RAGE) is a transmembrane receptor of the immunoglobulin superfamily, capable of binding a broad repertoire of ligands. RAGE-ligands interaction induces a series of signal transduction cascades and lead to the activation of transcription factor NF-κB as well as increased expression of cytokines, chemokines, and adhesion molecules. These effects endow RAGE with the role in the signal transduction from pathogen substrates to cell activation during the onset and perpetuation of inflammation. RAGE signaling and downstream pathways have been implicated in a wide spectrum of inflammatory-related pathologic conditions such as arteriosclerosis, Alzheimer's disease, arthritis, acute respiratory failure, and sepsis. Despite the significant progress in other RAGE studies, the functional importance of the receptor in clinical situations and inflammatory diseases still remains to be fully realized. In this review, we will summarize current understandings and lines of evidence on the molecular mechanisms through which RAGE signaling contributes to the pathogenesis of the aforementioned inflammation-associated conditions. Hindawi Publishing Corporation 2013 2013-09-11 /pmc/articles/PMC3786507/ /pubmed/24102034 http://dx.doi.org/10.1155/2013/403460 Text en Copyright © 2013 Yaw Kuang Chuah et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Chuah, Yaw Kuang Basir, Rusliza Talib, Herni Tie, Tung Hing Nordin, Norshariza Receptor for Advanced Glycation End Products and Its Involvement in Inflammatory Diseases |
title | Receptor for Advanced Glycation End Products and Its Involvement in Inflammatory Diseases |
title_full | Receptor for Advanced Glycation End Products and Its Involvement in Inflammatory Diseases |
title_fullStr | Receptor for Advanced Glycation End Products and Its Involvement in Inflammatory Diseases |
title_full_unstemmed | Receptor for Advanced Glycation End Products and Its Involvement in Inflammatory Diseases |
title_short | Receptor for Advanced Glycation End Products and Its Involvement in Inflammatory Diseases |
title_sort | receptor for advanced glycation end products and its involvement in inflammatory diseases |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786507/ https://www.ncbi.nlm.nih.gov/pubmed/24102034 http://dx.doi.org/10.1155/2013/403460 |
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