RAGE: therapeutic target and biomarker of the inflammatory response--the evidence mounts.

Abstract:

:The RAGE binds multiple ligand families linked to hyperglycemia, aging, inflammation, neurodegeneration, and cancer. Activation of RAGE by its ligands stimulates diverse signaling cascades. The recent observation that the cytoplasmic domain of RAGE interacts with diaphanous or mDia-1 links RAGE signal transduction to cellular migration and activation of the Rho GTPases, cdc42 and rac-1. Pharmacological blockade of RAGE or genetic deletion of RAGE imparts significant protection in murine models of diabetes, inflammatory conditions, Alzheimer's disease, and tumors. Intriguingly, soluble forms of RAGE, including the splice variant-derived esRAGE, circulate in human plasma. Studies in human subjects suggest that sRAGE levels may be modulated by the diseases impacted by RAGE and its ligands. Thus, in addition to being a potential therapeutic target in chronic disease, monitoring of plasma sRAGE levels may provide a novel biomarker platform for tracking chronic inflammatory diseases, their severity, and response to therapeutic intervention.

journal_name

J Leukoc Biol

authors

Ramasamy R,Yan SF,Schmidt AM

doi

10.1189/jlb.0409230

subject

Has Abstract

pub_date

2009-09-01 00:00:00

pages

505-12

issue

3

eissn

0741-5400

issn

1938-3673

pii

jlb.0409230

journal_volume

86

pub_type

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