Literature DB >> 12453678

Receptor for advanced glycation endproducts: a multiligand receptor magnifying cell stress in diverse pathologic settings.

David Stern1, Shi Du Yan, Shi Fang Yan, Ann Marie Schmidt.   

Abstract

Receptor for Advanced Glycation Endproducts (RAGE) is a member of the immunoglobulin superfamily of cell surface molecules capable of interacting with a broad spectrum of ligands, including advanced glycation endproducts (AGEs), amyloid fibrils, S100/calgranulins and amphoterin. The biology of RAGE is dictated by the accumulation of these ligands at pathologic sites, leading to upregulation of the receptor and sustained RAGE-dependent cell activation eventuating in cellular dysfunction. Although RAGE is not central to the initial pathogenesis of disorders in which it ultimately appears to be involved, such as diabetes, amyloidoses, inflammatory conditions and tumors (each of these conditions leading to accumulation of RAGE ligands), the receptor functions as a progression factor driving cellular dysfunction and exaggerating the host response towards tissue destruction, rather than restitution of homeostasis. These observations suggest that RAGE might represent a therapeutic target in a diverse group of seemingly unrelated disorders linked only by a multiligand receptor with an unusually wide and diverse repertoire of ligands, namely, RAGE. Copyright 2002 Elsevier Science B.V.

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Year:  2002        PMID: 12453678     DOI: 10.1016/s0169-409x(02)00160-6

Source DB:  PubMed          Journal:  Adv Drug Deliv Rev        ISSN: 0169-409X            Impact factor:   15.470


  79 in total

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2.  The Research on the Relationship of RAGE, LRP-1, and Aβ Accumulation in the Hippocampus, Prefrontal Lobe, and Amygdala of STZ-Induced Diabetic Rats.

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3.  Decreased levels of soluble receptor for advanced glycation end products in patients with primary Sjögren's syndrome.

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Journal:  Rheumatol Int       Date:  2008-01-30       Impact factor: 2.631

4.  Effect of cromolyn on S100P interactions with RAGE and pancreatic cancer growth and invasion in mouse models.

Authors:  Thiruvengadam Arumugam; Vijaya Ramachandran; Craig D Logsdon
Journal:  J Natl Cancer Inst       Date:  2006-12-20       Impact factor: 13.506

5.  Oleate, not ligands of the receptor for advanced glycation end-products, promotes proliferation of human arterial smooth muscle cells.

Authors:  C B Renard; B Askari; L A Suzuki; F Kramer; K E Bornfeldt
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Review 6.  High-mobility group box 1 (HMGB1) in childhood: from bench to bedside.

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7.  NF-kappaB as a molecular link between psychosocial stress and organ dysfunction.

Authors:  A Bierhaus; P M Humpert; P P Nawroth
Journal:  Pediatr Nephrol       Date:  2004-08-20       Impact factor: 3.714

Review 8.  Advanced glycation endproduct crosslinking in the cardiovascular system: potential therapeutic target for cardiovascular disease.

Authors:  Susan J Zieman; David A Kass
Journal:  Drugs       Date:  2004       Impact factor: 9.546

9.  Effects of MMP-9 inhibition by doxycycline on proteome of lungs in high tidal volume mechanical ventilation-induced acute lung injury.

Authors:  Adrian Doroszko; Thomas S Hurst; Dorota Polewicz; Jolanta Sawicka; Justyna Fert-Bober; David H Johnson; Grzegorz Sawicki
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10.  Fas (CD95) induces rapid, TLR4/IRAK4-dependent release of pro-inflammatory HMGB1 from macrophages.

Authors:  Feng Wang; Ziyue Lu; Michael Hawkes; Huan Yang; Kevin C Kain; W Conrad Liles
Journal:  J Inflamm (Lond)       Date:  2010-06-17       Impact factor: 4.981

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