Literature DB >> 20459381

RAGE: a multi-ligand receptor unveiling novel insights in health and disease.

P Alexiou1, M Chatzopoulou, K Pegklidou, V J Demopoulos.   

Abstract

Receptor for advanced glycation end products (RAGE) is expressed in a range of cell types such as endothelial cells, smooth muscle cells, mesangial cells, mononuclear phagocytes and certain neurons. It is a multi-ligand receptor and a member of the immunoglobulin superfamily of cell surface molecules. Its repertoire of ligands includes advanced glycation end products (AGEs), amyloid fibrils, amphoterin and S100/calgranulins. This variety of ligands allows RAGE to be implicated in a wide spectrum of pathological conditions such as diabetes and its complications, Alzheimer's disease, cancer and inflammation. Additionally, genetic polymorphisms in the RAGE gene may have impact on the functional activity of the receptor. It becomes obvious that RAGE pathway is a complicated one and the question of whether blockade of RAGE is a feasible and safe strategy for the prevention/treatment of chronic diseases is gradually gaining the attention of the pharmaceutical community. In this review the biology of RAGE and the triggered signaling cascades involved in health and disease will be presented. Additionally, its potential as an attractive pharmacotherapeutic target will be explored by pointing out the pharmacotherapeutic agents that have been developed for RAGE blockade.

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Year:  2010        PMID: 20459381     DOI: 10.2174/092986710791331086

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  42 in total

1.  Is the Gly82Ser polymorphism in the RAGE gene relevant to schizophrenia and the personality trait psychoticism?

Authors:  Petra Suchankova; Jonas Klang; Carin Cavanna; Göran Holm; Staffan Nilsson; Erik G Jönsson; Agneta Ekman
Journal:  J Psychiatry Neurosci       Date:  2012-02       Impact factor: 6.186

2.  M2 macrophages do not fly into a "RAGE".

Authors:  Armando Rojas; Carolina Añazco; Paulina Araya
Journal:  Inflamm Res       Date:  2016-10-03       Impact factor: 4.575

3.  Distinct dendritic cell subsets dictate the fate decision between effector and memory CD8(+) T cell differentiation by a CD24-dependent mechanism.

Authors:  Taeg S Kim; Stacey A Gorski; Steven Hahn; Kenneth M Murphy; Thomas J Braciale
Journal:  Immunity       Date:  2014-03-13       Impact factor: 31.745

4.  IL-1β, RAGE and FABP4: targeting the dynamic trio in metabolic inflammation and related pathologies.

Authors:  Aimalie L Hardaway; Izabela Podgorski
Journal:  Future Med Chem       Date:  2013-06       Impact factor: 3.808

Review 5.  Oxidative stress and β-amyloid protein in Alzheimer's disease.

Authors:  Zhiyou Cai; Bin Zhao; Anna Ratka
Journal:  Neuromolecular Med       Date:  2011-09-08       Impact factor: 3.843

6.  Effect of chronic hypoxia on RAGE and its soluble forms in lungs and plasma of mice.

Authors:  P Gopal; H R Gosker; C C de Theije; I M Eurlings; D R Sell; V M Monnier; N L Reynaert
Journal:  Biochim Biophys Acta       Date:  2015-02-19

7.  Identification of pheophorbide a as an inhibitor of receptor for advanced glycation end products in Mallotus japonicus.

Authors:  Teruki Matsumoto; Michiyo Matsuno; Norihito Ikui; Yoshiyuki Mizushina; Yume Omiya; Rikako Ishibashi; Taro Ueda; Hajime Mizukami
Journal:  J Nat Med       Date:  2021-02-24       Impact factor: 2.343

8.  Co-expression of RAGE and HMGB1 is associated with cancer progression and poor patient outcome of prostate cancer.

Authors:  Chu-Biao Zhao; Ji-Ming Bao; Yong-Jie Lu; Tong Zhao; Xin-Hua Zhou; Da-Yong Zheng; Shan-Chao Zhao
Journal:  Am J Cancer Res       Date:  2014-07-16       Impact factor: 6.166

9.  Systemic biomarkers of inflammation, oxidative stress and tissue injury and repair among waterpipe, cigarette and dual tobacco smokers.

Authors:  Naushad Ahmad Khan; Gina Lawyer; Samantha McDonough; Qixin Wang; Noura O Kassem; Flora Kas-Petrus; Dongxia Ye; Kameshwar P Singh; Nada Of Kassem; Irfan Rahman
Journal:  Tob Control       Date:  2019-09-07       Impact factor: 7.552

10.  HMGB1 enhances the protumoral activities of M2 macrophages by a RAGE-dependent mechanism.

Authors:  Armando Rojas; Fernando Delgado-López; Ramón Perez-Castro; Ileana Gonzalez; Jacqueline Romero; Israel Rojas; Paulina Araya; Carolina Añazco; Erik Morales; Jorge Llanos
Journal:  Tumour Biol       Date:  2015-10-06
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