Literature DB >> 18447591

Spleen tyrosine kinase: a novel target for therapeutic intervention of rheumatoid arthritis.

Malini Bajpai1, Puneet Chopra, Sunanda G Dastidar, Abhijit Ray.   

Abstract

BACKGROUND: In the last few years, significant progress has been made in understanding the pathogenic mechanisms and in defining the role of relevant cells and molecules in the pathophysiology of rheumatoid arthritis (RA). Various therapies, both biological (anti-TNF, anti-interleukins [e.g., IL-1]) and small molecule inhibitors have been explored for the treatment of RA.
OBJECTIVE: To date, no single signaling pathway inhibitor as wide acting as the corticosteroids, is known. However, treatment with corticosteroids is also associated with allied side effects. Despite a lot of efforts in the category of small molecule inhibitors, no inhibitor is available to deal with RA at both fronts (inflammation and tissue damage), without causing immense side effects.
METHOD: This present review explores the role of spleen tyrosine kinase (Syk) in the pathogenesis of RA and also discusses how it may meet the present day therapeutic requirements for the treatment of RA. This review gives an in-depth discussion on the role of Syk signaling in RA, the possibilities of using Syk as a target and also discusses the possible side effects that could be associated with its inhibition.
CONCLUSION: We propose Syk inhibition as a potential therapeutic approach for the treatment of RA.

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Year:  2008        PMID: 18447591     DOI: 10.1517/13543784.17.5.641

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  20 in total

1.  [New kinase inhibitors].

Authors:  A Rubbert-Roth
Journal:  Z Rheumatol       Date:  2012-08       Impact factor: 1.372

2.  Therapy: Spleen tyrosine kinase inhibitors--novel therapies for RA?

Authors:  José A Gómez-Puerta; Xavier Bosch
Journal:  Nat Rev Rheumatol       Date:  2011-02-08       Impact factor: 20.543

3.  [Intracellular signaling transduction pathways. Potential targets in the treatment of rheumatic diseases].

Authors:  K W Frommer; M Geyer; G S Firestein
Journal:  Z Rheumatol       Date:  2012-08       Impact factor: 1.372

Review 4.  "Go upstream, young man": lessons learned from the p38 saga.

Authors:  D Hammaker; G S Firestein
Journal:  Ann Rheum Dis       Date:  2010-01       Impact factor: 19.103

5.  Arsenic inhibits mast cell degranulation via suppression of early tyrosine phosphorylation events.

Authors:  Juyoung Shim; Rachel H Kennedy; Lisa M Weatherly; Lee M Hutchinson; Jonathan H Pelletier; Hina N Hashmi; Kayla Blais; Alejandro Velez; Julie A Gosse
Journal:  J Appl Toxicol       Date:  2016-03-28       Impact factor: 3.446

Review 6.  Role of spleen tyrosine kinase inhibitors in the management of rheumatoid arthritis.

Authors:  David L Scott
Journal:  Drugs       Date:  2011-06-18       Impact factor: 9.546

Review 7.  Cardiovascular safety of biologic therapies for the treatment of RA.

Authors:  Jeffrey D Greenberg; Victoria Furer; Michael E Farkouh
Journal:  Nat Rev Rheumatol       Date:  2011-11-15       Impact factor: 20.543

Review 8.  Emerging cell and cytokine targets in rheumatoid arthritis.

Authors:  Gerd R Burmester; Eugen Feist; Thomas Dörner
Journal:  Nat Rev Rheumatol       Date:  2013-11-12       Impact factor: 20.543

Review 9.  Intracellular signal pathways: potential for therapies.

Authors:  Melissa Mavers; Eric M Ruderman; Harris Perlman
Journal:  Curr Rheumatol Rep       Date:  2009-10       Impact factor: 4.592

Review 10.  The discovery of novel experimental therapies for inflammatory arthritis.

Authors:  Charles J Malemud
Journal:  Mediators Inflamm       Date:  2010-03-18       Impact factor: 4.711

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