Literature DB >> 18388515

Is there a future for small molecule drugs in the treatment of rheumatic diseases?

Joanna Stanczyk1, Caroline Ospelt, Steffen Gay.   

Abstract

PURPOSE OF REVIEW: In this review, we outline the landscape of recent developments regarding small molecule compounds for the treatment of inflammatory disorders by discussing drug candidates currently in the pipeline. We also stress the fact that novel techniques are available to evaluate the safety of new therapeutics at an early stage of development. RECENT
FINDINGS: Regulation of signal transduction has evolved into an important field of drug research, and small molecule inhibitors of a number of pathways are tested as new anti-inflammatory agents. For rheumatic diseases, specific Jak3 and Syk inhibitors are, so far, the most successful compounds due to their good efficacy, representing a significant advantage over p38 mitogen-activated protein kinase inhibitors. Additional benefit in the treatment of inflammatory diseases may be provided by targeting CD80, IL-12/IL-23, AP-1 transcription factor and receptors modulating cellular activation like chemokine receptors, Toll-like receptors and adenosine A3 receptor.
SUMMARY: There is a big hope that novel small molecule drugs, which are rationally designed, based on scientific advancements and biotechnological improvements, will achieve or even exceed efficacy of protein drugs. Thereby, new therapeutic alternatives would be given, and chances for improved outcomes in the care of rheumatic patients provided.

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Year:  2008        PMID: 18388515     DOI: 10.1097/BOR.0b013e3282fa13ee

Source DB:  PubMed          Journal:  Curr Opin Rheumatol        ISSN: 1040-8711            Impact factor:   5.006


  12 in total

Review 1.  Targeting non-malignant disorders with tyrosine kinase inhibitors.

Authors:  Friedrich Grimminger; Ralph T Schermuly; Hossein A Ghofrani
Journal:  Nat Rev Drug Discov       Date:  2010-12       Impact factor: 84.694

2.  Regulation of the Cell Cycle and Inflammatory Arthritis by the Transcription Cofactor LBH Gene.

Authors:  Shinji Matsuda; Deepa Hammaker; Katharyn Topolewski; Karoline J Briegel; David L Boyle; Steven Dowdy; Wei Wang; Gary S Firestein
Journal:  J Immunol       Date:  2017-08-14       Impact factor: 5.422

3.  Is there a place for nonbiological drugs in the treatment of rheumatoid arthritis?

Authors:  Alejandro Balsa; Miriam García-Arias
Journal:  Ther Adv Musculoskelet Dis       Date:  2010-12       Impact factor: 5.346

Review 4.  The role of tyrosine kinases in systemic lupus erythematosus and their potential as therapeutic targets.

Authors:  Wen-Hai Shao; Philip L Cohen
Journal:  Expert Rev Clin Immunol       Date:  2014-03-29       Impact factor: 4.473

5.  Blocking T cell co-stimulation using a CD80 blocking small molecule reduces delayed type hypersensitivity responses in rhesus monkeys.

Authors:  K G Haanstra; J Endell; D Estévâo; I Kondova; M Jonker
Journal:  Clin Exp Immunol       Date:  2009-10       Impact factor: 4.330

Review 6.  Dendritic cells as targets for therapy in rheumatoid arthritis.

Authors:  Shaukat Khan; Jeffrey D Greenberg; Nina Bhardwaj
Journal:  Nat Rev Rheumatol       Date:  2009-10       Impact factor: 20.543

Review 7.  Spleen tyrosine kinase inhibitors for rheumatoid arthritis: where are we now?

Authors:  Ian C Scott; David L Scott
Journal:  Drugs       Date:  2014-03       Impact factor: 9.546

8.  The p38 MAPK Pathway in Rheumatoid Arthritis: A Sideways Look.

Authors:  Andrew R Clark; Jonathan LE Dean
Journal:  Open Rheumatol J       Date:  2012-09-07

Review 9.  New developments in the management of psoriasis and psoriatic arthritis: a focus on apremilast.

Authors:  Andrew C Palfreeman; Kay E McNamee; Fiona E McCann
Journal:  Drug Des Devel Ther       Date:  2013-03-27       Impact factor: 4.162

Review 10.  Garden of therapeutic delights: new targets in rheumatic diseases.

Authors:  Jean M Waldburger; Gary S Firestein
Journal:  Arthritis Res Ther       Date:  2009-01-30       Impact factor: 5.156

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