Malemud CJ, Blumenthal DE. Protein kinase small molecule inhibitors for rheumatoid arthritis: Medicinal chemistry/clinical perspectives. World J Orthop 2014; 5(4): 496-503 [PMID: 25232525 DOI: 10.5312/wjo.v5.i4.496]
Corresponding Author of This Article
Charles J Malemud, PhD, Department of Medicine, Division of Rheumatic Diseases, The Arthritis Research Laboratory, Foley Medical Building, 2061 Cornell Road, Cleveland, OH 44106-5076, United States. cjm4@cwru.edu
Research Domain of This Article
Rheumatology
Article-Type of This Article
Topic Highlight
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
World J Orthop. Sep 18, 2014; 5(4): 496-503 Published online Sep 18, 2014. doi: 10.5312/wjo.v5.i4.496
Protein kinase small molecule inhibitors for rheumatoid arthritis: Medicinal chemistry/clinical perspectives
Charles J Malemud, David E Blumenthal
Charles J Malemud, David E Blumenthal, The Arthritis Research Laboratory, Department of Medicine, Division of Rheumatic Diseases, Case Western Reserve University, Cleveland, OH 44106-5076, United States
Charles J Malemud, David E Blumenthal, Department of Anatomy, Case Western Reserve University, Cleveland, OH 44106-5076, United States
Charles J Malemud, David E Blumenthal, School of Medicine, Division of Rheumatology, Veteran’s Administration Medical Center, Cleveland, OH 44106, United States
Author contributions: Malemud CJ and Blumenthal DE solely contributed to this paper.
Supported by A contract from Genentech/Roche Group and the Case Western Reserve University School of Medicine Visual Sciences Research Core, No. P30 EY-011373
Correspondence to: Charles J Malemud, PhD, Department of Medicine, Division of Rheumatic Diseases, The Arthritis Research Laboratory, Foley Medical Building, 2061 Cornell Road, Cleveland, OH 44106-5076, United States. cjm4@cwru.edu
Telephone: +1-216-8447846 Fax: +1-216-8442288
Received: January 11, 2014 Revised: June 5, 2014 Accepted: June 20, 2014 Published online: September 18, 2014 Processing time: 221 Days and 17 Hours
Core Tip
Core tip: Signal transduction is a regulator of gene expression in cells. Janus kinase/Signal Transducers and Activators of Transcription (JAK/STAT) signaling is activated by pro-inflammatory cytokines which contributes to immune-mediated inflammation in rheumatoid arthritis. Medicinal chemistry was employed to develop JAK small molecule inhibitors for determining their clinical efficacy in active rheumatoid arthritis patients. Tofacitinib, a JAK small molecule inhibitor, is now generally used to treat moderate to severe rheumatoid arthritis patients who have not adequately responded to disease-modifying anti-rheumatic drugs or various biologic agents. The clinical efficacy of JAK small molecule inhibitors provides the impetus for future drug discovery targeted at other signal transduction pathways in rheumatoid arthritis.
Share the Article
Malemud CJ, Blumenthal DE. Protein kinase small molecule inhibitors for rheumatoid arthritis: Medicinal chemistry/clinical perspectives. World J Orthop 2014; 5(4): 496-503 [PMID: 25232525 DOI: 10.5312/wjo.v5.i4.496]