Literature DB >> 24215346

Calpain-1 inhibitors for selective treatment of rheumatoid arthritis: what is the future?

David J Miller1, Sarah E Adams, Maurice B Hallett, Rudolf K Allemann.   

Abstract

Effective small-molecule treatment of inflammatory diseases remains an unmet need in medicine. Current treatments are either limited in effectiveness or invasive. The latest biologics prevent influx of inflammatory cells to damaged tissue. Calpain-1 is a calcium-activated cysteine protease that plays an important role in neutrophil motility. It is, therefore, a potential target for intervention in inflammatory disease. Many inhibitors of calpains have been developed but most are unselective and so unsuitable for drug use. However, recent series of α-mercaptoacrylate inhibitors target regulatory domains of calpain-1 and are much more specific. These compounds are effective in impairing the cell spreading mechanism of neutrophils in vitro and raise the possibility of treating rheumatoid arthritis with a pill; however, challenges still remain. Improved bioavailability is needed and solution of their precise mode of action should prompt the development of specific calpain-1 screens for novel classes of inhibitors.

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Year:  2013        PMID: 24215346     DOI: 10.4155/fmc.13.172

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  3 in total

1.  An unexpected co-crystal structure of the calpain PEF(S) domain with Hfq reveals a potential chaperone function of Hfq.

Authors:  Joel Cresser-Brown; Pierre Rizkallah; Yi Jin; Christian Roth; David J Miller; Rudolf K Allemann
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2020-02-05       Impact factor: 1.056

2.  Conformationally restricted calpain inhibitors.

Authors:  S E Adams; E J Robinson; D J Miller; P J Rizkallah; M B Hallett; R K Allemann
Journal:  Chem Sci       Date:  2015-08-24       Impact factor: 9.825

3.  CAPN1 promotes malignant behavior and erlotinib resistance mediated by phosphorylation of c-Met and PIK3R2 via degrading PTPN1 in lung adenocarcinoma.

Authors:  Yichuan Chen; Jingqun Tang; Ting Lu; Fang Liu
Journal:  Thorac Cancer       Date:  2020-05-12       Impact factor: 3.500

  3 in total

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