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SM04755, a Small-molecule Inhibitor of the Wnt Pathway, As a Potential Topical Treatment for Tendinopathy

Overview
Journal J Orthop Res
Publisher Wiley
Specialty Orthopedics
Date 2020 Oct 26
PMID 33104243
Citations 13
Authors
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Abstract

The Wnt pathway is upregulated in tendinopathy, affecting inflammation and tenocyte differentiation. Given its potential role in tendinopathy, this signaling pathway may be a relevant target for treatment. The current study examined the therapeutic potential of SM04755, a topical, small-molecule Wnt pathway inhibitor, for the treatment of tendinopathy using in vitro assays and animal models. In vitro, SM04755 decreased Wnt pathway activity, induced tenocyte differentiation, and inhibited catabolic enzymes and pro-inflammatory cytokines in human mesenchymal stem cells, rat tendon-derived stem cells, and human peripheral blood mononuclear cells. Evaluation of the mechanism of action of SM04755 by biochemical profiling and computational modeling identified CDC-like kinase 2 (CLK2) and dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) as molecular targets. CLK and DYRK1A inhibition by siRNA knockdown or pharmacological inhibition induced tenocyte differentiation and reduced tenocyte catabolism. In vivo, topically applied SM04755 showed therapeutically relevant exposure in tendons with low systemic exposure and no detectable toxicity in rats. Moreover, SM04755 showed reduced tendon inflammation and evidence of tendon regeneration, decreased pain, and improved weight-bearing function in rat collagenase-induced tendinopathy models compared with vehicle control. Together, these data demonstrate that CLK2 and DYRK1A inhibition by SM04755 resulted in Wnt pathway inhibition, enhanced tenocyte differentiation and protection, and reduced inflammation. SM04755 has the potential to benefit symptoms and modify disease processes in tendinopathy.

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References
1.
Monteiro M, Ramm S, Chandrasekaran V, Boswell S, Weber E, Lidberg K . A High-Throughput Screen Identifies DYRK1A Inhibitor ID-8 that Stimulates Human Kidney Tubular Epithelial Cell Proliferation. J Am Soc Nephrol. 2018; 29(12):2820-2833. PMC: 6287872. DOI: 10.1681/ASN.2018040392. View

2.
Clevers H, Loh K, Nusse R . Stem cell signaling. An integral program for tissue renewal and regeneration: Wnt signaling and stem cell control. Science. 2014; 346(6205):1248012. DOI: 10.1126/science.1248012. View

3.
Kahn M . Can we safely target the WNT pathway?. Nat Rev Drug Discov. 2014; 13(7):513-32. PMC: 4426976. DOI: 10.1038/nrd4233. View

4.
Duncan P, Stojdl D, Marius R, Scheit K, Bell J . The Clk2 and Clk3 dual-specificity protein kinases regulate the intranuclear distribution of SR proteins and influence pre-mRNA splicing. Exp Cell Res. 1998; 241(2):300-8. DOI: 10.1006/excr.1998.4083. View

5.
Kim S, Oh H, Chang J, Kim S . Recovery of Tendon Characteristics by Inhibition of Aberrant Differentiation of Tendon-Derived Stem Cells from Degenerative Tendinopathy. Int J Mol Sci. 2020; 21(8). PMC: 7215446. DOI: 10.3390/ijms21082687. View