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Anticancer potential of CLK kinase inhibitors 1C8 and GPS167 via EMT and antiviral immune response

Anticancer potential of CLK kinase inhibitors 1C8 and GPS167 via EMT and antiviral immune response
Depletion of DHX33 antagonizes GPS167-mediated cytotoxicity. Credit: Oncotarget (2024). DOI: 10.18632/oncotarget.28585

A new research paper titled "The anticancer potential of the CLK kinases inhibitors 1C8 and GPS167 revealed by their impact on the epithelial-mesenchymal transition and the antiviral immune response" has been published in Oncotarget.

The diheteroarylamide-based compound 1C8 and the aminothiazole carboxamide-related compound GPS167 inhibit the CLK kinases, and affect the proliferation of a broad range of cancer cell lines. A chemogenomic screen previously performed with GPS167 revealed that the depletion of components associated with mitotic assembly altered sensitivity to GPS167.

In this new study, researchers from Université de Sherbrooke, Université de Lyon, Institut de recherches cliniques de Montréal, Université de Montréal, and University of British Columbia found that a similar screen performed with 1C8 also established the impact of components involved in mitotic spindle assembly.

"Accordingly, transcriptome analyses of cells treated with 1C8 and GPS167 indicated that the expression and RNA splicing of transcripts encoding mitotic spindle assembly components were affected," write the researchers.

The functional relevance of the microtubule connection was confirmed by showing that subtoxic concentrations of drugs affecting mitotic spindle assembly increased sensitivity to GPS167. 1C8 and GPS167 impacted the expression and splicing of transcripts in pathways relevant to tumor progression, including MYC targets and the epithelial mesenchymal transition (EMT). Finally, 1C8 and GPS167 altered the expression and alternative splicing of transcripts involved in the antiviral immune response. Consistent with this observation, depleting the double-stranded RNA sensor DHX33 suppressed GPS167-mediated cytotoxicity on HCT116 cells.

"Our study uncovered through which 1C8 and GPS167 affect cancer cell proliferation as well as processes critical for metastasis," the team adds.

More information: Lulzim Shkreta et al, The anticancer potential of the CLK kinases inhibitors 1C8 and GPS167 revealed by their impact on the epithelial-mesenchymal transition and the antiviral immune response, Oncotarget (2024). DOI: 10.18632/oncotarget.28585

Journal information: Oncotarget
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Citation: Anticancer potential of CLK kinase inhibitors 1C8 and GPS167 via EMT and antiviral immune response (2024, May 20) retrieved 15 June 2024 from https://medicalxpress.com/news/2024-05-anticancer-potential-clk-kinase-inhibitors.html
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