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Multispecies-targeting siRNAs for the modulation of JAK1 in the skin.
Tang, Qi; Gross, Katherine Y; Fakih, Hassan H; Jackson, Samuel O; Zain U I Abideen, Mohammad; Monopoli, Kathryn R; Blanchard, Carine; Bouix-Peter, Claire; Portal, Thibaud; Harris, John E; Khvorova, Anastasia; Alterman, Julia F.
  • Tang Q; RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Gross KY; Department of Dermatology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Fakih HH; RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Jackson SO; RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Zain U I Abideen M; RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Monopoli KR; RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Blanchard C; RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
  • Bouix-Peter C; Bioinformatics and Computational Biology Program, Worcester Polytechnic Institute, Worcester, MA 01609, USA.
  • Portal T; Aldena Therapeutics, London E1 6RA, United Kingdom.
  • Harris JE; Aldena Therapeutics, London E1 6RA, United Kingdom.
  • Khvorova A; Aldena Therapeutics, London E1 6RA, United Kingdom.
  • Alterman JF; Department of Dermatology, University of Massachusetts Chan Medical School, Worcester, MA 01605, USA.
Mol Ther Nucleic Acids ; 35(1): 102117, 2024 Mar 12.
Article en En | MEDLINE | ID: mdl-38304729
ABSTRACT
Identifying therapeutic oligonucleotides that are cross-reactive to experimental animal species can dramatically accelerate the process of preclinical development and clinical translation. Here, we identify fully chemically-modified small interfering RNAs (siRNAs) that are cross-reactive to Janus kinase 1 (JAK1) in humans and a large variety of other species. We validated the identified siRNAs in silencing JAK1 in cell lines and skin tissues of multiple species. JAK1 is one of the four members of the JAK family of tyrosine kinases that mediate the signaling transduction of many inflammatory cytokine pathways. Dysregulation of these pathways is often involved in the pathogenesis of various immune disorders, and modulation of JAK family enzymes is an effective strategy in the clinic. Thus, this work may open up unprecedented opportunities for evaluating the modulation of JAK1 in many animal models of human inflammatory skin diseases. Further chemical engineering of the optimized JAK1 siRNAs may expand the utility of these compounds for treating immune disorders in additional tissues.
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