Targeting KIT by frameshifting mRNA transcripts as a therapeutic strategy for aggressive mast cell neoplasms
Snider, D. B., Arthur, G. K., Falduto, G. H., Olivera, A., Ehrhardt-Humbert, L. C., Smith, E., … Cruse, G. (2021, August 8). Molecular Therapy, Vol. 1, pp. 295–310.
MeSH headings : Humans; Mast Cells / metabolism; Mast Cells / pathology; Mastocytosis / genetics; Mastocytosis / pathology; Mastocytosis / therapy; Proto-Oncogene Proteins c-kit / genetics; RNA, Messenger / genetics; RNA, Messenger / metabolism; Receptor Protein-Tyrosine Kinases / metabolism
topics (OpenAlex): Mast cells and histamine; Polyamine Metabolism and Applications; Eosinophilic Disorders and Syndromes; Monoclonal and Polyclonal Antibodies Research
TL;DR:
It is proposed that the innovative approach, which employs well-tolerated, chemically stable oligonucleotides to target KIT expression through unconventional pathways, has potential as a KIT-targeted therapeutic alone, or in combination with agents thattarget KIT signaling, in the treatment of K IT-associated malignancies.
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