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Mediator kinase inhibition drives myometrial stem cell differentiation and the uterine fibroid phenotype through super-enhancer reprogramming [CUT&RUN]

GSE276458 Homo sapiens Genome binding/occupancy profiling by high throughput sequencing 4 samples Submitted 2025/02/12 Platform GPL24676
Summary
Although it is known that the uterine fibroid linked MED12 mutations disrupt the CDK8/19 kinase activity, how CDK8/19 disruption contributes to making the myometrial stem cell tumorigenic and form uterine fibroids. This study seeks to determine the molecular consequences of pharmacologically disrupting mediator kinase activity in myometrial stem cells, the presumptive cell of origin for uterine fibroids, through parallel transcriptomic and epigenomic profiling by bulk RNA-seq and H3K27ac CUT&RUN.
Published in
Mediator kinase inhibition drives myometrial stem cell differentiation and the uterine fibroid phenotype through super-enhancer reprogramming
Khadka S, Lukas B, Sun CX et al. · Research square 2024 · PMID 39764110 · doi:10.21203/rs.3.rs-5125876/v1
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Also filed as BioProject PRJNA1157415 and SRA study SRP530730. Searching any of these in the dataset finder brings you back here.

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