GEO series
Human Uterine Serous Carcinoma cells and tumors response to CTX-439
GSE294022
Homo sapiens
Expression profiling by high throughput sequencing
32 samples
2025/12/13
GPL24676
Summary
This study aimed to investigate gene-expression alterations induced by the CDK12 inhibitor CTX-439 in uterine serous carcinoma (USC). USC cell lines (ARK1, ARK2) and patient-derived xenograft (PDX) models (USC1, USC2) were subcutaneously implanted into mice, and treated orally with either CTX-439 (CDK12 inhibitor) or vehicle control. RNA was collected from harvested tumors 6 hours after the final treatment. Differential gene expression analysis revealed significant downregulation of homologous recombination (HR)-related and DNA repair genes in CTX-439-treated groups, highlighting a potential therapeutic mechanism of action for CTX-439 in USC.
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