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DRUG CLASS:

HOTAIR inhibitor

Related drugs:
2ms
AQB improves carboplatin sensitivity in endometrial cancer through dual DNA repair modulation: suppression of the p21-E2F1-RAD51 and ATF3-HDAC1-BRCA1 signaling. (PubMed, Cell Death Dis)
Preferred treatment options for advanced or recurrent EC patients include a combination of carboplatin and paclitaxel, with modest clinical outcomes...This study identified the novel small-molecule inhibitor AC1Q3QWB (AQB) as a potent enhancer of carboplatin efficacy...In vivo studies using subcutaneous xenografts and a stage IV EC patient-derived xenograft (PDX) model demonstrated that AQB enhanced carboplatin's antitumor effects, reduced the required carboplatin dose, and alleviated associated toxicity. The combination of AQB with standard chemotherapy holds promise for improving outcomes in patients with advanced or recurrent EC.The schematic diagram illustrates the mechanism by which AQB enhances the sensitivity of EC cells to CBPt.
Journal • BRCA Biomarker
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BRCA1 (Breast cancer 1, early onset) • HRD (Homologous Recombination Deficiency) • RAD51 (RAD51 Homolog A) • HOTAIR (HOX Transcript Antisense RNA) • HDAC1 (Histone Deacetylase 1) • CDKN1A (Cyclin-dependent kinase inhibitor 1A) • ATF3 (Activating Transcription Factor 3) • BBC3 (BCL2 Binding Component 3) • E2F1 (E2F transcription factor 1)
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carboplatin • paclitaxel • AC1Q3QWB
2years
Compound AC1Q3QWB upregulates CDKN1A and SOX17 by interrupting the HOTAIR-EZH2 interaction and enhances the efficacy of tazemetostat in endometrial cancer. (PubMed, Cancer Lett)
Our results advocate AQB, a recently discovered small-molecule inhibitor, as a promising agent against EC cells. When combined with TAZ, it offers a novel therapeutic strategy for EC treatment.
Journal
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HOTAIR (HOX Transcript Antisense RNA) • SOX17 (SRY-Box Transcription Factor 17) • CDKN1A (Cyclin-dependent kinase inhibitor 1A)
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Tazverik (tazemetostat) • AC1Q3QWB