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DRUG:

CADD522

i
Other names: CADD522
Associations
Trials
Company:
University of East Anglia, University of Maryland Medical System
Drug class:
RUNX2 inhibitor
Associations
Trials
7ms
RUNX2 inhibition disrupts a PAX3::FOXO1-RUNX2 feed-forward loop and dismantles oncogenic gene programs in fusion-positive rhabdomyosarcoma. (PubMed, bioRxiv)
RUNX2 inhibition reduces PAX3::FOXO1 expression and signaling, which impairs fusion-positive rhabdomyosarcoma oncogenic phenotypes. In vivo treatment with CADD522 decreased tumor growth and increased survival, indicating that RUNX2 is a promising therapeutic target.
Journal
|
FOXO1 (Forkhead box O1) • MYOD1 (Myogenic Differentiation 1) • PAX3 (Paired Box 3) • RUNX2 (RUNX Family Transcription Factor 2) • YOD1 (YOD1 Deubiquitinase)
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CADD522
almost3years
YBX1-interacting small RNAs and RUNX2 can be blocked in primary bone cancer using CADD522. (PubMed, J Bone Oncol)
In xenograft mouse models, CADD522 as a single agent without surgery significantly reduced tumour volume, increased overall and metastasis-free survival and reduced cancer-induced bone disease. Our results provide insight into PBC molecular abnormalities that have led to the identification of new targets and a new therapeutic.
Journal
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YBX1 (Y-Box Binding Protein 1) • MIR140 (MicroRNA 140) • RUNX2 (RUNX Family Transcription Factor 2)
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CADD522