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Zebrafish blastomere screen identifies retinoic acid suppression of MYB in adenoid cystic carcinoma.


ABSTRACT: Pluripotent cells have been used to probe developmental pathways that are involved in genetic diseases and oncogenic events. To find new therapies that would target MYB-driven tumors, we developed a pluripotent zebrafish blastomere culture system. We performed a chemical genetic screen and identified retinoic acid agonists as suppressors of c-myb expression. Retinoic acid treatment also decreased c-myb gene expression in human leukemia cells. Translocations that drive overexpression of the oncogenic transcription factor MYB are molecular hallmarks of adenoid cystic carcinoma (ACC), a malignant salivary gland tumor with no effective therapy. Retinoic acid agonists inhibited tumor growth in vivo in ACC patient-derived xenograft models and decreased MYB binding at translocated enhancers, thereby potentially diminishing the MYB positive feedback loop driving ACC. Our findings establish the zebrafish pluripotent cell culture system as a method to identify modulators of tumor formation, particularly establishing retinoic acid as a potential new effective therapy for ACC.

SUBMITTER: Mandelbaum J 

PROVIDER: S-EPMC6170170 | biostudies-literature | 2018 Oct

REPOSITORIES: biostudies-literature

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Zebrafish blastomere screen identifies retinoic acid suppression of <i>MYB</i> in adenoid cystic carcinoma.

Mandelbaum Joseph J   Shestopalov Ilya A IA   Henderson Rachel E RE   Chau Nicole G NG   Knoechel Birgit B   Wick Michael J MJ   Zon Leonard I LI  

The Journal of experimental medicine 20180912 10


Pluripotent cells have been used to probe developmental pathways that are involved in genetic diseases and oncogenic events. To find new therapies that would target <i>MYB</i>-driven tumors, we developed a pluripotent zebrafish blastomere culture system. We performed a chemical genetic screen and identified retinoic acid agonists as suppressors of <i>c-myb</i> expression. Retinoic acid treatment also decreased <i>c-myb</i> gene expression in human leukemia cells. Translocations that drive overex  ...[more]

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