ZNF423 is critically required for retinoic acid-induced differentiation and is a marker of neuroblastoma outcome

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Published on Tuesday, 30 July 2013

Abstract

Retinoids play key roles in differentiation, growth arrest, and apoptosis and are increasingly being used in the clinic for the treatment of a variety of cancers, including neuroblastoma.

Here, using a large-scale RNA interference-based genetic screen, we identify ZNF423 (also known as Ebfaz, OAZ, or Zfp423) as a component critically required for retinoic acid (RA)-induced differentiation. ZNF423 associates with the RARalpha/RXRalpha nuclear receptor complex and is essential for transactivation in response to retinoids.

Downregulation of ZNF423 expression by RNA interference in neuroblastoma cells results in a growth advantage and resistance to RA-induced differentiation, whereas overexpression of ZNF423 leads to growth inhibition and enhanced differentiation.

Finally, we show that low ZNF423 expression is associated with poor disease outcome in neuroblastoma patients.

 



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Supplemental Data - Document S1



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Supplemental Data - Document S2 Table S3-S4, pdf version



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