Literature DB >> 15522210

Genomewide analysis of gene expression associated with Tcof1 in mouse neuroblastoma.

Michael Mogass1, Timothy P York, Lin Li, Sinitdhorn Rujirabanjerd, Rita Shiang.   

Abstract

Mutations in the Treacher Collins syndrome gene, TCOF1, cause a disorder of craniofacial development. We manipulated the levels of Tcof1 and its protein treacle in a murine neuroblastoma cell line to identify downstream changes in gene expression using a microarray platform. We identified a set of genes that have similar expression with Tcof1 as well as a set of genes that are negatively correlated with Tcof1 expression. We also showed that the level of Tcof1 and treacle expression is downregulated during differentiation of neuroblastoma cells into neuronal cells. Inhibition of Tcof1 expression by siRNA induced morphological changes in neuroblastoma cells that mimic differentiation. Thus, expression of Tcof1 and treacle synthesis play an important role in the proliferation of neuroblastoma cells and we have identified genes that may be important in this pathway.

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Year:  2004        PMID: 15522210     DOI: 10.1016/j.bbrc.2004.10.004

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

1.  Regulation of the mouse Treacher Collins syndrome homolog (Tcof1) promoter through differential repression of constitutive expression.

Authors:  Kathryn H Shows; Rita Shiang
Journal:  DNA Cell Biol       Date:  2008-11       Impact factor: 3.311

2.  Fishing the molecular bases of Treacher Collins syndrome.

Authors:  Andrea M J Weiner; Nadia L Scampoli; Nora B Calcaterra
Journal:  PLoS One       Date:  2012-01-25       Impact factor: 3.240

3.  TCOF1 coordinates oncogenic activation and rRNA production and promotes tumorigenesis in HCC.

Authors:  Chaoshen Wu; Dian Xia; Dian Wang; Shu Wang; Zhaoran Sun; Bihuai Xu; Daoyong Zhang
Journal:  Cancer Sci       Date:  2021-12-29       Impact factor: 6.716

4.  Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes.

Authors:  Mauro S Porcel de Peralta; Valeria S Mouguelar; María Antonella Sdrigotti; Felipe A A Ishiy; Roberto D Fanganiello; Maria R Passos-Bueno; Gabriela Coux; Nora B Calcaterra
Journal:  Cell Death Dis       Date:  2016-10-06       Impact factor: 8.469

  4 in total

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