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Abstract B04: NPM1: A new downstream effector of PI3K-AKT-mTOR pathway in prostate cancer?

Authors :
Laurent Morel
Gaelle Loubeau
Corinne Lours-Calet
Claude Beaudoin
Cyrille Dejoussineau
Rafik Boudra
Source :
Molecular Cancer Therapeutics. 14:B04-B04
Publication Year :
2015
Publisher :
American Association for Cancer Research (AACR), 2015.

Abstract

Nucleophosmin NPM1 is a molecular chaperone involved in many aspect of cellular physiology, eg. ribosomal biogenesis and cell cycle regulation. NPM1 is overexpressed in numerous types of solid tumors, including prostate cancer but the underlying molecular mechanisms are largely unknown. Using both cell lines and transgenic mouse models, we show that NPM1 expression is significantly increased in cells where the PI3K-AKT-mTOR pathway is activated through PTEN deletion. This overexpression is reversed when cells are treated with the pharmacological inhibitor of mTOR rapamycin. In accordance, transfection of small interfering RNA (siRNA) directed against mTOR leads to mTOR and NPM1 downregulation in these cells. In vivo, we found that NPM1 is overexpressed in PTEN knock-out murine prostate, and a one week treatment of these mice with rapamycin leads to NPM1 downregulation. Chromatin Immunoprecipitation (ChIP) assays show that mTOR is localized on NPM1 proximal promoter, close to a binding site for the transcription factor Ying-Yang 1 (YY1). mTOR binding on the chromatin seems to be constitutive, since rapamycin treatment did not alter its localization. mTOR could therefore regulates NPM1 expression by phosphorylating others factors involved in NPM1 gene expression, as previously described (Cunningham et al., 2007). We have previously shown that NPM1 overexpression enhance the migration and invasion abilities of prostate cancer cells (Loubeau et al., 2014). Moreover, NPM1 overexpression in mouse prostate epithelium leads to p27 protein downregulation and cyclin E upregulation, two molecular features of aggressive human prostate cancer. We thus propose that NPM1 could be a downstream effector of PI3K-AKT-mTOR pathway, supporting prostate cancer progression by altering expression of a set of genes involved in cellular homeostasis and proliferation. Citation Format: Rafik Boudra, Gaelle Loubeau, Corinne Lours-Calet, Cyrille Dejoussineau, Laurent Morel, Claude Beaudoin. NPM1: A new downstream effector of PI3K-AKT-mTOR pathway in prostate cancer? [abstract]. In: Proceedings of the AACR Special Conference: Targeting the PI3K-mTOR Network in Cancer; Sep 14-17, 2014; Philadelphia, PA. Philadelphia (PA): AACR; Mol Cancer Ther 2015;14(7 Suppl):Abstract nr B04.

Details

ISSN :
15388514 and 15357163
Volume :
14
Database :
OpenAIRE
Journal :
Molecular Cancer Therapeutics
Accession number :
edsair.doi...........7f5ba04ed1991d58c3c34dd34b0352ee
Full Text :
https://doi.org/10.1158/1538-8514.pi3k14-b04