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Identification of deregulated genes by single wall carbon-nanotubes in human normal bronchial epithelial cells

Anas Alazzamab, Etienne Mfoumouab, Ion Stiharua, Amal Kassaba, Andrew Darnelb, Amber Yasmeenb, Narayanswamy Sivakumara, Rama Bhata, Ala-Eddin Al MoustafaabcCorresponding Author Informationemail addressemail address

Received 12 May 2009; received in revised form 12 October 2009; accepted 7 December 2009. published online 07 January 2010.
Accepted Manuscript

Abstract 

In order to identify genes affected by single-wall carbon-nanotubes (SWCNTs) in human normal lung cells, we compared the gene expression profile of human normal bronchial epithelial (HNBE) cells with those SWCNTs-treated cells. A cDNA microarray analysis consisting of 54 675 human genes revealed significant changes in the expression of 14 294 genes, with 7 029 genes being up-regulated and 7 265 being down-regulated. This comprehensive list of genes included those associated with cell cycle, apoptosis, cell survival, cell adhesion and motility, signal transduction and transcription regulator. Additional analysis of 19 genes using reverse transcription (RT)-PCR supported the reliability of the microarray analysis. More specifically, our study demonstrates, for the first time, evidence that Rho GTPase-26, GTP binding protein-2, Protein phosphatase-1, Inhibin beta-E, Growth differentiation factor-15, Activating transcription factor-3 and Forkhead-a2 are up-regulated in the SWCNTs-treated HNBE cells compared to untreated cells; while Serpin peptidase inhibitor-4, Chemokine-11, Kinesins (14, 15 and 20A), Leupaxin, Repetin and Hyaluronan-mediated motility receptor are down-regulated in SWCNTs-treated HNBE cells in comparison with their control cells. These findings provide a large body of information regarding gene expression profiles associated with SWCNTs exposure in human lung bronchial epithelial cells, and also represent a source to investigate the mechanism of the effect of SWCNTs in human normal lung cells.

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a Department of Mechanical Engineering, Concordia University, Montréal, Quebec, Canada

b Montréal Centre for Experimental Therapeutics in Cancer, Lady Davis Institute for Medical Research of the Sir Mortimer B. Davis-Jewish General Hospital, McGill University, Montréal, Canada

c Syrian Research Cancer Centre of the Syrian Society against Cancer and Department of Anatomy & Embryology of the Aleppo University, Aleppo, Syria

Corresponding Author InformationCorresponding author. Montreal Centre for Experimental Therapeutics in Cancer, Lady Davis Institute for Medical Research of the SMBD-Jewish General Hospital, 3755, Ch. de la Cote Ste-Catherine, Montréal, Quebec, Canada H3T 1E2. Tel.: +514 340 8222x3104; fax: +514 340 8716.

PII: S1549-9634(10)00005-5

doi:10.1016/j.nano.2009.12.005

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