Gene expression changes induced by a recombinant E1-/E3- adenovirus type 5 vector in human mammary epithelial cells

Adenoviral vectors are used in transferring exogenous genes to a variety of cells and tissue types both in vitro and in vivo. Gene expression changes induced by an E1/E3-defective adenovirus vector have been studied in human mammary epithelial cells by comparing the gene expression profile in infect...

Full description

Saved in:
Bibliographic Details
Published in:Intervirology Vol. 48; no. 6; p. 350
Main Authors: Scibetta, Angelo G, Copier, John, Barrett, Angela, Chaplin, Tracy, Taylor-Papadimitriou, Joyce
Format: Journal Article
Language:English
Published: Switzerland 01-01-2005
Subjects:
Online Access:Get more information
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Adenoviral vectors are used in transferring exogenous genes to a variety of cells and tissue types both in vitro and in vivo. Gene expression changes induced by an E1/E3-defective adenovirus vector have been studied in human mammary epithelial cells by comparing the gene expression profile in infected and uninfected cells. The human mammary epithelial cell line HB2 was infected with an E1/E3-defective adenovirus type 5 vector. Total RNA was extracted from infected and uninfected cells 24 and 72 h after infection and subjected to microarray analysis using the Affymetrix U133A genomic chip system. Semiquantitative RT-PCR confirmed the regulation of genes observed by microarray analysis. The microarray analysis showed 24 and 95 transcripts to be regulated 24 and 72 h after infection, respectively. A relatively high number of genes involved in innate and inflammatory host immune responses, including interleukin-8, interleukin-6, NF-kappaB(2), RELB and fos, were induced. As expected from an E1-defective virus, changes in the expression of genes involved in the G1-S transition and in the activation of cell proliferation were not detected. Our study provides insight into the host transcriptional response following transduction of an adenoviral vector into mammary epithelial cells.
ISSN:0300-5526
DOI:10.1159/000086062