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Maeda, S. et al.

Maeda, Otsuka, Hirata, Mitsuno, Yoshida, Shiratori, Masuho, Muramatsu , Seki, Omata,

cDNA microarray analysis of Helicobacter pylori-mediated alteration of gene expression in gastric cancer cells.

Helicobacter pylori infection stimulates several intracellular signaling pathways and is accompanied by increased gene expression in gastric epithelial cells. High-density cDNA microarray was used to characterize the mRNA expression profile of genes in human gastric cancer cells (MKN45, AGS) cocultured with H. pylori. Coculture with cag pathogenicity island (PAI)-positive H. pylori (wild-type) significantly up-regulated mRNA expression in 8 of 2304 genes tested. In 6 (interleukin-8, I(kappaB)alpha, A20, ERF-1, keratin K7, glutathione peroxidase) of the 8 genes, up-regulation was confirmed by RT-PCR. In coculture with isogenic cagE-negative mutant ((Delta)cagE), which encodes a type IV secretion system with other genes in the cag PAI, no significant up-regulation was found. We further analyzed the role of A20. Transfection of expression vector encoding A20 resulted in an inhibition of H. pylori-mediated NF-kappaB activation, indicating that H. pylori-mediated A20 expression could be a negative regulator of NF-kappaB activation. Taken together, these results indicate the importance of microarray technology as a tool for analyzing the complex interplay between H. pylori and the host.[1]

References

cDNA microarray analysis of Helicobacter pylori-mediated alteration of gene expression in gastric cancer cells. Maeda, S., Otsuka, M., Hirata, Y., Mitsuno, Y., Yoshida, H., Shiratori, Y., Masuho, Y., Muramatsu , M., Seki, N., Omata, M. Biochem. Biophys. Res. Commun. (2001) [Pubmed]

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