Oligonucleotide microarray expression analysis of genes whose expression is correlated with tumorigenic and non-tumorigenic phenotype of HeLa X humanfibroblast hybrid cells

Citation
S. Nishizuka et al., Oligonucleotide microarray expression analysis of genes whose expression is correlated with tumorigenic and non-tumorigenic phenotype of HeLa X humanfibroblast hybrid cells, CANCER LETT, 165(2), 2001, pp. 201-209
Citations number
27
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
CANCER LETTERS
ISSN journal
03043835 → ACNP
Volume
165
Issue
2
Year of publication
2001
Pages
201 - 209
Database
ISI
SICI code
0304-3835(20010426)165:2<201:OMEAOG>2.0.ZU;2-G
Abstract
In order to understand the differences and similarities between tumorigenic and non-tumorigenic HeLa x human fibroblast hybrids, gene expression profi les were examined with synthetic oligonucleotide arrays containing nearly 7 000 gene probe sets. We used two pairs of genetically related hybrids, each pair representing individual clones of non-tumorigenic and tumorigenic seg regant hybrids, respectively. Analysis of six possible comparisons, utilizi ng two algorithms, identified 204 genes with differential expression. The g reater number of differentially expressed genes was observed when non-tumor igenic hybrids were compared with tumorigenic segregants. Fifteen and 14 ge nes, respectively, were consistently found to be differentially expressed i n non-tumorigenic and tumorigenic cells. Among those 29 differentially expr essed genes, three (intestinal alkaline phosphatase, caveolin-1, and solute carrier family2, member3) have been reported previously to be associated w ith the tumorigenic phenotype, using the same hybrid pairs. In addition, am ong the genes previously detected by differential display, 78% of them exhi bited more than 5-fold change, demonstrating a high consistency between the two methods of differential gene expression. These findings suggest that s ynthetic oligonucleotide arrays are a powerful and highly reproducible tool to identify those genes whose expression is associated with certain phenot ypes. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.