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Oncogene. 2001 May 17;20(22):2854-8.

Global analysis of differential gene expression after transformation with the v-H-ras oncogene in a murine tumor model.

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  • 1Department of Roche Genetics, F. Hoffmann La-Roche Ltd., CH-4070 Basel, Switzerland.

Erratum in

  • Oncogene 2001 Aug 9;20(35):4916.

Abstract

Mouse PB-3c mast cells stably transfected with the v-H-ras oncogene induce tumor formation in vivo when implanted into mice. Such tumor cells are characterized by an autocrine IL-3 loop. DNA microarrays allow simultaneous transcript imaging of several thousand genes and the technique was applied in this tumor model to analyse gene expression following malignant transformation. Using three independent tumor lines derived from the same precursor the expression of about 400 out of 11 000 genes was modulated in each tumor. A subset of only 75 genes (0.68%) is shared and up- or downregulated in all three lines. A significant portion of this gene pool possesses functions related to tumorigenesis such as cell adhesion, signaling or transcriptional regulation. Apart from a number of expressed sequence tags (EST's) we find downregulation of four interferon-inducible genes in the tumor lines. Finally, when we extrapolate our data to the complete mouse genome, we estimate that about 500 genes are differentially expressed in tumor cells compared to the precursor cell PB-3c.

PMID:
11420697
[PubMed - indexed for MEDLINE]
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