## Abstract __Fat__, a candidate tumor suppressor in __Drosophila__, is a component of Hippo signaling pathway involved in controlling organ size. We found that a ∼3 Mbp deletion in mouse chromosome 3 caused tumorigenesis of a non‐tumorigenic mammary epithelial cell line. The expression of __Fat4__
Comparison of gene expression data from human and mouse breast cancers: Identification of a conserved breast tumor gene set
✍ Scribed by Andreas Klein; Ralf Wessel; Monika Graessmann; Martin Jürgens; Iver Petersen; Rita Schmutzler; Dieter Niederacher; Norbert Arnold; Alfons Meindl; Siegfried Scherneck; Susanne Seitz; Adolf Graessmann
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- French
- Weight
- 319 KB
- Volume
- 121
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The aim of our work was to establish a database for breast cancer gene expression data in order to compare human and mouse breast cancer. We identified human and mouse homologues genes and compared the expression profile of 24 human breast tumors with 6 WAP‐SVT/t breast tumors (WAP‐SVT/t animals, line 8). Our studies confirmed the heterogeneity in gene expression of human as well as mouse breast cancer cells. However, 63 genes were found to be differentially expressed (upregulated: 40; downregulated: 23 genes) in at least 75% of the breast tumors of both species. To differentiate between early and late events in tumor formation, we compared the 63 differentially expressed genes with a mouse data set obtained from hyperplastic mammary glands. This revealed that the majority of the early deregulated genes are cell proliferation specific. These early changes seem to be necessary although not sufficient for breast cancer formation. Late alterations concern mainly genes belonging to the category of cell communication and metabolism. Interestingly, most of the 63 conserved genes are commonly associated with tumorigenesis. © 2007 Wiley‐Liss, Inc.
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