Journal Article

A Core MYC Gene Expression Signature Is Prominent in Basal-Like Breast Cancer but Only Partially Overlaps the Core Serum Response

Frengen, Eirik, Cole, Michael D., Pendergrass, Sarah A., Whitfield, Michael L., Cowling, Victoria H., Perou, Charles M., Chandriani, Sanjay

2009

Overview

The MYC oncogene contributes to induction and growth of many cancers but the full spectrum of the MYC transcriptional response remains unclear. Using microarrays, we conducted a detailed kinetic study of genes that respond to MYCN or MYCNDeltaMBII induction in primary human fibroblasts. In parallel, we determined the response to steady state overexpression of MYCN and MYCNDeltaMBII in the same cell type. An overlapping set of 398 genes from the two protocols was designated a 'Core MYC Signature' and used for further analysis. Comparison of the Core MYC Signature to a published study of the genes induced by serum stimulation revealed that only 7.4% of the Core MYC Signature genes are in the Core Serum Response and display similar expression changes to both MYC and serum. Furthermore, more than 50% of the Core MYC Signature genes were not influenced by serum stimulation. In contrast, comparison to a panel of breast cancers revealed a strong concordance in gene expression between the Core MYC Signature and the basal-like breast tumor subtype, which is a subtype with poor prognosis. This concordance was supported by the higher average level of MYC expression in the same tumor samples. The Core MYC Signature has clinical relevance as this profile can be used to deduce an underlying genetic program that is likely to contribute to a clinical phenotype. Therefore, the presence of the Core MYC Signature may predict clinical responsiveness to therapeutics that are designed to disrupt MYC-mediated phenotypes.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Blotting, Western / Breast cancer / Breast Neoplasms - blood / Breast Neoplasms - genetics / Breast Neoplasms - pathology / Cancer genetics / Cell culture / Cells, Cultured / Comparative analysis / Cooperation / DNA microarrays / Female / Fibroblasts / Gene amplification / Gene expression / Gene Expression Profiling / Genes / Genes, myc / Genetics / Genetics and Genomics/Gene Expression / Humans / Immunohistochemistry / Medical schools / Molecular Biology/Transcription Initiation and Activation / Myc protein / Oligonucleotide Array Sequence Analysis / Oncology / Oncology/Breast Cancer / Prognosis / Prostate cancer / Proteins / Stimulation / Studies / Toxicology / Transcription / Tumors / Wound healing