Microarray analysis reveals potential mechanisms of BRMS1-mediated metastasis suppression.

Patricia J Champine, Jacob Michaelson, Bart C Weimer, Danny R Welch, Daryll B DeWald
Author Information
  1. Patricia J Champine: Center for Integrated BioSystems, Utah State University, Logan, UT 84322-4700, USA.

Abstract

We used Affymetrix microarrays to compare gene expression profiles of the metastatic parental breast cancer cell line MDA-MB-435 (435) and the non-metastatic daughter cell line created by the stable expression of the BReast cancer Metastasis Suppressor 1 (BRMS1) gene in 435 cells, MDA-MB-435-BRMS1 (435/BRMS1). Analysis of microarray data provided insight into some of the potential mechanisms by which BRMS1 inhibits tumor formation at secondary sites. Furthermore, due to the importance of the microenvironment, we also examined gene expression under different growth conditions (i.e., plus or minus serum). Expression of 565 genes was significantly (adjusted P-value <0.05) altered regardless of in vitro growth conditions. BRMS1 expression significantly increased multiple major histocompatability complex (MHC) genes and significantly decreased expression of several genes associated with protein localization and secretion. The pattern of gene expression associated with BRMS1 expression suggests that metastasis suppression may be mediated by enhanced immune recognition, altered transport, and/or secretion of metastasis-associated proteins.

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Grants

  1. R01 CA087728-07/NCI NIH HHS
  2. R01 CA087728/NCI NIH HHS
  3. CA87728/NCI NIH HHS
  4. R01 CA087728-04/NCI NIH HHS
  5. R01 CA087728-06/NCI NIH HHS
  6. R01 CA087728-05A1/NCI NIH HHS

MeSH Term

Biological Transport
Breast Neoplasms
Female
Gene Expression Profiling
Humans
Microarray Analysis
Neoplasm Metastasis
Neoplasm Proteins
Repressor Proteins
Reproducibility of Results
Reverse Transcriptase Polymerase Chain Reaction

Chemicals

BRMS1 protein, human
Neoplasm Proteins
Repressor Proteins

Word Cloud

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