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Location, location, location: regulation of breast cancer progression by the microenvironment

Authors
Publisher
BioMed Central
Publication Date
Source
PMC
Keywords
  • Viewpoint
Disciplines
  • Biology
  • Medicine

Abstract

279 Available online http://breast-cancer-research.com/content/6/6/279 Introduction The majority of human breast cancers arise from the transformation of epithelial cells. Numerous oncogenic events, including gene amplification, loss, and mutation, have been described that confer a growth-promoting advantage to breast tumors. A classic example of this is the identification of HER-2 amplification in a subset of breast tumors, and the successful use of anti-HER-2 directed therapy in prolonging the survival of patients with breast tumors that have HER-2 amplification. This example clearly highlights the importance of understanding the genetic changes in breast epithelial cells that are associated with breast cancer progression. However, the focus on breast epithelial cell transformation has resulted in the development of several cancer models that ignore another major regulator of breast cancer progression, namely the stroma and microenvironment. Several recent reports from both global gene expression studies and mouse models indicate that the microenvironment may be a critical modulator of breast cancer progression. Given that the microenvironment tends to be more genetically stable than breast tumor cells, it is possible that breast cancer therapies aimed at the microenvironment are less likely to develop acquired resistance. Herein I will briefly highlight several recent papers that show the importance of the microenvironment in regulation of breast cancer progression. Global gene expression studies Global gene expression patterns have revealed distinct subtypes of breast cancer, and can predict metastasis and survival. The development of gene array technology has quickly evolved to allow analysis of very small specimens derived by laser capture microdissection or cell fractionation. This has given an invaluable view of the gene expression changes within specific cell types during breast cancer progression. In this regard, Allinen and colleagues [1] performed an exhaustive analysis of ge

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