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Clin Cancer Res. 2009 Nov 15;15(22):7020-8. doi: 10.1158/1078-0432.CCR-09-1126. Epub 2009 Nov 3.

Activation of host wound responses in breast cancer microenvironment.

Author information

1
Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. troester@unc.edu

Abstract

PURPOSE:

Cancer progression is mediated by processes that are also important in wound repair. As a result, cancers have been conceptualized as overhealing wounds or "wounds that do not heal," and gene expression signatures reflective of wound repair have shown value as predictors of breast cancer survival. Despite the widespread acknowledgment of commonalities between host responses to wounds and host responses to cancer, the gene expression responses of normal tissue adjacent to cancers have not been well characterized.

EXPERIMENTAL DESIGN:

Using RNA extracted from histologically normal breast tissue from 107 patients, including 60 reduction mammoplasty patients and 47 cancer patients, we measured whole genome expression profiles and identified a gene expression signature that is induced in response to breast cancer.

RESULTS:

This signature represents an in vivo "wound response" signature that is differentially expressed in the normal tissue of breast cancer patients compared with those without disease and is highly accurate (at least 92% sensitivity and 98% specificity) in distinguishing diseased and nondiseased. The in vivo wound response signature is highly prognostic of breast cancer survival, and there is a strong association between the groups identified by this signature and those identified using serum-treated fibroblasts and other microenvironment-derived or microenvironment-related signatures.

CONCLUSIONS:

The prevalence of the wound response signature in histologically normal tissue adjacent to breast cancer suggests that microenvironment response is an important variable in breast cancer progression and may be an important target for clinical interventions.

PMID:
19887484
PMCID:
PMC2783932
DOI:
10.1158/1078-0432.CCR-09-1126
[Indexed for MEDLINE]
Free PMC Article

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