Experimental manipulation of radiographic density in mouse mammary gland

Extensive mammographic density in women is associated with increased risk for breast cancer. Mouse models provide a powerful approach to the study of human diseases, but there is currently no model that is suited to the study of mammographic density. We performed individual manipulations of the stro...

Full description

Saved in:
Bibliographic Details
Published inBreast cancer research : BCR Vol. 6; no. 5; pp. R540 - R545
Main Authors Hariri, Mehrdad, Wood, Geoffrey A, DiGrappa, Marco A, MacPherson, Michelle, Backman, Stephanie A, Yaffe, Martin J, Mak, Tak W, Boyd, Norman F, Khokha, Rama
Format Journal Article
LanguageEnglish
Published England National Library of Medicine - MEDLINE Abstracts 01.01.2004
BioMed Central Ltd
BioMed Central
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Extensive mammographic density in women is associated with increased risk for breast cancer. Mouse models provide a powerful approach to the study of human diseases, but there is currently no model that is suited to the study of mammographic density. We performed individual manipulations of the stromal, epithelial and matrix components of the mouse mammary gland and examined the alterations using in vivo and ex vivo radiology, whole mount staining and histology. Areas of density were generated that resembled densities in mammographic images of the human breast, and the nature of the imposed changes was confirmed at the cellular level. Furthermore, two genetic models, one deficient in epithelial structure (Pten conditional tissue specific knockout) and one with hyperplastic epithelium and mammary tumors (MMTV-PyMT), were used to examine radiographic density. Our data show the feasibility of altering and imaging mouse mammary gland radiographic density by experimental and genetic means, providing the first step toward modelling the biological processes that are responsible for mammographic density in the mouse.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1465-542X
1465-5411
1465-542X
DOI:10.1186/bcr901