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Abnormal Mammary Adipose Tissue Environment of Brca1 Mutant Mice Show a Persistent Deposition of Highly Vascularized Multilocular Adipocytes | OMICS International | Abstract
ISSN: 1948-5956

Journal of Cancer Science & Therapy
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Research Article

Abnormal Mammary Adipose Tissue Environment of Brca1 Mutant Mice Show a Persistent Deposition of Highly Vascularized Multilocular Adipocytes

Laundette P. Jones1*, Destiney Buelto2, Elaine Tago3 and Kwadwo E. Owusu-Boaitey4

1Department of Pharmacology and Experimental Therapeutics, University of Maryland, Baltimore, School of Medicine, Baltimore, MD 21201

2Department of Biology, University of North Carolina, Chapel Hill, Chapel Hill, NC 27599

3American Samoa Community College, P.O. Box 4104, Pago Pago, American Samoa 96799

4Department of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250

*Corresponding Author:
Laundette P. Jones, PhD
University of Maryland, Baltimore
Bressler Bldg., Rm 4-002, 655 W. Baltimore Street
Baltimore MD 21201, USA
Tel: 410-706-7331
Fax: 410-706-0032
E-mail: [email protected]

Received Date: November 23, 2011; Accepted Date: December 06, 2011; Published Date: December 08, 2011

Citation: Jones LP, Buelto D, Tago E, Owusu-Boaitey KE (2011) Abnormal Mammary Adipose Tissue Environment of Brca1 Mutant Mice Show a Persistent Deposition of Highly Vascularized Multilocular Adipocytes. J Cancer Sci Ther S2:004. doi: 10.4172/1948-5956.S2-004

Copyright: © 2011 Jones LP, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract

A major challenge to breast cancer research is the identification of alterations in the architecture and composition of the breast that are associated with breast cancer progression. The aim of the present investigation was to characterize the mammary adipose phenotype from Brca1 mutant mice in the expectation that this would shed light on the role of the mammary tissue environment in the early stages of breast tumorigenesis. We observed that histological sections of mammary tissue from adult Brca1 mutant mice abnormally display small, multilocular adipocytes that are reminiscent of brown adipose tissue (BAT) as compared to wildtype mice. Using a marker for BAT, the uncoupling protein 1 (UCP1), we demonstrated that these multilocular adipose regions in Brca1 mutant mice stain positive for UCP1. Transcriptionally, UCP1 mRNA levels in the Brca1 mutant mice were elevated greater than 50-fold compared to age-matched mammary glands from wildtype mice. Indeed, BAT has characteristics that are favorable for tumor growth, including high vascularity. Therefore, we also demonstrated that the multilocular brown adipose phenotype in the mammary fat pad of Brca1 mutant mice displayed regions of increased vascularity as evidenced by a significant increase in the protein expression of CD31, a marker for angiogenesis. This Brca1 mutant mouse model should provide a physiologically relevant context to determine whether brown adipose tissue can play a role in breast cancer development.

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