CEBP Infection and Cancer: Biology, Therapeutics, and Prevention Translational Cancer Medicine 2008: Cancer Clinical Trials and Personalized Medicine
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Cancer Epidemiology Biomarkers & Prevention 16, 2247-2256, November 1, 2007. Published Online First November 2, 2007;
doi: 10.1158/1055-9965.EPI-06-0932
© 2007 American Association for Cancer Research

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Spontaneous Mammary Intraepithelial Lesions in Dogs—A Model of Breast Cancer

Elisabetta Antuofermo1, Margaret A. Miller1, Salvatore Pirino4, Jun Xie2, Sunil Badve5 and Sulma I. Mohammed1,3

Departments of 1 Comparative Pathobiology and 2 Statistics and 3 Purdue University Cancer Center, Purdue University, West Lafayette, Indiana; 4 Institute of General and Anatomical Pathology, Sassari University School of Veterinary Medicine, Sardinia, Italy; and 5 Department of Pathology, Indiana University School of Medicine, Indianapolis, Indiana

Requests for reprints: Sulma I. Mohammed, Department of Veterinary Pathobiology, Purdue University, West Lafayette, IN 47907. Phone: 765-494-9948; Fax: 765-494-9830. E-mail: mohammes{at}purdue.edu

Mammary intraepithelial lesions (IEL) are nowadays frequently diagnosed as a result of the success of mammographic screening, education programs, and awareness by women. Establishment of an animal model for these lesions to test treatment or preventive modalities is a prerequisite for human clinical trials. A model for spontaneous IELs, especially for estrogen receptor (ER)-negative lesions, does not exist. This study describes the histologic and immunohistochemical similarity between human and canine mammary IELs. Mammary tumors from 200 dogs were classified and histologic sections of the excisional specimens were evaluated for IELs. IELs, found in specimens from 60 dogs, were categorized as adenosis, sclerosing adenosis, intraductal papilloma, sclerosing papilloma, ductal hyperplasia, atypical ductal hyperplasia (ADH), and ductal carcinoma in situ (DCIS; high, intermediate, and low grade). Most proliferative IELs without atypia were associated with benign tumors, whereas IELs with atypia (ADH and DCIS) were generally associated with mammary cancer. ER-{alpha} expression was significantly low or absent in most ADH and DCIS lesions as well as in their associated tumors. Ki67 expression was significantly higher in high-grade DCIS than in hyperplasia or low-grade DCIS. Two thirds of high-grade DCIS lesions were positive for HER-2. Canine mammary IELs were strikingly similar to those of the human breast. The frequency of IELs in the dog, their association with spontaneous mammary cancer, their pattern of ER-{alpha} and HER-2 expression, and their histologic resemblance to human IELs may make the dog an ideal model to study human ER-negative (both HER-2 positive and negative) breast cancer progression as well as prevention and treatment. (Cancer Epidemiol Biomarkers Prev 2007;16(11):2247–56)


Commentary

Canine Genetics Offers New Mechanisms for the Study of Human Cancer
Edouard Cadieu and Elaine A. Ostrander
Cancer Epidemiol. Biomarkers Prev. 2007 16: 2181-2183. [Full Text] [PDF]



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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Cell Growth & Differentiation
Copyright © 2007 by the American Association for Cancer Research.