Cargando…

Charles River Sprague Dawley Rats Lack Early Age-Dependent Susceptibility to DMBA-Induced Mammary Carcinogenesis

Developmental stages of mammary glands influence their susceptibility to initiating events related to carcinogenesis. The “window of susceptibility” to mammary carcinogenesis is classically defined as the time in early puberty when the mammary gland morphology is most sensitive to initiation events....

Descripción completa

Detalles Bibliográficos
Autores principales: Gear, R.B., Yan, M., Schneider, J., Succop, P., Heffelfinger, S.C., Clegg, D.J.
Formato: Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2017109/
https://www.ncbi.nlm.nih.gov/pubmed/17940635
_version_ 1782136570836418560
author Gear, R.B.
Yan, M.
Schneider, J.
Succop, P.
Heffelfinger, S.C.
Clegg, D.J.
author_facet Gear, R.B.
Yan, M.
Schneider, J.
Succop, P.
Heffelfinger, S.C.
Clegg, D.J.
author_sort Gear, R.B.
collection PubMed
description Developmental stages of mammary glands influence their susceptibility to initiating events related to carcinogenesis. The “window of susceptibility” to mammary carcinogenesis is classically defined as the time in early puberty when the mammary gland morphology is most sensitive to initiation events. Administration of the polyaromatic hydrocarbon, 7,12-dimethylbenz(a)anthracene (DMBA), in a single oral dose yields maximal mammary tumor formation when administered in this “window”. We examined the DMBA treated mammary glands, precursor lesions, and morphology of the uninvolved mammary epithelium for the first 100 days of life for Charles River Sprague Dawley CD(R) IGS. Our goal was to determine the DMBA dose at which 50% of the rats (IC50) developed carcinoma in situ (CIS) within three months of dosing. Here we demonstrate, rather than the classical U-shaped dose curve in which there is maximum sensitivity for DMBA at 50 days, there is an increasing degree of sensitivity with age in the CD(R) IGS rat. Additionally, we report that vehicle-treated animals developed mammary CIS without any known initiator, and 100 day virgin animals demonstrated lactational changes, independent of DMBA exposure or dose. Lastly, we demonstrate this strain of virgin female rats has elevated pituitary prolactin immunoreactivity independent of the level of mammary differentiation. We conclude this strain of Charles River Sprague Dawley rats has prolactin-induced pituitary stimulation, and therefore, the window of susceptibility for mammary tumorigenesis is absent.
format Text
id pubmed-2017109
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-20171092007-10-16 Charles River Sprague Dawley Rats Lack Early Age-Dependent Susceptibility to DMBA-Induced Mammary Carcinogenesis Gear, R.B. Yan, M. Schneider, J. Succop, P. Heffelfinger, S.C. Clegg, D.J. Int J Biol Sci Research Paper Developmental stages of mammary glands influence their susceptibility to initiating events related to carcinogenesis. The “window of susceptibility” to mammary carcinogenesis is classically defined as the time in early puberty when the mammary gland morphology is most sensitive to initiation events. Administration of the polyaromatic hydrocarbon, 7,12-dimethylbenz(a)anthracene (DMBA), in a single oral dose yields maximal mammary tumor formation when administered in this “window”. We examined the DMBA treated mammary glands, precursor lesions, and morphology of the uninvolved mammary epithelium for the first 100 days of life for Charles River Sprague Dawley CD(R) IGS. Our goal was to determine the DMBA dose at which 50% of the rats (IC50) developed carcinoma in situ (CIS) within three months of dosing. Here we demonstrate, rather than the classical U-shaped dose curve in which there is maximum sensitivity for DMBA at 50 days, there is an increasing degree of sensitivity with age in the CD(R) IGS rat. Additionally, we report that vehicle-treated animals developed mammary CIS without any known initiator, and 100 day virgin animals demonstrated lactational changes, independent of DMBA exposure or dose. Lastly, we demonstrate this strain of virgin female rats has elevated pituitary prolactin immunoreactivity independent of the level of mammary differentiation. We conclude this strain of Charles River Sprague Dawley rats has prolactin-induced pituitary stimulation, and therefore, the window of susceptibility for mammary tumorigenesis is absent. Ivyspring International Publisher 2007-10-04 /pmc/articles/PMC2017109/ /pubmed/17940635 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Gear, R.B.
Yan, M.
Schneider, J.
Succop, P.
Heffelfinger, S.C.
Clegg, D.J.
Charles River Sprague Dawley Rats Lack Early Age-Dependent Susceptibility to DMBA-Induced Mammary Carcinogenesis
title Charles River Sprague Dawley Rats Lack Early Age-Dependent Susceptibility to DMBA-Induced Mammary Carcinogenesis
title_full Charles River Sprague Dawley Rats Lack Early Age-Dependent Susceptibility to DMBA-Induced Mammary Carcinogenesis
title_fullStr Charles River Sprague Dawley Rats Lack Early Age-Dependent Susceptibility to DMBA-Induced Mammary Carcinogenesis
title_full_unstemmed Charles River Sprague Dawley Rats Lack Early Age-Dependent Susceptibility to DMBA-Induced Mammary Carcinogenesis
title_short Charles River Sprague Dawley Rats Lack Early Age-Dependent Susceptibility to DMBA-Induced Mammary Carcinogenesis
title_sort charles river sprague dawley rats lack early age-dependent susceptibility to dmba-induced mammary carcinogenesis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2017109/
https://www.ncbi.nlm.nih.gov/pubmed/17940635
work_keys_str_mv AT gearrb charlesriverspraguedawleyratslackearlyagedependentsusceptibilitytodmbainducedmammarycarcinogenesis
AT yanm charlesriverspraguedawleyratslackearlyagedependentsusceptibilitytodmbainducedmammarycarcinogenesis
AT schneiderj charlesriverspraguedawleyratslackearlyagedependentsusceptibilitytodmbainducedmammarycarcinogenesis
AT succopp charlesriverspraguedawleyratslackearlyagedependentsusceptibilitytodmbainducedmammarycarcinogenesis
AT heffelfingersc charlesriverspraguedawleyratslackearlyagedependentsusceptibilitytodmbainducedmammarycarcinogenesis
AT cleggdj charlesriverspraguedawleyratslackearlyagedependentsusceptibilitytodmbainducedmammarycarcinogenesis