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Modeling Human Ductal Carcinoma In Situ in the Mouse

Breast cancer development is a multi-step process in which genetic and molecular heterogeneity occurs at multiple stages. Ductal carcinoma arises from pre-invasive lesions such as atypical ductal hyperplasia (ADH) and ductal carcinoma in situ (DCIS), which progress to invasive and metastatic cancer....

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Autores principales: Behbod, Fariba, Gomes, Angelica M., Machado, Heather L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244883/
https://www.ncbi.nlm.nih.gov/pubmed/30145750
http://dx.doi.org/10.1007/s10911-018-9408-0
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author Behbod, Fariba
Gomes, Angelica M.
Machado, Heather L.
author_facet Behbod, Fariba
Gomes, Angelica M.
Machado, Heather L.
author_sort Behbod, Fariba
collection PubMed
description Breast cancer development is a multi-step process in which genetic and molecular heterogeneity occurs at multiple stages. Ductal carcinoma arises from pre-invasive lesions such as atypical ductal hyperplasia (ADH) and ductal carcinoma in situ (DCIS), which progress to invasive and metastatic cancer. The feasibility of obtaining tissue samples from all stages of progression from the same patient is low, and thus molecular studies dissecting the mechanisms that mediate the transition from pre-invasive DCIS to invasive carcinoma have been hampered. In the past 25 years, numerous mouse models have been developed that partly recapitulate the histological and biological properties of early stage lesions. In this review, we discuss in vivo model systems of breast cancer progression from syngeneic mouse models to human xenografts, with particular focus on how accurately these models mimic human disease.
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spelling pubmed-62448832018-12-04 Modeling Human Ductal Carcinoma In Situ in the Mouse Behbod, Fariba Gomes, Angelica M. Machado, Heather L. J Mammary Gland Biol Neoplasia Article Breast cancer development is a multi-step process in which genetic and molecular heterogeneity occurs at multiple stages. Ductal carcinoma arises from pre-invasive lesions such as atypical ductal hyperplasia (ADH) and ductal carcinoma in situ (DCIS), which progress to invasive and metastatic cancer. The feasibility of obtaining tissue samples from all stages of progression from the same patient is low, and thus molecular studies dissecting the mechanisms that mediate the transition from pre-invasive DCIS to invasive carcinoma have been hampered. In the past 25 years, numerous mouse models have been developed that partly recapitulate the histological and biological properties of early stage lesions. In this review, we discuss in vivo model systems of breast cancer progression from syngeneic mouse models to human xenografts, with particular focus on how accurately these models mimic human disease. Springer US 2018-08-25 2018 /pmc/articles/PMC6244883/ /pubmed/30145750 http://dx.doi.org/10.1007/s10911-018-9408-0 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Behbod, Fariba
Gomes, Angelica M.
Machado, Heather L.
Modeling Human Ductal Carcinoma In Situ in the Mouse
title Modeling Human Ductal Carcinoma In Situ in the Mouse
title_full Modeling Human Ductal Carcinoma In Situ in the Mouse
title_fullStr Modeling Human Ductal Carcinoma In Situ in the Mouse
title_full_unstemmed Modeling Human Ductal Carcinoma In Situ in the Mouse
title_short Modeling Human Ductal Carcinoma In Situ in the Mouse
title_sort modeling human ductal carcinoma in situ in the mouse
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244883/
https://www.ncbi.nlm.nih.gov/pubmed/30145750
http://dx.doi.org/10.1007/s10911-018-9408-0
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