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Towards an integrated model for breast cancer etiology: The crucial role of the number of mammary tissue-specific stem cells

Perinatal events and conditions, notably birth weight, are associated with breast cancer risk in offspring, and correlates of mammary gland mass are predictors of breast cancer risk. These findings may be interpreted as indicating that high levels of estrogens and components of the insulin-like grow...

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Detalles Bibliográficos
Autores principales: Trichopoulos, Dimitrios, Lagiou, Pagona, Adami, Hans-Olov
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1064112/
https://www.ncbi.nlm.nih.gov/pubmed/15642176
http://dx.doi.org/10.1186/bcr966
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author Trichopoulos, Dimitrios
Lagiou, Pagona
Adami, Hans-Olov
author_facet Trichopoulos, Dimitrios
Lagiou, Pagona
Adami, Hans-Olov
author_sort Trichopoulos, Dimitrios
collection PubMed
description Perinatal events and conditions, notably birth weight, are associated with breast cancer risk in offspring, and correlates of mammary gland mass are predictors of breast cancer risk. These findings may be interpreted as indicating that high levels of estrogens and components of the insulin-like growth factor system during pregnancy favour the generation of mammary tissue-specific stem cells, and that the number of these cells, which is positively associated with mammary gland mass, is an important determinant of breast cancer risk. Perinatal events and conditions may also affect risk for other malignancies, but the evidence in the case of breast cancer is prominent, possibly because estrogens and the insulin-like growth factor system are both involved in breast cancer etiology and affect birth weight.
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spelling pubmed-10641122005-03-11 Towards an integrated model for breast cancer etiology: The crucial role of the number of mammary tissue-specific stem cells Trichopoulos, Dimitrios Lagiou, Pagona Adami, Hans-Olov Breast Cancer Res Review Perinatal events and conditions, notably birth weight, are associated with breast cancer risk in offspring, and correlates of mammary gland mass are predictors of breast cancer risk. These findings may be interpreted as indicating that high levels of estrogens and components of the insulin-like growth factor system during pregnancy favour the generation of mammary tissue-specific stem cells, and that the number of these cells, which is positively associated with mammary gland mass, is an important determinant of breast cancer risk. Perinatal events and conditions may also affect risk for other malignancies, but the evidence in the case of breast cancer is prominent, possibly because estrogens and the insulin-like growth factor system are both involved in breast cancer etiology and affect birth weight. BioMed Central 2005 2004-11-05 /pmc/articles/PMC1064112/ /pubmed/15642176 http://dx.doi.org/10.1186/bcr966 Text en Copyright © 2004 BioMed Central Ltd
spellingShingle Review
Trichopoulos, Dimitrios
Lagiou, Pagona
Adami, Hans-Olov
Towards an integrated model for breast cancer etiology: The crucial role of the number of mammary tissue-specific stem cells
title Towards an integrated model for breast cancer etiology: The crucial role of the number of mammary tissue-specific stem cells
title_full Towards an integrated model for breast cancer etiology: The crucial role of the number of mammary tissue-specific stem cells
title_fullStr Towards an integrated model for breast cancer etiology: The crucial role of the number of mammary tissue-specific stem cells
title_full_unstemmed Towards an integrated model for breast cancer etiology: The crucial role of the number of mammary tissue-specific stem cells
title_short Towards an integrated model for breast cancer etiology: The crucial role of the number of mammary tissue-specific stem cells
title_sort towards an integrated model for breast cancer etiology: the crucial role of the number of mammary tissue-specific stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1064112/
https://www.ncbi.nlm.nih.gov/pubmed/15642176
http://dx.doi.org/10.1186/bcr966
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