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Breast cancer protection by genomic imprinting in close kin families

Human inbreeding generally reduces breast cancer risk (BCR). When the parents are biologically related, their infants have a lower birth weight due to smaller body organs. The undersized breasts, because of fewer mammary stem cells, have a lower likelihood of malignant conversion. Fetal growth is re...

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Detalles Bibliográficos
Autores principales: Denic, Srdjan, Agarwal, Mukesh M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696730/
https://www.ncbi.nlm.nih.gov/pubmed/29157216
http://dx.doi.org/10.1186/s12881-017-0498-0
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author Denic, Srdjan
Agarwal, Mukesh M.
author_facet Denic, Srdjan
Agarwal, Mukesh M.
author_sort Denic, Srdjan
collection PubMed
description Human inbreeding generally reduces breast cancer risk (BCR). When the parents are biologically related, their infants have a lower birth weight due to smaller body organs. The undersized breasts, because of fewer mammary stem cells, have a lower likelihood of malignant conversion. Fetal growth is regulated by genomically imprinted genes which are in conflict; they promote growth when derived from the father and suppress growth when derived from the mother. The kinship theory explicates that the intensity of conflict between these genes affects growth and therefore the size of the newborn. In descendants of closely related parents, this gene clash is less resulting in a smaller infant. In this review, we elucidate the different mechanisms by which human inbreeding affects BCR, and why this risk is dissimilar in different inbred populations.
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spelling pubmed-56967302017-12-01 Breast cancer protection by genomic imprinting in close kin families Denic, Srdjan Agarwal, Mukesh M. BMC Med Genet Review Human inbreeding generally reduces breast cancer risk (BCR). When the parents are biologically related, their infants have a lower birth weight due to smaller body organs. The undersized breasts, because of fewer mammary stem cells, have a lower likelihood of malignant conversion. Fetal growth is regulated by genomically imprinted genes which are in conflict; they promote growth when derived from the father and suppress growth when derived from the mother. The kinship theory explicates that the intensity of conflict between these genes affects growth and therefore the size of the newborn. In descendants of closely related parents, this gene clash is less resulting in a smaller infant. In this review, we elucidate the different mechanisms by which human inbreeding affects BCR, and why this risk is dissimilar in different inbred populations. BioMed Central 2017-11-21 /pmc/articles/PMC5696730/ /pubmed/29157216 http://dx.doi.org/10.1186/s12881-017-0498-0 Text en © The Author(s). 2017 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Denic, Srdjan
Agarwal, Mukesh M.
Breast cancer protection by genomic imprinting in close kin families
title Breast cancer protection by genomic imprinting in close kin families
title_full Breast cancer protection by genomic imprinting in close kin families
title_fullStr Breast cancer protection by genomic imprinting in close kin families
title_full_unstemmed Breast cancer protection by genomic imprinting in close kin families
title_short Breast cancer protection by genomic imprinting in close kin families
title_sort breast cancer protection by genomic imprinting in close kin families
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696730/
https://www.ncbi.nlm.nih.gov/pubmed/29157216
http://dx.doi.org/10.1186/s12881-017-0498-0
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