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Expression of estrogen receptor, progesterone receptor, and Ki67 in normal breast tissue in relation to subsequent risk of breast cancer
Although expression of estrogen receptor (ER), progesterone receptor (PR), and cell proliferation marker Ki67 serve as predictive and prognostic factors in breast cancers, little is known about their roles in normal breast tissue. Here in a nested case–control study within the Nurses’ Health Studies...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243126/ https://www.ncbi.nlm.nih.gov/pubmed/28111631 http://dx.doi.org/10.1038/npjbcancer.2016.32 |
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author | Oh, Hannah Eliassen, A Heather Wang, Molin Smith-Warner, Stephanie A Beck, Andrew H Schnitt, Stuart J Collins, Laura C Connolly, James L Montaser-Kouhsari, Laleh Polyak, Kornelia Tamimi, Rulla M |
author_facet | Oh, Hannah Eliassen, A Heather Wang, Molin Smith-Warner, Stephanie A Beck, Andrew H Schnitt, Stuart J Collins, Laura C Connolly, James L Montaser-Kouhsari, Laleh Polyak, Kornelia Tamimi, Rulla M |
author_sort | Oh, Hannah |
collection | PubMed |
description | Although expression of estrogen receptor (ER), progesterone receptor (PR), and cell proliferation marker Ki67 serve as predictive and prognostic factors in breast cancers, little is known about their roles in normal breast tissue. Here in a nested case–control study within the Nurses’ Health Studies (90 cases, 297 controls), we evaluated their expression levels in normal breast epithelium in relation to subsequent breast cancer risk among women with benign breast disease. Tissue microarrays were constructed using cores obtained from benign biopsies containing normal terminal duct lobular units and immunohistochemical stained for these markers. We found PR and Ki67 expression was non-significantly but positively associated with subsequent breast cancer risk, whereas ER expression was non-significantly inversely associated. After stratifying by lesion subtype, Ki67 was significantly associated with higher risk among women with proliferative lesions with atypical hyperplasia. However, given the small sample size, further studies are required to confirm these results. |
format | Online Article Text |
id | pubmed-5243126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52431262017-01-18 Expression of estrogen receptor, progesterone receptor, and Ki67 in normal breast tissue in relation to subsequent risk of breast cancer Oh, Hannah Eliassen, A Heather Wang, Molin Smith-Warner, Stephanie A Beck, Andrew H Schnitt, Stuart J Collins, Laura C Connolly, James L Montaser-Kouhsari, Laleh Polyak, Kornelia Tamimi, Rulla M NPJ Breast Cancer Brief Communication Although expression of estrogen receptor (ER), progesterone receptor (PR), and cell proliferation marker Ki67 serve as predictive and prognostic factors in breast cancers, little is known about their roles in normal breast tissue. Here in a nested case–control study within the Nurses’ Health Studies (90 cases, 297 controls), we evaluated their expression levels in normal breast epithelium in relation to subsequent breast cancer risk among women with benign breast disease. Tissue microarrays were constructed using cores obtained from benign biopsies containing normal terminal duct lobular units and immunohistochemical stained for these markers. We found PR and Ki67 expression was non-significantly but positively associated with subsequent breast cancer risk, whereas ER expression was non-significantly inversely associated. After stratifying by lesion subtype, Ki67 was significantly associated with higher risk among women with proliferative lesions with atypical hyperplasia. However, given the small sample size, further studies are required to confirm these results. Nature Publishing Group 2016-10-26 /pmc/articles/PMC5243126/ /pubmed/28111631 http://dx.doi.org/10.1038/npjbcancer.2016.32 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Brief Communication Oh, Hannah Eliassen, A Heather Wang, Molin Smith-Warner, Stephanie A Beck, Andrew H Schnitt, Stuart J Collins, Laura C Connolly, James L Montaser-Kouhsari, Laleh Polyak, Kornelia Tamimi, Rulla M Expression of estrogen receptor, progesterone receptor, and Ki67 in normal breast tissue in relation to subsequent risk of breast cancer |
title | Expression of estrogen receptor, progesterone receptor, and Ki67 in normal breast tissue in relation to subsequent risk of breast cancer |
title_full | Expression of estrogen receptor, progesterone receptor, and Ki67 in normal breast tissue in relation to subsequent risk of breast cancer |
title_fullStr | Expression of estrogen receptor, progesterone receptor, and Ki67 in normal breast tissue in relation to subsequent risk of breast cancer |
title_full_unstemmed | Expression of estrogen receptor, progesterone receptor, and Ki67 in normal breast tissue in relation to subsequent risk of breast cancer |
title_short | Expression of estrogen receptor, progesterone receptor, and Ki67 in normal breast tissue in relation to subsequent risk of breast cancer |
title_sort | expression of estrogen receptor, progesterone receptor, and ki67 in normal breast tissue in relation to subsequent risk of breast cancer |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243126/ https://www.ncbi.nlm.nih.gov/pubmed/28111631 http://dx.doi.org/10.1038/npjbcancer.2016.32 |
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