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Inflammatory Biomarkers and Breast Cancer Risk: A Systematic Review of the Evidence and Future Potential for Intervention Research

Measuring systemic chronic inflammatory markers in the blood may be one way of understanding the role of inflammation in breast cancer risk, and might provide an intermediate outcome marker in prevention studies. Here, we present the results of a systematic review of prospective epidemiologic studie...

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Autores principales: Kehm, Rebecca D., McDonald, Jasmine A., Fenton, Suzanne E., Kavanaugh-Lynch, Marion, Leung, Karling Alice, McKenzie, Katherine E., Mandelblatt, Jeanne S., Terry, Mary Beth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432395/
https://www.ncbi.nlm.nih.gov/pubmed/32731638
http://dx.doi.org/10.3390/ijerph17155445
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author Kehm, Rebecca D.
McDonald, Jasmine A.
Fenton, Suzanne E.
Kavanaugh-Lynch, Marion
Leung, Karling Alice
McKenzie, Katherine E.
Mandelblatt, Jeanne S.
Terry, Mary Beth
author_facet Kehm, Rebecca D.
McDonald, Jasmine A.
Fenton, Suzanne E.
Kavanaugh-Lynch, Marion
Leung, Karling Alice
McKenzie, Katherine E.
Mandelblatt, Jeanne S.
Terry, Mary Beth
author_sort Kehm, Rebecca D.
collection PubMed
description Measuring systemic chronic inflammatory markers in the blood may be one way of understanding the role of inflammation in breast cancer risk, and might provide an intermediate outcome marker in prevention studies. Here, we present the results of a systematic review of prospective epidemiologic studies that examined associations between systemic inflammatory biomarkers measured in blood and breast cancer risk. From 1 January 2014 to 20 April 2020, we identified 18 unique studies (from 16 publications) that examined the association of systemic inflammatory biomarkers measured in blood with breast cancer risk using prospectively collected epidemiologic data. Only one marker, C-reactive protein, was studied extensively (measured in 13 of the 16 publications), and had some evidence of a positive association with breast cancer risk. Evidence associating other inflammatory biomarkers and more comprehensive panels of markers with the development of breast cancer is limited. Future prospective evidence from expanded panels of systemic blood inflammatory biomarkers is needed to establish strong and independent links with breast cancer risk, along with mechanistic studies to understand inflammatory pathways and demonstrate how breast tissue responds to chronic inflammation. This knowledge could ultimately support the development and evaluation of mechanistically driven interventions to reduce inflammation and prevent breast cancer.
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spelling pubmed-74323952020-08-24 Inflammatory Biomarkers and Breast Cancer Risk: A Systematic Review of the Evidence and Future Potential for Intervention Research Kehm, Rebecca D. McDonald, Jasmine A. Fenton, Suzanne E. Kavanaugh-Lynch, Marion Leung, Karling Alice McKenzie, Katherine E. Mandelblatt, Jeanne S. Terry, Mary Beth Int J Environ Res Public Health Review Measuring systemic chronic inflammatory markers in the blood may be one way of understanding the role of inflammation in breast cancer risk, and might provide an intermediate outcome marker in prevention studies. Here, we present the results of a systematic review of prospective epidemiologic studies that examined associations between systemic inflammatory biomarkers measured in blood and breast cancer risk. From 1 January 2014 to 20 April 2020, we identified 18 unique studies (from 16 publications) that examined the association of systemic inflammatory biomarkers measured in blood with breast cancer risk using prospectively collected epidemiologic data. Only one marker, C-reactive protein, was studied extensively (measured in 13 of the 16 publications), and had some evidence of a positive association with breast cancer risk. Evidence associating other inflammatory biomarkers and more comprehensive panels of markers with the development of breast cancer is limited. Future prospective evidence from expanded panels of systemic blood inflammatory biomarkers is needed to establish strong and independent links with breast cancer risk, along with mechanistic studies to understand inflammatory pathways and demonstrate how breast tissue responds to chronic inflammation. This knowledge could ultimately support the development and evaluation of mechanistically driven interventions to reduce inflammation and prevent breast cancer. MDPI 2020-07-28 2020-08 /pmc/articles/PMC7432395/ /pubmed/32731638 http://dx.doi.org/10.3390/ijerph17155445 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Kehm, Rebecca D.
McDonald, Jasmine A.
Fenton, Suzanne E.
Kavanaugh-Lynch, Marion
Leung, Karling Alice
McKenzie, Katherine E.
Mandelblatt, Jeanne S.
Terry, Mary Beth
Inflammatory Biomarkers and Breast Cancer Risk: A Systematic Review of the Evidence and Future Potential for Intervention Research
title Inflammatory Biomarkers and Breast Cancer Risk: A Systematic Review of the Evidence and Future Potential for Intervention Research
title_full Inflammatory Biomarkers and Breast Cancer Risk: A Systematic Review of the Evidence and Future Potential for Intervention Research
title_fullStr Inflammatory Biomarkers and Breast Cancer Risk: A Systematic Review of the Evidence and Future Potential for Intervention Research
title_full_unstemmed Inflammatory Biomarkers and Breast Cancer Risk: A Systematic Review of the Evidence and Future Potential for Intervention Research
title_short Inflammatory Biomarkers and Breast Cancer Risk: A Systematic Review of the Evidence and Future Potential for Intervention Research
title_sort inflammatory biomarkers and breast cancer risk: a systematic review of the evidence and future potential for intervention research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432395/
https://www.ncbi.nlm.nih.gov/pubmed/32731638
http://dx.doi.org/10.3390/ijerph17155445
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