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Tumor apelin and obesity are associated with reduced neoadjuvant chemotherapy response in a cohort of breast cancer patients
Obesity is a known factor increasing the risk of developing breast cancer and reducing disease free survival. In addition to these well-documented effects, recent studies have shown that obesity is also affecting response to chemotherapy. Among the multiple dysregulations associated with obesity, in...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110990/ https://www.ncbi.nlm.nih.gov/pubmed/33972642 http://dx.doi.org/10.1038/s41598-021-89385-z |
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author | Gourgue, Florian Derouane, Françoise van Marcke, Cedric Villar, Elodie Dano, Helene Desmet, Lieven Bouzin, Caroline Duhoux, Francois P. Cani, Patrice D. Jordan, Bénédicte F. |
author_facet | Gourgue, Florian Derouane, Françoise van Marcke, Cedric Villar, Elodie Dano, Helene Desmet, Lieven Bouzin, Caroline Duhoux, Francois P. Cani, Patrice D. Jordan, Bénédicte F. |
author_sort | Gourgue, Florian |
collection | PubMed |
description | Obesity is a known factor increasing the risk of developing breast cancer and reducing disease free survival. In addition to these well-documented effects, recent studies have shown that obesity is also affecting response to chemotherapy. Among the multiple dysregulations associated with obesity, increased level of the apelin adipokine has been recently shown to be directly involved in the association between obesity and increased breast cancer progression. In this study, we analyzed in a retrospective cohort of 62 breast cancer patients the impact of obesity and tumoral apelin expression on response to neoadjuvant chemotherapy. In the multivariate logistic regression, obesity and high tumoral apelin expression were associated with a reduced response to NAC in our cohort. However, obesity and high tumoral apelin expression were not correlated, suggesting that those two parameters could be independently associated with reduced NAC response. These findings should be confirmed in independent cohorts. |
format | Online Article Text |
id | pubmed-8110990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81109902021-05-12 Tumor apelin and obesity are associated with reduced neoadjuvant chemotherapy response in a cohort of breast cancer patients Gourgue, Florian Derouane, Françoise van Marcke, Cedric Villar, Elodie Dano, Helene Desmet, Lieven Bouzin, Caroline Duhoux, Francois P. Cani, Patrice D. Jordan, Bénédicte F. Sci Rep Article Obesity is a known factor increasing the risk of developing breast cancer and reducing disease free survival. In addition to these well-documented effects, recent studies have shown that obesity is also affecting response to chemotherapy. Among the multiple dysregulations associated with obesity, increased level of the apelin adipokine has been recently shown to be directly involved in the association between obesity and increased breast cancer progression. In this study, we analyzed in a retrospective cohort of 62 breast cancer patients the impact of obesity and tumoral apelin expression on response to neoadjuvant chemotherapy. In the multivariate logistic regression, obesity and high tumoral apelin expression were associated with a reduced response to NAC in our cohort. However, obesity and high tumoral apelin expression were not correlated, suggesting that those two parameters could be independently associated with reduced NAC response. These findings should be confirmed in independent cohorts. Nature Publishing Group UK 2021-05-10 /pmc/articles/PMC8110990/ /pubmed/33972642 http://dx.doi.org/10.1038/s41598-021-89385-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gourgue, Florian Derouane, Françoise van Marcke, Cedric Villar, Elodie Dano, Helene Desmet, Lieven Bouzin, Caroline Duhoux, Francois P. Cani, Patrice D. Jordan, Bénédicte F. Tumor apelin and obesity are associated with reduced neoadjuvant chemotherapy response in a cohort of breast cancer patients |
title | Tumor apelin and obesity are associated with reduced neoadjuvant chemotherapy response in a cohort of breast cancer patients |
title_full | Tumor apelin and obesity are associated with reduced neoadjuvant chemotherapy response in a cohort of breast cancer patients |
title_fullStr | Tumor apelin and obesity are associated with reduced neoadjuvant chemotherapy response in a cohort of breast cancer patients |
title_full_unstemmed | Tumor apelin and obesity are associated with reduced neoadjuvant chemotherapy response in a cohort of breast cancer patients |
title_short | Tumor apelin and obesity are associated with reduced neoadjuvant chemotherapy response in a cohort of breast cancer patients |
title_sort | tumor apelin and obesity are associated with reduced neoadjuvant chemotherapy response in a cohort of breast cancer patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110990/ https://www.ncbi.nlm.nih.gov/pubmed/33972642 http://dx.doi.org/10.1038/s41598-021-89385-z |
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