Breast cancer and obesity: in vitro interferences between adipokines and proangiogenic features and/or antitumor therapies?

Obesity is now considered as a risk factor for breast cancer in postmenopausal women. Adipokine levels are modulated in obesity, and may play a role in carcinogenesis. Moreover, obesity increases risk of cancer mortality. Here, we hypothesized that this increase could be due to a modification in ang...

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Main Authors: Virginie Dubois, Laetitia Delort, Hermine Billard, Marie-Paule Vasson, Florence Caldefie-Chezet
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3598910?pdf=render
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spelling doaj-f87fd1d5b601431cba145f1b9feb5df22020-11-25T02:44:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5854110.1371/journal.pone.0058541Breast cancer and obesity: in vitro interferences between adipokines and proangiogenic features and/or antitumor therapies?Virginie DuboisLaetitia DelortHermine BillardMarie-Paule VassonFlorence Caldefie-ChezetObesity is now considered as a risk factor for breast cancer in postmenopausal women. Adipokine levels are modulated in obesity, and may play a role in carcinogenesis. Moreover, obesity increases risk of cancer mortality. Here, we hypothesized that this increase could be due to a modification in angiogenesis, capital event in the development of metastases, and/or in effectiveness of cancer treatments. To test these assumptions, following a same experimental design and simultaneously the effects of leptin and adiponectin on angiogenesis were investigated, and the impact of hyperleptinemia on anticancer drug effectiveness was measured in physiological and obesity situations. Focusing on angiogenesis, the proliferation of endothelial cells (HUVEC), which expressed leptin and adiponectin receptors, was stimulated by leptin and inhibited by adiponectin. Both adipokines globally reduced apoptosis and caspase activity. Leptin increased migration whereas adiponectin decreased migration, and leptin enhanced the area of the tubes formed by HUVEC cells while adiponectin inhibited their formation. MCF7 and MDA-MB-231 cells treated with leptin secreted more VEGF than untreated cells, whereas adiponectin treatment inhibited VEGF secretion. Finally, MCF7 cells pre-treated with leptin were more invasive than untreated cells. This effect was not reproduced in MDA-MB-231 cells. In the MCF7 breast cancer cell line, leptin could induce cell proliferation and reduced the efficacy of all breast cancer therapies (tamoxifen, 5-fluorouracil, taxol and vinblastin). These results suggest that, in obesity situation, leptin- in contrast to adiponectin - may promote tumor invasion and angiogenesis, leading to metastases 'apparition, and reduce treatment efficacy, which could explain the increased risk of cancer mortality in cases of overweight. The evidence suggests adipokines influence breast cancer issue and could play a significant role, especially in obese patients for which hyperleptinemia, hypoadiponectinemia and increased metastatic potential are described.http://europepmc.org/articles/PMC3598910?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Virginie Dubois
Laetitia Delort
Hermine Billard
Marie-Paule Vasson
Florence Caldefie-Chezet
spellingShingle Virginie Dubois
Laetitia Delort
Hermine Billard
Marie-Paule Vasson
Florence Caldefie-Chezet
Breast cancer and obesity: in vitro interferences between adipokines and proangiogenic features and/or antitumor therapies?
PLoS ONE
author_facet Virginie Dubois
Laetitia Delort
Hermine Billard
Marie-Paule Vasson
Florence Caldefie-Chezet
author_sort Virginie Dubois
title Breast cancer and obesity: in vitro interferences between adipokines and proangiogenic features and/or antitumor therapies?
title_short Breast cancer and obesity: in vitro interferences between adipokines and proangiogenic features and/or antitumor therapies?
title_full Breast cancer and obesity: in vitro interferences between adipokines and proangiogenic features and/or antitumor therapies?
title_fullStr Breast cancer and obesity: in vitro interferences between adipokines and proangiogenic features and/or antitumor therapies?
title_full_unstemmed Breast cancer and obesity: in vitro interferences between adipokines and proangiogenic features and/or antitumor therapies?
title_sort breast cancer and obesity: in vitro interferences between adipokines and proangiogenic features and/or antitumor therapies?
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Obesity is now considered as a risk factor for breast cancer in postmenopausal women. Adipokine levels are modulated in obesity, and may play a role in carcinogenesis. Moreover, obesity increases risk of cancer mortality. Here, we hypothesized that this increase could be due to a modification in angiogenesis, capital event in the development of metastases, and/or in effectiveness of cancer treatments. To test these assumptions, following a same experimental design and simultaneously the effects of leptin and adiponectin on angiogenesis were investigated, and the impact of hyperleptinemia on anticancer drug effectiveness was measured in physiological and obesity situations. Focusing on angiogenesis, the proliferation of endothelial cells (HUVEC), which expressed leptin and adiponectin receptors, was stimulated by leptin and inhibited by adiponectin. Both adipokines globally reduced apoptosis and caspase activity. Leptin increased migration whereas adiponectin decreased migration, and leptin enhanced the area of the tubes formed by HUVEC cells while adiponectin inhibited their formation. MCF7 and MDA-MB-231 cells treated with leptin secreted more VEGF than untreated cells, whereas adiponectin treatment inhibited VEGF secretion. Finally, MCF7 cells pre-treated with leptin were more invasive than untreated cells. This effect was not reproduced in MDA-MB-231 cells. In the MCF7 breast cancer cell line, leptin could induce cell proliferation and reduced the efficacy of all breast cancer therapies (tamoxifen, 5-fluorouracil, taxol and vinblastin). These results suggest that, in obesity situation, leptin- in contrast to adiponectin - may promote tumor invasion and angiogenesis, leading to metastases 'apparition, and reduce treatment efficacy, which could explain the increased risk of cancer mortality in cases of overweight. The evidence suggests adipokines influence breast cancer issue and could play a significant role, especially in obese patients for which hyperleptinemia, hypoadiponectinemia and increased metastatic potential are described.
url http://europepmc.org/articles/PMC3598910?pdf=render
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