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High Intensity Interval Training Increases Natural Killer Cell Number and Function in Obese Breast Cancer-challenged Mice and Obese Women

High intensity interval training (HIIT) boosts natural killer (NK) cell number and activity in normal weight breast cancer patients; however, whether this occurs in obese individuals is not well established. The goal of this study was to determine whether HIIT effectively boosts NK cells as a therap...

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Autores principales: Barra, Nicole G., Fan, Isabella Y., Gillen, Jenna B., Chew, Marianne, Marcinko, Katarina, Steinberg, Gregory R., Gibala, Martin J., Ashkar, Ali A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Cancer Prevention 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751845/
https://www.ncbi.nlm.nih.gov/pubmed/29302585
http://dx.doi.org/10.15430/JCP.2017.22.4.260
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author Barra, Nicole G.
Fan, Isabella Y.
Gillen, Jenna B.
Chew, Marianne
Marcinko, Katarina
Steinberg, Gregory R.
Gibala, Martin J.
Ashkar, Ali A.
author_facet Barra, Nicole G.
Fan, Isabella Y.
Gillen, Jenna B.
Chew, Marianne
Marcinko, Katarina
Steinberg, Gregory R.
Gibala, Martin J.
Ashkar, Ali A.
author_sort Barra, Nicole G.
collection PubMed
description High intensity interval training (HIIT) boosts natural killer (NK) cell number and activity in normal weight breast cancer patients; however, whether this occurs in obese individuals is not well established. The goal of this study was to determine whether HIIT effectively boosts NK cells as a therapeutic strategy against breast cancer in an obese mouse model and in overweight/obese women. Diet induced female C57Bl/6 obese mice were assigned to undergo HIIT for four weeks or remain sedentary. Female participants were subjected to a six weeks HIIT protocol. HIIT mice acclimatized to treadmill running were subsequently injected with 5 × 10(5) polyoma middle T (MT) breast cancer cells intravenously. NK cell number and activation were monitored using flow cytometry, and tumor burden or lipid content evaluated from histological lung and liver tissues, respectively. In both mice and humans, circulating NK cell number and activation (CD3−NK1.1+CD27+ and CD3−CD56+, respectively) markedly increased immediately after HIIT. HIIT obese mice had reduced lung tumor burden compared to controls following MT challenge, and had diminished hepatic lipid deposition despite minimal body weight loss. Our findings demonstrate that HIIT can benefit obese individuals by enhancing NK cell number and activity, reducing tumor burden, and enhancing metabolic health.
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spelling pubmed-57518452018-01-04 High Intensity Interval Training Increases Natural Killer Cell Number and Function in Obese Breast Cancer-challenged Mice and Obese Women Barra, Nicole G. Fan, Isabella Y. Gillen, Jenna B. Chew, Marianne Marcinko, Katarina Steinberg, Gregory R. Gibala, Martin J. Ashkar, Ali A. J Cancer Prev Short Communication High intensity interval training (HIIT) boosts natural killer (NK) cell number and activity in normal weight breast cancer patients; however, whether this occurs in obese individuals is not well established. The goal of this study was to determine whether HIIT effectively boosts NK cells as a therapeutic strategy against breast cancer in an obese mouse model and in overweight/obese women. Diet induced female C57Bl/6 obese mice were assigned to undergo HIIT for four weeks or remain sedentary. Female participants were subjected to a six weeks HIIT protocol. HIIT mice acclimatized to treadmill running were subsequently injected with 5 × 10(5) polyoma middle T (MT) breast cancer cells intravenously. NK cell number and activation were monitored using flow cytometry, and tumor burden or lipid content evaluated from histological lung and liver tissues, respectively. In both mice and humans, circulating NK cell number and activation (CD3−NK1.1+CD27+ and CD3−CD56+, respectively) markedly increased immediately after HIIT. HIIT obese mice had reduced lung tumor burden compared to controls following MT challenge, and had diminished hepatic lipid deposition despite minimal body weight loss. Our findings demonstrate that HIIT can benefit obese individuals by enhancing NK cell number and activity, reducing tumor burden, and enhancing metabolic health. Korean Society of Cancer Prevention 2017-12 2017-12-30 /pmc/articles/PMC5751845/ /pubmed/29302585 http://dx.doi.org/10.15430/JCP.2017.22.4.260 Text en Copyright © 2017 Korean Society of Cancer Prevention This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Barra, Nicole G.
Fan, Isabella Y.
Gillen, Jenna B.
Chew, Marianne
Marcinko, Katarina
Steinberg, Gregory R.
Gibala, Martin J.
Ashkar, Ali A.
High Intensity Interval Training Increases Natural Killer Cell Number and Function in Obese Breast Cancer-challenged Mice and Obese Women
title High Intensity Interval Training Increases Natural Killer Cell Number and Function in Obese Breast Cancer-challenged Mice and Obese Women
title_full High Intensity Interval Training Increases Natural Killer Cell Number and Function in Obese Breast Cancer-challenged Mice and Obese Women
title_fullStr High Intensity Interval Training Increases Natural Killer Cell Number and Function in Obese Breast Cancer-challenged Mice and Obese Women
title_full_unstemmed High Intensity Interval Training Increases Natural Killer Cell Number and Function in Obese Breast Cancer-challenged Mice and Obese Women
title_short High Intensity Interval Training Increases Natural Killer Cell Number and Function in Obese Breast Cancer-challenged Mice and Obese Women
title_sort high intensity interval training increases natural killer cell number and function in obese breast cancer-challenged mice and obese women
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5751845/
https://www.ncbi.nlm.nih.gov/pubmed/29302585
http://dx.doi.org/10.15430/JCP.2017.22.4.260
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