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Physical Activity Delays Obesity-Associated Pancreatic Ductal Adenocarcinoma in Mice and Decreases Inflammation
BACKGROUND & AIMS: Obesity is a risk factor for pancreatic ductal adenocarcinoma (PDAC), a deadly disease with limited preventive strategies. Lifestyle interventions to decrease obesity might prevent obesity-associated PDAC. Here, we examined whether decreasing obesity by increased physical acti...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881853/ https://www.ncbi.nlm.nih.gov/pubmed/36711764 http://dx.doi.org/10.1101/2023.01.03.521203 |
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author | Pita-Grisanti, Valentina Dubay, Kelly Lahooti, Ali Badi, Niharika Ueltschi, Olivia Gumpper-Fedus, Kristyn Hsueh, Hsiang-Yin Lahooti, Ila Chavez-Tomar, Myrriah Terhorst, Samantha Knoblaugh, Sue E. Cao, Lei Huang, Wei Coss, Christopher C. Mace, Thomas A. Choueiry, Fouad Hinton, Alice Mitchell, Jennifer M Schmandt, Rosemarie Grinsfelder, Michaela Onstad Basen-Engquist, Karen Cruz-Monserrate, Zobeida |
author_facet | Pita-Grisanti, Valentina Dubay, Kelly Lahooti, Ali Badi, Niharika Ueltschi, Olivia Gumpper-Fedus, Kristyn Hsueh, Hsiang-Yin Lahooti, Ila Chavez-Tomar, Myrriah Terhorst, Samantha Knoblaugh, Sue E. Cao, Lei Huang, Wei Coss, Christopher C. Mace, Thomas A. Choueiry, Fouad Hinton, Alice Mitchell, Jennifer M Schmandt, Rosemarie Grinsfelder, Michaela Onstad Basen-Engquist, Karen Cruz-Monserrate, Zobeida |
author_sort | Pita-Grisanti, Valentina |
collection | PubMed |
description | BACKGROUND & AIMS: Obesity is a risk factor for pancreatic ductal adenocarcinoma (PDAC), a deadly disease with limited preventive strategies. Lifestyle interventions to decrease obesity might prevent obesity-associated PDAC. Here, we examined whether decreasing obesity by increased physical activity (PA) and/or dietary changes would decrease inflammation in humans and prevent PDAC in mice. METHODS: Circulating inflammatory-associated cytokines of overweight and obese subjects before and after a PA intervention were compared. PDAC pre-clinical models were exposed to PA and/or dietary interventions after obesity-associated cancer initiation. Body composition, tumor progression, growth, fibrosis, inflammation, and transcriptomic changes in the adipose tissue were evaluated. RESULTS: PA decreased the levels of systemic inflammatory cytokines in overweight and obese subjects. PDAC mice on a diet-induced obesity (DIO) and PA intervention, had delayed weight gain, decreased systemic inflammation, lower grade pancreatic intraepithelial neoplasia lesions, reduced PDAC incidence, and increased anti-inflammatory signals in the adipose tissue compared to controls. PA had additional cancer prevention benefits when combined with a non-obesogenic diet after DIO. However, weight loss through PA alone or combined with a dietary intervention did not prevent tumor growth in an orthotopic PDAC model. Adipose-specific targeting of interleukin (IL)-15, an anti-inflammatory cytokine induced by PA in the adipose tissue, slowed PDAC growth. CONCLUSIONS: PA alone or combined with diet-induced weight loss delayed the progression of PDAC and reduced systemic and adipose inflammatory signals. Therefore, obesity management via dietary interventions and/or PA, or modulating weight loss related pathways could prevent obesity-associated PDAC in high-risk obese individuals. |
format | Online Article Text |
id | pubmed-9881853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-98818532023-01-28 Physical Activity Delays Obesity-Associated Pancreatic Ductal Adenocarcinoma in Mice and Decreases Inflammation Pita-Grisanti, Valentina Dubay, Kelly Lahooti, Ali Badi, Niharika Ueltschi, Olivia Gumpper-Fedus, Kristyn Hsueh, Hsiang-Yin Lahooti, Ila Chavez-Tomar, Myrriah Terhorst, Samantha Knoblaugh, Sue E. Cao, Lei Huang, Wei Coss, Christopher C. Mace, Thomas A. Choueiry, Fouad Hinton, Alice Mitchell, Jennifer M Schmandt, Rosemarie Grinsfelder, Michaela Onstad Basen-Engquist, Karen Cruz-Monserrate, Zobeida bioRxiv Article BACKGROUND & AIMS: Obesity is a risk factor for pancreatic ductal adenocarcinoma (PDAC), a deadly disease with limited preventive strategies. Lifestyle interventions to decrease obesity might prevent obesity-associated PDAC. Here, we examined whether decreasing obesity by increased physical activity (PA) and/or dietary changes would decrease inflammation in humans and prevent PDAC in mice. METHODS: Circulating inflammatory-associated cytokines of overweight and obese subjects before and after a PA intervention were compared. PDAC pre-clinical models were exposed to PA and/or dietary interventions after obesity-associated cancer initiation. Body composition, tumor progression, growth, fibrosis, inflammation, and transcriptomic changes in the adipose tissue were evaluated. RESULTS: PA decreased the levels of systemic inflammatory cytokines in overweight and obese subjects. PDAC mice on a diet-induced obesity (DIO) and PA intervention, had delayed weight gain, decreased systemic inflammation, lower grade pancreatic intraepithelial neoplasia lesions, reduced PDAC incidence, and increased anti-inflammatory signals in the adipose tissue compared to controls. PA had additional cancer prevention benefits when combined with a non-obesogenic diet after DIO. However, weight loss through PA alone or combined with a dietary intervention did not prevent tumor growth in an orthotopic PDAC model. Adipose-specific targeting of interleukin (IL)-15, an anti-inflammatory cytokine induced by PA in the adipose tissue, slowed PDAC growth. CONCLUSIONS: PA alone or combined with diet-induced weight loss delayed the progression of PDAC and reduced systemic and adipose inflammatory signals. Therefore, obesity management via dietary interventions and/or PA, or modulating weight loss related pathways could prevent obesity-associated PDAC in high-risk obese individuals. Cold Spring Harbor Laboratory 2023-01-04 /pmc/articles/PMC9881853/ /pubmed/36711764 http://dx.doi.org/10.1101/2023.01.03.521203 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Pita-Grisanti, Valentina Dubay, Kelly Lahooti, Ali Badi, Niharika Ueltschi, Olivia Gumpper-Fedus, Kristyn Hsueh, Hsiang-Yin Lahooti, Ila Chavez-Tomar, Myrriah Terhorst, Samantha Knoblaugh, Sue E. Cao, Lei Huang, Wei Coss, Christopher C. Mace, Thomas A. Choueiry, Fouad Hinton, Alice Mitchell, Jennifer M Schmandt, Rosemarie Grinsfelder, Michaela Onstad Basen-Engquist, Karen Cruz-Monserrate, Zobeida Physical Activity Delays Obesity-Associated Pancreatic Ductal Adenocarcinoma in Mice and Decreases Inflammation |
title | Physical Activity Delays Obesity-Associated Pancreatic Ductal Adenocarcinoma in Mice and Decreases Inflammation |
title_full | Physical Activity Delays Obesity-Associated Pancreatic Ductal Adenocarcinoma in Mice and Decreases Inflammation |
title_fullStr | Physical Activity Delays Obesity-Associated Pancreatic Ductal Adenocarcinoma in Mice and Decreases Inflammation |
title_full_unstemmed | Physical Activity Delays Obesity-Associated Pancreatic Ductal Adenocarcinoma in Mice and Decreases Inflammation |
title_short | Physical Activity Delays Obesity-Associated Pancreatic Ductal Adenocarcinoma in Mice and Decreases Inflammation |
title_sort | physical activity delays obesity-associated pancreatic ductal adenocarcinoma in mice and decreases inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9881853/ https://www.ncbi.nlm.nih.gov/pubmed/36711764 http://dx.doi.org/10.1101/2023.01.03.521203 |
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