TGF-β Blockade Reduces Mortality and Metabolic Changes in a Validated Murine Model of Pancreatic Cancer Cachexia.

Cancer cachexia is a debilitating condition characterized by a combination of anorexia, muscle wasting, weight loss, and malnutrition. This condition affects an overwhelming majority of patients with pancreatic cancer and is a primary cause of cancer-related death. However, few, if any, effective th...

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Main Authors: Stephanie H Greco, Lena Tomkötter, Anne-Kristin Vahle, Rae Rokosh, Antonina Avanzi, Syed Kashif Mahmood, Michael Deutsch, Sara Alothman, Dalia Alqunaibit, Atsuo Ochi, Constantinos Zambirinis, Tasnima Mohaimin, Mauricio Rendon, Elliot Levie, Mridul Pansari, Alejandro Torres-Hernandez, Donnele Daley, Rocky Barilla, H Leon Pachter, Daniel Tippens, Hassan Malik, Allal Boutajangout, Thomas Wisniewski, George Miller
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0132786
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author Stephanie H Greco
Lena Tomkötter
Anne-Kristin Vahle
Rae Rokosh
Antonina Avanzi
Syed Kashif Mahmood
Michael Deutsch
Sara Alothman
Dalia Alqunaibit
Atsuo Ochi
Constantinos Zambirinis
Tasnima Mohaimin
Mauricio Rendon
Elliot Levie
Mridul Pansari
Alejandro Torres-Hernandez
Donnele Daley
Rocky Barilla
H Leon Pachter
Daniel Tippens
Hassan Malik
Allal Boutajangout
Thomas Wisniewski
George Miller
author_facet Stephanie H Greco
Lena Tomkötter
Anne-Kristin Vahle
Rae Rokosh
Antonina Avanzi
Syed Kashif Mahmood
Michael Deutsch
Sara Alothman
Dalia Alqunaibit
Atsuo Ochi
Constantinos Zambirinis
Tasnima Mohaimin
Mauricio Rendon
Elliot Levie
Mridul Pansari
Alejandro Torres-Hernandez
Donnele Daley
Rocky Barilla
H Leon Pachter
Daniel Tippens
Hassan Malik
Allal Boutajangout
Thomas Wisniewski
George Miller
author_sort Stephanie H Greco
collection DOAJ
description Cancer cachexia is a debilitating condition characterized by a combination of anorexia, muscle wasting, weight loss, and malnutrition. This condition affects an overwhelming majority of patients with pancreatic cancer and is a primary cause of cancer-related death. However, few, if any, effective therapies exist for both treatment and prevention of this syndrome. In order to develop novel therapeutic strategies for pancreatic cancer cachexia, appropriate animal models are necessary. In this study, we developed and validated a syngeneic, metastatic, murine model of pancreatic cancer cachexia. Using our model, we investigated the ability of transforming growth factor beta (TGF-β) blockade to mitigate the metabolic changes associated with cachexia. We found that TGF-β inhibition using the anti-TGF-β antibody 1D11.16.8 significantly improved overall mortality, weight loss, fat mass, lean body mass, bone mineral density, and skeletal muscle proteolysis in mice harboring advanced pancreatic cancer. Other immunotherapeutic strategies we employed were not effective. Collectively, we validated a simplified but useful model of pancreatic cancer cachexia to investigate immunologic treatment strategies. In addition, we showed that TGF-β inhibition can decrease the metabolic changes associated with cancer cachexia and improve overall survival.
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spelling doaj.art-b7fd88cea2a54aa2a12d6e6bd5e2ee5f2024-01-18T06:15:11ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01107e013278610.1371/journal.pone.0132786TGF-β Blockade Reduces Mortality and Metabolic Changes in a Validated Murine Model of Pancreatic Cancer Cachexia.Stephanie H GrecoLena TomkötterAnne-Kristin VahleRae RokoshAntonina AvanziSyed Kashif MahmoodMichael DeutschSara AlothmanDalia AlqunaibitAtsuo OchiConstantinos ZambirinisTasnima MohaiminMauricio RendonElliot LevieMridul PansariAlejandro Torres-HernandezDonnele DaleyRocky BarillaH Leon PachterDaniel TippensHassan MalikAllal BoutajangoutThomas WisniewskiGeorge MillerCancer cachexia is a debilitating condition characterized by a combination of anorexia, muscle wasting, weight loss, and malnutrition. This condition affects an overwhelming majority of patients with pancreatic cancer and is a primary cause of cancer-related death. However, few, if any, effective therapies exist for both treatment and prevention of this syndrome. In order to develop novel therapeutic strategies for pancreatic cancer cachexia, appropriate animal models are necessary. In this study, we developed and validated a syngeneic, metastatic, murine model of pancreatic cancer cachexia. Using our model, we investigated the ability of transforming growth factor beta (TGF-β) blockade to mitigate the metabolic changes associated with cachexia. We found that TGF-β inhibition using the anti-TGF-β antibody 1D11.16.8 significantly improved overall mortality, weight loss, fat mass, lean body mass, bone mineral density, and skeletal muscle proteolysis in mice harboring advanced pancreatic cancer. Other immunotherapeutic strategies we employed were not effective. Collectively, we validated a simplified but useful model of pancreatic cancer cachexia to investigate immunologic treatment strategies. In addition, we showed that TGF-β inhibition can decrease the metabolic changes associated with cancer cachexia and improve overall survival.https://doi.org/10.1371/journal.pone.0132786
spellingShingle Stephanie H Greco
Lena Tomkötter
Anne-Kristin Vahle
Rae Rokosh
Antonina Avanzi
Syed Kashif Mahmood
Michael Deutsch
Sara Alothman
Dalia Alqunaibit
Atsuo Ochi
Constantinos Zambirinis
Tasnima Mohaimin
Mauricio Rendon
Elliot Levie
Mridul Pansari
Alejandro Torres-Hernandez
Donnele Daley
Rocky Barilla
H Leon Pachter
Daniel Tippens
Hassan Malik
Allal Boutajangout
Thomas Wisniewski
George Miller
TGF-β Blockade Reduces Mortality and Metabolic Changes in a Validated Murine Model of Pancreatic Cancer Cachexia.
PLoS ONE
title TGF-β Blockade Reduces Mortality and Metabolic Changes in a Validated Murine Model of Pancreatic Cancer Cachexia.
title_full TGF-β Blockade Reduces Mortality and Metabolic Changes in a Validated Murine Model of Pancreatic Cancer Cachexia.
title_fullStr TGF-β Blockade Reduces Mortality and Metabolic Changes in a Validated Murine Model of Pancreatic Cancer Cachexia.
title_full_unstemmed TGF-β Blockade Reduces Mortality and Metabolic Changes in a Validated Murine Model of Pancreatic Cancer Cachexia.
title_short TGF-β Blockade Reduces Mortality and Metabolic Changes in a Validated Murine Model of Pancreatic Cancer Cachexia.
title_sort tgf β blockade reduces mortality and metabolic changes in a validated murine model of pancreatic cancer cachexia
url https://doi.org/10.1371/journal.pone.0132786
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