Spontaneous Physical Activity Downregulates Pax7 in Cancer Cachexia

Emerging evidence suggests that the muscle microenvironment plays a prominent role in cancer cachexia. We recently showed that NF-kB-induced Pax7 overexpression impairs the myogenic potential of muscle precursors in cachectic mice, suggesting that lowering Pax7 expression may be beneficial in cancer...

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Main Authors: Dario Coletti, Paola Aulino, Eva Pigna, Fabio Barteri, Viviana Moresi, Daniela Annibali, Sergio Adamo, Emanuele Berardi
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2016/6729268
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author Dario Coletti
Paola Aulino
Eva Pigna
Fabio Barteri
Viviana Moresi
Daniela Annibali
Sergio Adamo
Emanuele Berardi
author_facet Dario Coletti
Paola Aulino
Eva Pigna
Fabio Barteri
Viviana Moresi
Daniela Annibali
Sergio Adamo
Emanuele Berardi
author_sort Dario Coletti
collection DOAJ
description Emerging evidence suggests that the muscle microenvironment plays a prominent role in cancer cachexia. We recently showed that NF-kB-induced Pax7 overexpression impairs the myogenic potential of muscle precursors in cachectic mice, suggesting that lowering Pax7 expression may be beneficial in cancer cachexia. We evaluated the muscle regenerative potential after acute injury in C26 colon carcinoma tumor-bearing mice and healthy controls. Our analyses confirmed that the delayed muscle regeneration observed in muscles form tumor-bearing mice was associated with a persistent local inflammation and Pax7 overexpression. Physical activity is known to exert positive effects on cachectic muscles. However, the mechanism by which a moderate voluntary exercise ameliorates muscle wasting is not fully elucidated. To verify if physical activity affects Pax7 expression, we hosted control and C26-bearing mice in wheel-equipped cages and we found that voluntary wheel running downregulated Pax7 expression in muscles from tumor-bearing mice. As expected, downregulation of Pax7 expression was associated with a rescue of muscle mass and fiber size. Our findings shed light on the molecular basis of the beneficial effect exerted by a moderate physical exercise on muscle stem cells in cancer cachexia. Furthermore, we propose voluntary exercise as a physiological tool to counteract the overexpression of Pax7 observed in cancer cachexia.
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spelling doaj-art-2bf106a6068a4ffeaf078aabea6515502025-02-03T01:25:57ZengWileyStem Cells International1687-966X1687-96782016-01-01201610.1155/2016/67292686729268Spontaneous Physical Activity Downregulates Pax7 in Cancer CachexiaDario Coletti0Paola Aulino1Eva Pigna2Fabio Barteri3Viviana Moresi4Daniela Annibali5Sergio Adamo6Emanuele Berardi7DAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Via Scarpa 14, 00161 Rome, ItalyDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Via Scarpa 14, 00161 Rome, ItalyDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Via Scarpa 14, 00161 Rome, ItalyDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Via Scarpa 14, 00161 Rome, ItalyDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Via Scarpa 14, 00161 Rome, ItalyBiology, Molecular Medicine and Nano-Biotechnologies Institute, C.N.R., Biology and Biotechnologies Department, Sapienza University of Rome, 00185 Rome, ItalyDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Via Scarpa 14, 00161 Rome, ItalyDAHFMO Unit of Histology and Medical Embryology, Interuniversity Institute of Myology, Sapienza University of Rome, Via Scarpa 14, 00161 Rome, ItalyEmerging evidence suggests that the muscle microenvironment plays a prominent role in cancer cachexia. We recently showed that NF-kB-induced Pax7 overexpression impairs the myogenic potential of muscle precursors in cachectic mice, suggesting that lowering Pax7 expression may be beneficial in cancer cachexia. We evaluated the muscle regenerative potential after acute injury in C26 colon carcinoma tumor-bearing mice and healthy controls. Our analyses confirmed that the delayed muscle regeneration observed in muscles form tumor-bearing mice was associated with a persistent local inflammation and Pax7 overexpression. Physical activity is known to exert positive effects on cachectic muscles. However, the mechanism by which a moderate voluntary exercise ameliorates muscle wasting is not fully elucidated. To verify if physical activity affects Pax7 expression, we hosted control and C26-bearing mice in wheel-equipped cages and we found that voluntary wheel running downregulated Pax7 expression in muscles from tumor-bearing mice. As expected, downregulation of Pax7 expression was associated with a rescue of muscle mass and fiber size. Our findings shed light on the molecular basis of the beneficial effect exerted by a moderate physical exercise on muscle stem cells in cancer cachexia. Furthermore, we propose voluntary exercise as a physiological tool to counteract the overexpression of Pax7 observed in cancer cachexia.http://dx.doi.org/10.1155/2016/6729268
spellingShingle Dario Coletti
Paola Aulino
Eva Pigna
Fabio Barteri
Viviana Moresi
Daniela Annibali
Sergio Adamo
Emanuele Berardi
Spontaneous Physical Activity Downregulates Pax7 in Cancer Cachexia
Stem Cells International
title Spontaneous Physical Activity Downregulates Pax7 in Cancer Cachexia
title_full Spontaneous Physical Activity Downregulates Pax7 in Cancer Cachexia
title_fullStr Spontaneous Physical Activity Downregulates Pax7 in Cancer Cachexia
title_full_unstemmed Spontaneous Physical Activity Downregulates Pax7 in Cancer Cachexia
title_short Spontaneous Physical Activity Downregulates Pax7 in Cancer Cachexia
title_sort spontaneous physical activity downregulates pax7 in cancer cachexia
url http://dx.doi.org/10.1155/2016/6729268
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AT vivianamoresi spontaneousphysicalactivitydownregulatespax7incancercachexia
AT danielaannibali spontaneousphysicalactivitydownregulatespax7incancercachexia
AT sergioadamo spontaneousphysicalactivitydownregulatespax7incancercachexia
AT emanueleberardi spontaneousphysicalactivitydownregulatespax7incancercachexia