Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/33216
Title: Spontaneous Physical Activity Downregulates Pax7 in Cancer Cachexia
Authors: Coletti, D
Aulino, P
Pigna, E
Barteri, F
Moresi, V
Annibali, D
Adamo, S
BERARDI, Emanuele 
Issue Date: 2015
Publisher: HINDAWI LTD
Source: Stem Cells International, 2016 (Art N° 6729268)
Abstract: 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.
Document URI: http://hdl.handle.net/1942/33216
Link to publication/dataset: http://europepmc.org/articles/PMC4807049
ISSN: 1687-966X
e-ISSN: 1687-9678
DOI: 10.1155/2016/6729268
ISI #: WOS:000369721800001
Rights: 2016 Dario Coletti et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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