Kia Ranjbar1,2, Riccardo Ballarò1,3, Quim Bover1, Fabrizio Pin1,4, Marc Beltrà1,3, Fabio Penna1,3, Paola Costelli1,3. 1. Department of Clinical and Biological Sciences, University of Turin, Turin, ITALY. 2. Physical Education and Sport Sciences Department, Tarbiat Modares University, Teheran, IRAN. 3. Interuniversity Institute of Myology, Urbino, ITALY. 4. Department of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN.
Abstract
INTRODUCTION: Cancer cachexia is characterized by loss of muscle mass and function. Increased protein catabolism, inflammation, impaired anabolism, and mitochondrial function markedly contribute to the pathogenesis of this syndrome. Physical activity has been suggested as a useful tool to prevent or at least delay the onset and progression of cancer-induced muscle wasting. Two main types of exercise can be adopted, namely, resistance and endurance training. The present study is aimed to investigate the effectiveness of a combined (resistance + endurance) exercise protocol in preventing/reverting cancer-induced muscle wasting. METHODS: Mice bearing the C26 colon carcinoma have been used as a model of cancer cachexia. They have been exposed to combined exercise training during 6 wk (4 before tumor implantation, 2 during tumor growth). Climbing a 1-m ladder inclined at 85° has been used for resistance training, while aerobic (endurance) exercise has been carried out on the same day using a motorized wheel. RESULTS: In C26-bearing mice, both muscle mass and strength are improved by combined training, while just the latter increased in exercised healthy animals. Such a pattern is associated with modulations of two markers of autophagy, namely, LC3B-I/II ratio, increased in sedentary tumor hosts and reduced in exercised C26-bearing mice, and p62, steadily increased in both sedentary and trained tumor-bearing animals. Finally, combined training is not able to modify PGC-1α protein levels, but it improves succinate dehydrogenase activity, both reduced in the muscle of the C26 hosts. CONCLUSION: The data reported in the present study show that combined training improves muscle mass and function in the C26 hosts, likely modulating autophagy and improving mitochondrial function; these observations suggest that combined exercise might become part of a multimodal approach to treat cancer cachexia.
INTRODUCTION:Cancer cachexia is characterized by loss of muscle mass and function. Increased protein catabolism, inflammation, impaired anabolism, and mitochondrial function markedly contribute to the pathogenesis of this syndrome. Physical activity has been suggested as a useful tool to prevent or at least delay the onset and progression of cancer-induced muscle wasting. Two main types of exercise can be adopted, namely, resistance and endurance training. The present study is aimed to investigate the effectiveness of a combined (resistance + endurance) exercise protocol in preventing/reverting cancer-induced muscle wasting. METHODS:Mice bearing the C26 colon carcinoma have been used as a model of cancer cachexia. They have been exposed to combined exercise training during 6 wk (4 before tumor implantation, 2 during tumor growth). Climbing a 1-m ladder inclined at 85° has been used for resistance training, while aerobic (endurance) exercise has been carried out on the same day using a motorized wheel. RESULTS: In C26-bearing mice, both muscle mass and strength are improved by combined training, while just the latter increased in exercised healthy animals. Such a pattern is associated with modulations of two markers of autophagy, namely, LC3B-I/II ratio, increased in sedentary tumor hosts and reduced in exercised C26-bearing mice, and p62, steadily increased in both sedentary and trained tumor-bearing animals. Finally, combined training is not able to modify PGC-1α protein levels, but it improves succinate dehydrogenase activity, both reduced in the muscle of the C26 hosts. CONCLUSION: The data reported in the present study show that combined training improves muscle mass and function in the C26 hosts, likely modulating autophagy and improving mitochondrial function; these observations suggest that combined exercise might become part of a multimodal approach to treat cancer cachexia.
Authors: Mayra Tardelli de Jesus Testa; Paola Sanches Cella; Poliana Camila Marinello; Fernando Tadeu Trevisan Frajacomo; Camila de Souza Padilha; Patricia Chimin Perandini; Felipe Arruda Moura; José Alberto Duarte; Rubens Cecchini; Flavia Alessandra Guarnier; Rafael Deminice Journal: Front Oncol Date: 2022-07-01 Impact factor: 5.738
Authors: Andrea D Re Cecconi; Mara Forti; Michela Chiappa; Zhiyong Zhu; Leonid V Zingman; Luigi Cervo; Luca Beltrame; Sergio Marchini; Rosanna Piccirillo Journal: Cancers (Basel) Date: 2019-10-12 Impact factor: 6.639
Authors: Alisson L da Rocha; Ana P Pinto; Gustavo P Morais; Bruno B Marafon; Rafael L Rovina; Allice S C Veras; Giovana R Teixeira; José R Pauli; Leandro P de Moura; Dennys E Cintra; Eduardo R Ropelle; Donato A Rivas; Adelino S R da Silva Journal: Int J Mol Sci Date: 2020-11-10 Impact factor: 5.923
Authors: Giorgio Aquila; Andrea David Re Cecconi; Jeffrey J Brault; Oscar Corli; Rosanna Piccirillo Journal: Cells Date: 2020-11-24 Impact factor: 6.600
Authors: Ana P Pinto; Alisson L da Rocha; Bruno B Marafon; Rafael L Rovina; Vitor R Muñoz; Lilian E C M da Silva; José R Pauli; Leandro P de Moura; Dennys E Cintra; Eduardo R Ropelle; Adelino S R da Silva Journal: Int J Mol Sci Date: 2021-03-05 Impact factor: 5.923
Authors: Daniel Garrigos; Marta Martínez-Morga; Angel Toval; Yevheniy Kutsenko; Alberto Barreda; Bruno Ribeiro Do Couto; Fernando Navarro-Mateu; José Luis Ferran Journal: Front Endocrinol (Lausanne) Date: 2021-05-10 Impact factor: 5.555