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      The effect of strength training on muscle cellular stress in prostate cancer patients on ADT

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          Abstract

          Background

          Androgen deprivation therapy (ADT) for prostate cancer (PCa) is associated with several side effects, including loss of muscle mass. Muscle atrophy is associated with reduced mitochondrial function and increased muscle cellular stress that may be counteracted by strength training. Thus, the aim of this study was to investigate the effect of strength training on mitochondrial proteins and indicators of muscle cellular stress in PCa patients on ADT.

          Methods

          Men diagnosed with locally advanced PCa receiving ADT were randomised to a strength training group (STG) ( n=16) or a control group (CG) ( n=15) for 16 weeks. Muscle biopsies were collected pre- and post-intervention from the vastus lateralis muscle, and analysed for mitochondrial proteins (citrate synthase, cytochrome c oxidase subunit IV (COXIV), HSP60) and indicators of muscle cellular stress (heat shock protein (HSP) 70, alpha B-crystallin, HSP27, free ubiquitin, and total ubiquitinated proteins) using Western blot and ELISA.

          Results

          No significant intervention effects were observed in any of the mitochondrial proteins or indicators of muscle cellular stress. However, within-group analysis revealed that the level of HSP70 was reduced in the STG and a tendency towards a reduction in citrate synthase levels was observed in the CG. Levels of total ubiquitinated proteins were unchanged in both groups.

          Conclusion

          Although reduced HSP70 levels indicated reduced muscle cellular stress in the STG, the lack of an intervention effect precluded any clear conclusions.

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          Most cited references23

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          Molecular chaperones in cellular protein folding.

          F U Hartl (1996)
          The folding of many newly synthesized proteins in the cell depends on a set of conserved proteins known as molecular chaperones. These prevent the formation of misfolded protein structures, both under normal conditions and when cells are exposed to stresses such as high temperature. Significant progress has been made in the understanding of the ATP-dependent mechanisms used by the Hsp70 and chaperonin families of molecular chaperones, which can cooperate to assist in folding new polypeptide chains.
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            • Abstract: found
            • Article: not found

            The concept of symmorphosis: a testable hypothesis of structure-function relationship.

            The hypothesis that, in biological organisms, structural design is matched to functional demand is difficult to test because it is largely based on anecdotal evidence suggesting economic design. The hypothesis of symmorphosis postulates a quantitative match of design and function parameters within a defined functional system; because of its stringency it is refutable and can, therefore, be subjected to empirical test, for example, by assessing whether the structures that support the pathway for oxygen from the lung to the consumer in muscle cells are quantitatively adjusted to the limit of functional performance of the respiratory system. The study of allometric and adaptive variation leads to the conclusion that the hypothesis of symmorphosis is acceptable for all internal compartments of the respiratory system (blood, heart, muscle capillaries, and mitochondria), whereas it must be refuted for the lung that forms the interface to the environment.
              • Record: found
              • Abstract: not found
              • Article: not found

              Heat shock, stress proteins, chaperones, and proteotoxicity.

                Author and article information

                Journal
                Endocr Connect
                Endocr Connect
                EC
                Endocrine Connections
                Bioscientifica Ltd (Bristol )
                2049-3614
                March 2016
                01 March 2016
                : 5
                : 2
                : 74-82
                Affiliations
                [1 ]Department of Physical Performance Norwegian School of Sports Sciences, Oslo, Norway
                [2 ]Department of Oncology Oslo University Hospital, Oslo, Norway
                Author notes
                Correspondence should be addressed to T S Nilsen; Email: t.s.nilsen@ 123456nih.no
                Article
                EC150120
                10.1530/EC-15-0120
                5002963
                27169606
                72395169-e9cc-4463-a22c-d2179d3573ac
                © 2016 The authors

                This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

                History
                : 23 February 2016
                : 29 February 2016
                Categories
                Research

                androgen deprivation therapy,exercise,cellular stress,heat shock proteins,mitochondria,citrate synthase,coxiv,ubiquitin

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