Consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes

Introduction: Loss of muscle is common in patients with advanced non-small cell lung cancer (NSCLC), and contributes to the high morbidity and mortality of this group. The exact mechanisms behind the loss of muscle are unclear. Patients and methods: To investigate this, 4 patients with stage IV NS...

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Main Authors: Murton, Andrew J., Maddocks, Matthew, Stephens, Francis B., Marimuthu, Kanagaraj, England, Ruth, Wilcock, Andrew
Format: Article
Published: Elsevier 2016
Subjects:
Online Access:https://eprints.nottingham.ac.uk/35817/
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author Murton, Andrew J.
Maddocks, Matthew
Stephens, Francis B.
Marimuthu, Kanagaraj
England, Ruth
Wilcock, Andrew
author_facet Murton, Andrew J.
Maddocks, Matthew
Stephens, Francis B.
Marimuthu, Kanagaraj
England, Ruth
Wilcock, Andrew
author_sort Murton, Andrew J.
building Nottingham Research Data Repository
collection Online Access
description Introduction: Loss of muscle is common in patients with advanced non-small cell lung cancer (NSCLC), and contributes to the high morbidity and mortality of this group. The exact mechanisms behind the loss of muscle are unclear. Patients and methods: To investigate this, 4 patients with stage IV NSCLC meeting the clinical definitions for sarcopenia and cachexia were recruited, along with 4 age-matched healthy volunteers. Following an overnight fast, biopsies were obtained from the vastus lateralis and key components associated with inflammation and the control of muscle protein, carbohydrate and fat metabolism assessed. Results: Compared to healthy volunteers, significant increases in mRNA levels for interleukin-6 and NFκB signalling were observed in NSCLC patients along with lower intramyocellular lipid content in slow-twitch fibres. While a significant decrease in phosphorylation of mTOR signalling protein 4E-BP1 (Ser65) was observed along with a trend towards reduced p70 S6K (Thr389) phosphorylation (P=0.06), there was no difference between groups for mRNA levels of MAFbx and MuRF1, chymotrypsin-like activity of the proteasome, or protein levels of multiple proteasome subunits. Moreover, despite decreases in intramyocellular lipid content, no robust changes in mRNA levels for key proteins involved in insulin signalling, glycolysis, oxidative metabolism or fat metabolism were observed. Conclusions: These findings suggest that an examination of the contribution of suppressed mTOR signalling in the loss of muscle mass in late-stage NSCLC patients is warranted and reinforces our need to understand the potential contribution of impaired fat metabolism and muscle protein synthesis in the aetiology of cancer cachexia.
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spelling nottingham-358172020-05-04T17:55:16Z https://eprints.nottingham.ac.uk/35817/ Consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes Murton, Andrew J. Maddocks, Matthew Stephens, Francis B. Marimuthu, Kanagaraj England, Ruth Wilcock, Andrew Introduction: Loss of muscle is common in patients with advanced non-small cell lung cancer (NSCLC), and contributes to the high morbidity and mortality of this group. The exact mechanisms behind the loss of muscle are unclear. Patients and methods: To investigate this, 4 patients with stage IV NSCLC meeting the clinical definitions for sarcopenia and cachexia were recruited, along with 4 age-matched healthy volunteers. Following an overnight fast, biopsies were obtained from the vastus lateralis and key components associated with inflammation and the control of muscle protein, carbohydrate and fat metabolism assessed. Results: Compared to healthy volunteers, significant increases in mRNA levels for interleukin-6 and NFκB signalling were observed in NSCLC patients along with lower intramyocellular lipid content in slow-twitch fibres. While a significant decrease in phosphorylation of mTOR signalling protein 4E-BP1 (Ser65) was observed along with a trend towards reduced p70 S6K (Thr389) phosphorylation (P=0.06), there was no difference between groups for mRNA levels of MAFbx and MuRF1, chymotrypsin-like activity of the proteasome, or protein levels of multiple proteasome subunits. Moreover, despite decreases in intramyocellular lipid content, no robust changes in mRNA levels for key proteins involved in insulin signalling, glycolysis, oxidative metabolism or fat metabolism were observed. Conclusions: These findings suggest that an examination of the contribution of suppressed mTOR signalling in the loss of muscle mass in late-stage NSCLC patients is warranted and reinforces our need to understand the potential contribution of impaired fat metabolism and muscle protein synthesis in the aetiology of cancer cachexia. Elsevier 2016-06-25 Article PeerReviewed Murton, Andrew J., Maddocks, Matthew, Stephens, Francis B., Marimuthu, Kanagaraj, England, Ruth and Wilcock, Andrew (2016) Consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes. Clinical Lung Cancer . ISSN 1525-7304 Muscle protein synthesis; proteolysis; cachexia; mTOR signalling; ubiquitin proteasome system http://www.sciencedirect.com/science/article/pii/S1525730416301437 doi:10.1016/j.cllc.2016.06.003 doi:10.1016/j.cllc.2016.06.003
spellingShingle Muscle protein synthesis; proteolysis; cachexia; mTOR signalling; ubiquitin proteasome system
Murton, Andrew J.
Maddocks, Matthew
Stephens, Francis B.
Marimuthu, Kanagaraj
England, Ruth
Wilcock, Andrew
Consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes
title Consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes
title_full Consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes
title_fullStr Consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes
title_full_unstemmed Consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes
title_short Consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes
title_sort consequences of late-stage non-small cell lung cancer cachexia on muscle metabolic processes
topic Muscle protein synthesis; proteolysis; cachexia; mTOR signalling; ubiquitin proteasome system
url https://eprints.nottingham.ac.uk/35817/
https://eprints.nottingham.ac.uk/35817/
https://eprints.nottingham.ac.uk/35817/