Interleukin-6 initiates muscle- and adipose tissue wasting in a novel C57BL/6 model of cancer-associated cachexia.


Journal

Journal of cachexia, sarcopenia and muscle
ISSN: 2190-6009
Titre abrégé: J Cachexia Sarcopenia Muscle
Pays: Germany
ID NLM: 101552883

Informations de publication

Date de publication:
02 2023
Historique:
revised: 23 08 2022
received: 20 01 2022
accepted: 26 09 2022
pubmed: 10 11 2022
medline: 4 2 2023
entrez: 9 11 2022
Statut: ppublish

Résumé

Cancer-associated cachexia (CAC) is a wasting syndrome drastically reducing efficacy of chemotherapy and life expectancy of patients. CAC affects up to 80% of cancer patients, yet the mechanisms underlying the disease are not well understood and no approved disease-specific medication exists. As a multiorgan disorder, CAC can only be studied on an organismal level. To cover the diverse aetiologies of CAC, researchers rely on the availability of a multifaceted pool of cancer models with varying degrees of cachexia symptoms. So far, no tumour model syngeneic to C57BL/6 mice exists that allows direct comparison between cachexigenic- and non-cachexigenic tumours. MCA207 and CHX207 fibrosarcoma cells were intramuscularly implanted into male or female, 10-11-week-old C57BL/6J mice. Tumour tissues were subjected to magnetic resonance imaging, immunohistochemical-, and transcriptomic analysis. Mice were analysed for tumour growth, body weight and -composition, food- and water intake, locomotor activity, O CHX207, but not MCA207-tumour-bearing mice exhibited major clinical features of CAC, including systemic inflammation, increased plasma IL-6 concentrations (190 pg/mL, P ≤ 0.0001), increased energy expenditure (+28%, P ≤ 0.01), adipose tissue loss (-47%, P ≤ 0.0001), skeletal muscle wasting (-18%, P ≤ 0.001), and body weight reduction (-13%, P ≤ 0.01) 13 days after cancer cell inoculation. Adipose tissue loss resulted from reduced lipid uptake and -synthesis combined with increased lipolysis but was not associated with elevated beta-adrenergic signalling or adipose tissue browning. Muscle atrophy was evident by reduced myofibre cross sectional area (-21.8%, P ≤ 0.001), increased catabolic- and reduced anabolic signalling. Deletion of IL-6 from CHX207 cancer cells completely protected CHX207 In this study, we present CHX207 fibrosarcoma cells as a novel tool to investigate the mediators and metabolic consequences of CAC in C57BL/6 mice in comparison to non-cachectic MCA207-tumour-bearing mice. IL-6 represents an essential trigger for CAC development in CHX207-tumour-bearing mice.

Sections du résumé

BACKGROUND
Cancer-associated cachexia (CAC) is a wasting syndrome drastically reducing efficacy of chemotherapy and life expectancy of patients. CAC affects up to 80% of cancer patients, yet the mechanisms underlying the disease are not well understood and no approved disease-specific medication exists. As a multiorgan disorder, CAC can only be studied on an organismal level. To cover the diverse aetiologies of CAC, researchers rely on the availability of a multifaceted pool of cancer models with varying degrees of cachexia symptoms. So far, no tumour model syngeneic to C57BL/6 mice exists that allows direct comparison between cachexigenic- and non-cachexigenic tumours.
METHODS
MCA207 and CHX207 fibrosarcoma cells were intramuscularly implanted into male or female, 10-11-week-old C57BL/6J mice. Tumour tissues were subjected to magnetic resonance imaging, immunohistochemical-, and transcriptomic analysis. Mice were analysed for tumour growth, body weight and -composition, food- and water intake, locomotor activity, O
RESULTS
CHX207, but not MCA207-tumour-bearing mice exhibited major clinical features of CAC, including systemic inflammation, increased plasma IL-6 concentrations (190 pg/mL, P ≤ 0.0001), increased energy expenditure (+28%, P ≤ 0.01), adipose tissue loss (-47%, P ≤ 0.0001), skeletal muscle wasting (-18%, P ≤ 0.001), and body weight reduction (-13%, P ≤ 0.01) 13 days after cancer cell inoculation. Adipose tissue loss resulted from reduced lipid uptake and -synthesis combined with increased lipolysis but was not associated with elevated beta-adrenergic signalling or adipose tissue browning. Muscle atrophy was evident by reduced myofibre cross sectional area (-21.8%, P ≤ 0.001), increased catabolic- and reduced anabolic signalling. Deletion of IL-6 from CHX207 cancer cells completely protected CHX207
CONCLUSIONS
In this study, we present CHX207 fibrosarcoma cells as a novel tool to investigate the mediators and metabolic consequences of CAC in C57BL/6 mice in comparison to non-cachectic MCA207-tumour-bearing mice. IL-6 represents an essential trigger for CAC development in CHX207-tumour-bearing mice.

Identifiants

pubmed: 36351437
doi: 10.1002/jcsm.13109
pmc: PMC9891934
doi:

Substances chimiques

Interleukin-6 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

93-107

Subventions

Organisme : Leducq Foundation
Organisme : Louis Jeantet Foundation
Organisme : DK Molecular Enzymology
ID : W901
Organisme : Austrian Science Fund
ID : F83
Organisme : Austrian Science Fund
ID : F7302
Organisme : Austrian Science Fund
ID : P30968
Organisme : Austrian Science Fund
ID : I5618
Organisme : DOC fellowship
ID : 25049
Organisme : aH2020-MSCA-ITN
ID : 859860
Organisme : BioTechMed-Flagship Project 'Midas'
Organisme : University of Graz
Organisme : Medical University of Vienna
Organisme : European Research Council
ID : 340896
Pays : International

Informations de copyright

© 2022 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders.

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Auteurs

Isabella Pototschnig (I)

Institute of Molecular Biosciences, University of Graz, Graz, Austria.

Ursula Feiler (U)

Institute of Molecular Biosciences, University of Graz, Graz, Austria.

Clemens Diwoky (C)

Institute of Molecular Biosciences, University of Graz, Graz, Austria.

Paul W Vesely (PW)

Diagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.

Thomas Rauchenwald (T)

Institute of Molecular Biosciences, University of Graz, Graz, Austria.

Margret Paar (M)

Division of Physiological Chemistry, Otto-Loewi Research Center, Medical University of Graz, Graz, Austria.

Latifa Bakiri (L)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Laura Pajed (L)

Institute of Molecular Biosciences, University of Graz, Graz, Austria.

Peter Hofer (P)

Institute of Molecular Biosciences, University of Graz, Graz, Austria.

Karl Kashofer (K)

Diagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.

Nyamdelger Sukhbaatar (N)

Institute of Medical Genetics, Medical University of Vienna, Vienna, Austria.

Gabriele Schoiswohl (G)

Department of Pharmacology and Toxicology, University of Graz, Graz, Austria.

Thomas Weichhart (T)

Institute of Medical Genetics, Medical University of Vienna, Vienna, Austria.

Gerald Hoefler (G)

Diagnostic and Research Institute of Pathology, Medical University of Graz, Graz, Austria.
BioTechMed-Graz, Graz, Austria.

Christoph Bock (C)

CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Institute of Artificial Intelligence, Center for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna, Vienna, Austria.

Martin Pichler (M)

Division of Oncology, Medical University of Graz, Austria.

Erwin F Wagner (EF)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Department of Dermatology, Medical University of Vienna, Vienna, Austria.

Rudolf Zechner (R)

Institute of Molecular Biosciences, University of Graz, Graz, Austria.
BioTechMed-Graz, Graz, Austria.
Field of Excellence BioHealth - University of Graz, Graz, Austria.

Martina Schweiger (M)

Institute of Molecular Biosciences, University of Graz, Graz, Austria.
BioTechMed-Graz, Graz, Austria.
Field of Excellence BioHealth - University of Graz, Graz, Austria.

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