Muscle NAD+ depletion and Serpina3n as molecular determinants of murine cancer cachexia – the effects of blocking myostatin and activins

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http://hdl.handle.net/10138/318918

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Hulmi , J J , Penna , F , Pöllänen , N , Nissinen , T A , Hentila , J , Euro , L , Lautaoja , J H , Ballarò , R , Soliymani , R , Baumann , M , Ritvos , O , Pirinen , E & Lalowski , M 2020 , ' Muscle NAD+ depletion and Serpina3n as molecular determinants of murine cancer cachexia – the effects of blocking myostatin and activins ' , Molecular metabolism , vol. 41 , 101046 . https://doi.org/10.1016/j.molmet.2020.101046

Titel: Muscle NAD+ depletion and Serpina3n as molecular determinants of murine cancer cachexia – the effects of blocking myostatin and activins
Författare: Hulmi, Juha J.; Penna, Fabio; Pöllänen, Noora; Nissinen, Tuuli A.; Hentila, Jaakko; Euro, Liliya; Lautaoja, Juulia H.; Ballarò, Riccardo; Soliymani, Rabah; Baumann, Marc; Ritvos, Olli; Pirinen, Eija; Lalowski, Maciej
Upphovmannens organisation: CAMM - Research Program for Clinical and Molecular Metabolism
Faculty of Medicine
University of Helsinki
Research Programs Unit
STEMM - Stem Cells and Metabolism Research Program
Department of Biochemistry and Developmental Biology
Helsinki Institute of Life Science HiLIFE
Marc Baumann / Principal Investigator
University Management
Department of Physiology
Growth factor physiology
Eija Pirinen / Principal Investigator
Datum: 2020-11
Språk: eng
Sidantal: 13
Tillhör serie: Molecular metabolism
ISSN: 2212-8778
DOI: https://doi.org/10.1016/j.molmet.2020.101046
Permanenta länken (URI): http://hdl.handle.net/10138/318918
Abstrakt: Objective Cancer cachexia and muscle loss are associated with increased morbidity and mortality. In preclinical animal models, blocking activin receptor (ACVR) ligands has improved survival and prevented muscle wasting in cancer cachexia without an effect on tumour growth. However, the underlying mechanisms are poorly understood. The present study aimed to identify cancer cachexia and soluble ACVR (sACVR) administration-evoked changes in muscle proteome. Methods Healthy and C26 tumour-bearing (TB) mice were treated with recombinant sACVR. The sACVR or PBS control were administered either prior to the tumour formation or by continued administration before and after tumour formation. Muscles were analysed by quantitative proteomics with further examination of mitochondria and nicotinamide adenine dinucleotide (NAD+) metabolism. To complement the first prophylactic experiment, sACVR (or PBS) was injected as a treatment following tumour cell inoculation. Results Muscle proteomics in TB cachectic mice revealed downregulated signatures for mitochondrial oxidative phosphorylation (OXPHOS) and increased acute phase response (APR). These were accompanied by muscle NAD+ deficiency, alterations in NAD+ biosynthesis including downregulation of nicotinamide riboside kinase 2 (Nrk2), and decreased muscle protein synthesis. The disturbances in NAD+ metabolism and protein synthesis were rescued upontreatment with sACVR. Across the whole proteome and APR in particular, Serpina3n represented the most upregulated protein and the strongest predictor of cachexia. However, the increase in Serpina3n expression associated with increased inflammation rather than decreased muscle mass and/or protein synthesis. Conclusions We present here an evidence implicating disturbed muscle mitochondrial OXPHOS proteome and NAD+ homeostasis in experimental cancer cachexia. Treatment of tumour-bearing mice with a blocker of activin receptor ligands restores depleted muscle NAD+ and Nrk2 as well as decreased muscle protein synthesis. These results point out putative new treatment therapies for cachexia. Our results also reveal that although acute phase protein Serpina3n may serve as a predictor of cachexia, it more likely reflects a condition of elevated inflammation.
Subject: 318 Medical biotechnology
C26
OXPHOS
APR
Nrk2
Activin receptor
Cancer cachexia
C26
Cancer cachexia
Activin receptor
Nrk2
APR
OXPHOS
MUSCULAR-DYSTROPHY
EXPRESSION
METABOLISM
SIRTUINS
REVERSAL
MICE
Referentgranskad: Ja
Licens: cc_by
Användningsbegränsning: openAccess
Parallelpublicerad version: acceptedVersion


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