Evidence map›Paper›PMID 32041358›Full record

ArticleInternational journal of molecular sciences2020

Displaced Myonuclei in Cancer Cachexia Suggest Altered Innervation.

Nissrine Daou, Medhi Hassani, Emidio Matos, Gabriela Salim De Castro, Raquel Galvao Figueredo Costa, Marilia Seelaender, Viviana Moresi, Marco Rocchi, Sergio Adamo, Zhenlin Li and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Myonuclear Dynamics After Skeletal Muscle Surgical Injury.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Physical Activity, Exerkines, and Their Role in Cancer Cachexia.International journal of molecular sciences · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

Nissrine DaouSorbonne Université, Institut de Biologie Paris-Seine (IBPS), CNRS UMR 8256, Inserm ERL U1164, Biological Adaptation and Ageing, F-75005 Paris, France.
Medhi HassaniSorbonne Université, Institut de Biologie Paris-Seine (IBPS), CNRS UMR 8256, Inserm ERL U1164, Biological Adaptation and Ageing, F-75005 Paris, France.
Emidio MatosDepartment of Physical Education, Federal University of Piauí, Piauí 64000-805 PI, Brazil.
Gabriela Salim De CastroInstitute of Biomedical Sciences, University of Sao Paulo, Sao Paulo 05508-000 SP, Brazil.
Raquel Galvao Figueredo CostaInstitute of Biomedical Sciences, University of Sao Paulo, Sao Paulo 05508-000 SP, Brazil.
Marilia SeelaenderInstitute of Biomedical Sciences, University of Sao Paulo, Sao Paulo 05508-000 SP, Brazil.
Viviana MoresiDAHFMO Unit of Histology and Medical Embryology, Sapienza University of Rome, 00161 Rome, Italy.
Marco RocchiDepartment of Biomolecular Sciences, University of Urbino Carlo Bo, 61029 Urbino, Italy.
Sergio AdamoDAHFMO Unit of Histology and Medical Embryology, Sapienza University of Rome, 00161 Rome, Italy.
Zhenlin LiSorbonne Université, Institut de Biologie Paris-Seine (IBPS), CNRS UMR 8256, Inserm ERL U1164, Biological Adaptation and Ageing, F-75005 Paris, France.
Onnik AgbulutSorbonne Université, Institut de Biologie Paris-Seine (IBPS), CNRS UMR 8256, Inserm ERL U1164, Biological Adaptation and Ageing, F-75005 Paris, France.
Dario ColettiSorbonne Université, Institut de Biologie Paris-Seine (IBPS), CNRS UMR 8256, Inserm ERL U1164, Biological Adaptation and Ageing, F-75005 Paris, France.
Centre National de la Recherche Scientifique · FRUniversidade de São Paulo · BRSapienza University of Rome · ITUniversidade Federal do Piauí · BRUniversity of Urbino · IT

Funding

Agence Nationale de la Recherche 13-BSV1-0005Agence Nationale de la Recherche 17-CE17-0015-01Association Française contre les Myopathies 16282Association Française contre les Myopathies 20603-2017IBPS Sorbonne Université 2015 ColettiMinistero dell'Istruzione, dell'Università e della Ricerca PRIN 2009WBFZYM 001Ministero dell'Istruzione, dell'Università e della Ricerca PRIN 2012N8YJC3NIH HHS 5R01CA180057-02Sapienza Università di Roma Avvio alla Ricerca 2019 to MHUIF - Università Italo-Francese VINCI 2018 to MH
6 · The paper itself

Abstract

An idiopathic myopathy characterized by central nuclei in muscle fibers, a hallmark of muscle regeneration, has been observed in cancer patients. In cancer cachexia skeletal muscle is incapable of regeneration, consequently, this observation remains unaccounted for. In C26-tumor bearing, cachectic mice, we observed muscle fibers with central nuclei in the absence of molecular markers of bona fide regeneration. These clustered, non-peripheral nuclei were present in NCAM-expressing muscle fibers. Since NCAM expression is upregulated in denervated myofibers, we searched for additional makers of denervation, including AchRs, MUSK, and HDAC. This last one being also consistently upregulated in cachectic muscles, correlated with an increase of central myonuclei. This held true in the musculature of patients suffering from gastrointestinal cancer, where a progressive increase in the number of central myonuclei was observed in weight stable and in cachectic patients, compared to healthy subjects. Based on all of the above, the presence of central myonuclei in cancer patients and animal models of cachexia is consistent with motor neuron loss or NMJ perturbation and could underlie a previously neglected phenomenon of denervation, rather than representing myofiber damage and regeneration in cachexia. Similarly to aging, denervation-dependent myofiber atrophy could contribute to muscle wasting in cancer cachexia.

Indexed as

AnimalsBiomarkersCachexiaCell Line, TumorColonic NeoplasmsDisease Models, AnimalFemaleHistone DeacetylasesMiceMuscle Fibers, SkeletalMuscle, SkeletalNeoplasm TransplantationBiomarkersHistone Deacetylasesaltered innervationc26-colon carcinomacancer cachexiaCentral nucleimuscle regenerationstriated muscles

Identifiers

PMID32041358
PMCPMC7038037
OpenAlexW3005465464

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.