Evidence map›Paper›PMID 38183352›Full record

ArticleJournal of cachexia, sarcopenia and muscle2024

A single chemotherapy administration induces muscle atrophy, mitochondrial alterations and apoptosis in breast cancer patients.

Joris Mallard, Elyse Hucteau, Laura Bender, Fabien Moinard-Butot, Emma Rochelle, Lauréline Boutonnet, Antoine Grandperrin, Roland Schott, Carole Pflumio, Philippe Trensz and 7 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 18 citations in OpenAlex.

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  9. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
    Article
  10. Cancer cachexia: molecular basis and therapeutic advances.Signal transduction and targeted therapy · 2026
    Review
  11. Review
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  14. Factors responsible for the decline in physical fitness during neoadjuvant chemotherapy in older patients with esophageal cancer: an exploratory prospective cohort study.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Article
  15. Clinical mechanism of muscle mass loss during neoadjuvant chemotherapy in older patients with esophageal cancer: a prospective cohort study.Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus · 2025
    Article
  16. 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

17 authors at 2 institutions in 1 country.

Joris MallardBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.ORCID 0009-0009-0890-3136
Elyse HucteauBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.
Laura BenderInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Fabien Moinard-ButotInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Emma RochelleBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.
Lauréline BoutonnetBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.
Antoine GrandperrinBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.
Roland SchottInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Carole PflumioInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Philippe TrenszInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Michal Kalish-WeindlingInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Anne-Laure CharlesBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.
Bernard GényBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.
Fabrice FavretBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.
Xavier PivotInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Thomas J HureauBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.
Allan F PaganoBiomedicine Research Center of Strasbourg (CRBS), UR 3072, "Mitochondrie, Stress oxydant et Plasticité musculaire", University of Strasbourg, Strasbourg, France.
Institut de Cancérologie Strasbourg · FRMitochondrie, stress oxydant et protection musculaire · FR

Funding

Institut de Cancérologie Strasbourg Europe (ICANS)Investments in the Future programme of the French government (IdEx Unistra)OCOVAS
6 · The paper itself

Abstract

backgroundBreast cancer patients are commonly treated with sequential administrations of epirubicin-cyclophosphamide (EC) and paclitaxel (TAX). The chronic effect of this treatment induces skeletal muscle alterations, but the specific effect of each chemotherapy agent is unknown. This study aimed to investigate the effect of EC or TAX administration on skeletal muscle homeostasis in breast cancer patients.

methodsTwenty early breast cancer patients undergoing EC followed by TAX chemotherapies were included. Two groups of 10 women were established and performed vastus lateralis skeletal muscle biopsies either before the first administration (pre) of EC (50 ± 14 years) or TAX (50 ± 16 years) and 4 days later (post). Mitochondrial respiratory capacity recording, reactive oxygen species production, western blotting and histological analyses were performed.

resultsDecrease in muscle fibres cross-sectional area was only observed post-EC (-25%; P < 0.001), associated with a reduction in mitochondrial respiratory capacity for the complex I (CI)-linked substrate state (-32%; P = 0.001), oxidative phosphorylation (OXPHOS) by CI (-35%; P = 0.002), CI&CII (-26%; P = 0.022) and CII (-24%; P = 0.027). If H

conclusionsWe demonstrated that a single administration of EC induced, in only 4 days, skeletal muscle atrophy and mitochondrial alterations in breast cancer patients. These alterations were characterized by reductions in mitochondrial function and content as well as impairment of mitochondrial dynamics and an increase in apoptosis. TAX administration did not worsen these alterations as this group had already received EC during the preceding weeks. However, it resulted in an increased apoptosis, likely in response to the increased H

Indexed as

Breast NeoplasmsApoptosisElectron Transport Complex IFemaleHumansMitochondriaMuscle, SkeletalMuscular AtrophyElectron Transport Complex IAnthracycline-cyclophosphamideMitochondriaMitochondrial respirationMuscle biopsiesSkeletal muscle deconditioningTaxanes

Identifiers

PMID38183352
PMCPMC10834353
OpenAlexW4390639578

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.