Evidence map›Paper›PMID 35373507›Full record

ArticleJournal of cachexia, sarcopenia and muscle2022

Chemotherapy impairs skeletal muscle mitochondrial homeostasis in early breast cancer patients.

Joris Mallard, Elyse Hucteau, Anne-Laure Charles, Laura Bender, Claire Baeza, Mathilde Pélissie, Philippe Trensz, Carole Pflumio, Michal Kalish-Weindling, Bernard Gény and 5 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 7% 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.

NCT04638712 nacompletednot on this map

Impact of (Neo)Adjuvant Therapy Associating Anthracyclines and Taxanes With or Without Trastuzumab on Skeletal Muscle in Breast Cancer Patients

TypeinterventionalSponsorInstitut de cancérologie Strasbourg EuropeRan2020 to 2021Enrolled13ConditionsBreast CancerArmsMicrobiopsy sample, Muscle echography, Maximal strength, Body composition, Quality of life and Physical activity level
NCT07484776 naactive not recruitingnot on this mapstarted 2026, after this paper: background citation

Metabolic Flexibility in Patients With Early Triple-negative Breast Cancer and the Possible Effect of a Physical Exercise Intervention

TypeinterventionalSponsorUniversidad Europea de MadridRan2026 to 2028Enrolled40ConditionsTriple-Negative Breast Cancer (TNBC)ArmsCardiovascular training at maximal fat oxidation (FATmax), Cardiovascular training at maximal aerobic power (MAP), Resistance training
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 40 citations in OpenAlex.

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  7. An exploratory analysis of 24-h movement behaviors in individuals with cancer completing a 12-week resistance exercise intervention.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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  10. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
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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

15 authors at 2 institutions in 1 country.

Joris MallardFaculté de médecine, maïeutique et sciences de la santé, "Mitochondrie, Stress oxydant, Protection musculaire", Université de Strasbourg, Strasbourg, France.
Elyse HucteauFaculté de médecine, maïeutique et sciences de la santé, "Mitochondrie, Stress oxydant, Protection musculaire", Université de Strasbourg, Strasbourg, France.
Anne-Laure CharlesFaculté de médecine, maïeutique et sciences de la santé, "Mitochondrie, Stress oxydant, Protection musculaire", Université de Strasbourg, Strasbourg, France.
Laura BenderInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Claire BaezaInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Mathilde PélissieInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Philippe TrenszInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Carole PflumioInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Michal Kalish-WeindlingInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Bernard GényFaculté de médecine, maïeutique et sciences de la santé, "Mitochondrie, Stress oxydant, Protection musculaire", Université de Strasbourg, Strasbourg, France.
Roland SchottInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Fabrice FavretFaculté de médecine, maïeutique et sciences de la santé, "Mitochondrie, Stress oxydant, Protection musculaire", Université de Strasbourg, Strasbourg, France.
Xavier PivotInstitut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.
Thomas J HureauFaculté de médecine, maïeutique et sciences de la santé, "Mitochondrie, Stress oxydant, Protection musculaire", Université de Strasbourg, Strasbourg, France.
Allan F PaganoFaculté de médecine, maïeutique et sciences de la santé, "Mitochondrie, Stress oxydant, Protection musculaire", Université de Strasbourg, Strasbourg, France.ORCID 0000-0003-0717-2377
Institut de Cancérologie Strasbourg · FRMitochondrie, stress oxydant et protection musculaire · FR

Funding

Institut de Cancérologie Strasbourg Europe (ICANS) and University of Strasbourg
6 · The paper itself

Abstract

backgroundChemotherapy is extensively used to treat breast cancer and is associated with skeletal muscle deconditioning, which is known to reduce patients' quality of life, treatment efficiency, and overall survival. To date, skeletal muscle mitochondrial alterations represent a major aspect explored in breast cancer patients; nevertheless, the cellular mechanisms remain relatively unknown. This study was dedicated to investigating overall skeletal muscle mitochondrial homeostasis in early breast cancer patients undergoing chemotherapy, including mitochondrial quantity, function, and dynamics.

methodsWomen undergoing (neo)adjuvant anthracycline-cyclophosphamide and taxane-based chemotherapy participated in this study (56 ± 12 years). Two muscle biopsies were collected from the vastus lateralis muscle before the first and after the last chemotherapy administration. Mitochondrial respiratory capacity, reactive oxygen species production, and western blotting analyses were performed.

resultsAmong the 11 patients, we found a decrease in key markers of mitochondrial quantity, reaching -52.0% for citrate synthase protein levels (P = 0.02) and -38.2% for VDAC protein levels (P = 0.04). This mitochondrial content loss is likely explained by reduced mitochondrial biogenesis, as evidenced by a decrease in PGC-1α1 protein levels (-29.5%; P = 0.04). Mitochondrial dynamics were altered, as documented by a decrease in MFN2 protein expression (-33.4%; P = 0.01), a key marker of mitochondrial outer membrane fusion. Mitochondrial fission is a prerequisite for mitophagy activation, and no variation was found in either key markers of mitochondrial fission (Fis1 and DRP1) or mitophagy (Parkin, PINK1, and Mul1). Two contradictory hypotheses arise from these results: defective mitophagy, which probably increases the number of damaged and fragmented mitochondria, or a relative increase in mitophagy through elevated mitophagic potential (Parkin/VDAC ratio; +176.4%; P < 0.02). Despite no change in mitochondrial respiratory capacity and COX IV protein levels, we found an elevation in H

conclusionsThis study demonstrated major mitochondrial alterations subsequent to chemotherapy in early breast cancer patients: (i) a striking reduction in mitochondrial biogenesis, (ii) altered mitochondrial dynamics and potential mitophagy defects, (iii) exacerbated H

Indexed as

Breast NeoplasmsFemaleHomeostasisHumansMitochondriaMuscle, SkeletalQuality of LifeUbiquitin-Protein LigasesUbiquitin-Protein LigasesApoptosisH2O2Mitochondrial biogenesisMitochondrial dynamicsMitophagySkeletal muscle deconditioning

Identifiers

PMID35373507
PMCPMC9178151
OpenAlexW4226038872

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.