Evidence map›Paper›PMID 35199910›Full record

ArticleEMBO reports2022

Iron supplementation is sufficient to rescue skeletal muscle mass and function in cancer cachexia.

Elisabeth Wyart, Myriam Y Hsu, Roberta Sartori, Erica Mina, Valentina Rausch, Elisa S Pierobon, Mariarosa Mezzanotte, Camilla Pezzini, Laure B Bindels, Andrea Lauria and 10 more

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.9field-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

41 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Observational
  7. HUWE1 in Skeletal Muscle Prevents Muscle Fatigue via Maintaining Iron and Calcium Homeostasis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

20 authors at 5 institutions in 2 countries.

Elisabeth Wyart *Department of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.ORCID 0000-0002-2468-5396
Myriam Y Hsu *Department of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.ORCID 0000-0001-5198-7368
Roberta SartoriDepartment of Biomedical Sciences, University of Padova, Padova, Italy.ORCID 0000-0002-2763-9838
Erica MinaDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.
Valentina RauschDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.
Elisa S PierobonDepartment of Surgical, Oncological and Gastroenterological Sciences, Padova University Hospital, Padova, Italy.ORCID 0000-0002-5836-1197
Mariarosa MezzanotteDepartment of Clinical and Biological Sciences, University of Torino, Turin, Italy.
Camilla PezziniDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Laure B BindelsMetabolism and Nutrition Research Group, Louvain Drug Research Institute, Université catholique de Louvain (UCLouvain), Brussels, Belgium.ORCID 0000-0003-3747-3234
Andrea LauriaDepartment of Life Sciences and System Biology, University of Torino, Turin, Italy.
Fabio PennaDepartment of Clinical and Biological Sciences, University of Torino, Turin, Italy.
Emilio HirschDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.
Miriam MartiniDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.
Massimiliano MazzoneDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.ORCID 0000-0001-8824-4015
Antonella RoettoDepartment of Clinical and Biological Sciences, University of Torino, Turin, Italy.
Simonetta Geninatti CrichDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.
Hans PrenenDepartment of Medical Oncology, University Hospital Antwerp, Edegem, Belgium.ORCID 0000-0001-8802-7352
Marco SandriDepartment of Biomedical Sciences, University of Padova, Padova, Italy.
Alessio Menga *Department of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.
Paolo E Porporato *Department of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.ORCID 0000-0001-8519-1552
University of Turin · ITUniversity of Padua · ITUCLouvain · BEUniversity of Antwerp · BEVlaams Instituut voor Biotechnologie · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cachexia is a wasting syndrome characterized by devastating skeletal muscle atrophy that dramatically increases mortality in various diseases, most notably in cancer patients with a penetrance of up to 80%. Knowledge regarding the mechanism of cancer-induced cachexia remains very scarce, making cachexia an unmet medical need. In this study, we discovered strong alterations of iron metabolism in the skeletal muscle of both cancer patients and tumor-bearing mice, characterized by decreased iron availability in mitochondria. We found that modulation of iron levels directly influences myotube size in vitro and muscle mass in otherwise healthy mice. Furthermore, iron supplementation was sufficient to preserve both muscle function and mass, prolong survival in tumor-bearing mice, and even rescues strength in human subjects within an unexpectedly short time frame. Importantly, iron supplementation refuels mitochondrial oxidative metabolism and energy production. Overall, our findings provide new mechanistic insights in cancer-induced skeletal muscle wasting, and support targeting iron metabolism as a potential therapeutic option for muscle wasting diseases.

Indexed as

CachexiaNeoplasmsAnimalsDietary SupplementsHumansIronMiceMuscle, SkeletalIroncachexiaironmetabolismmitochondriamuscle

Identifiers

PMID35199910
PMCPMC8982578
OpenAlexW4213426762

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.