Evidence map›Paper›PMID 35008253›Full record

ArticleCancers2021

Aging Aggravates Cachexia in Tumor-Bearing Mice.

Julia Geppert, Alina A Walth, Raúl Terrón Expósito, Doris Kaltenecker, Pauline Morigny, Juliano Machado, Maike Becker, Estefania Simoes, Joanna D C C Lima, Carolin Daniel and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
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  6. Review
  7. Hallmarks of Cancer Cachexia: Sexual Dimorphism in Related Pathways.International journal of molecular sciences · 2025
    Review
  8. Article
  9. Diversity in chemotherapy-induced cachexia.American journal of physiology. Cell physiology · 2025
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Cancer cachexia as a multiorgan failure: Reconstruction of the crime scene.Frontiers in cell and developmental biology · 2022
    Review
  19. Article
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

14 authors at 3 institutions in 2 countries.

Julia GeppertInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.
Alina A WalthInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.
Raúl Terrón ExpósitoInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.
Doris KalteneckerInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.
Pauline MorignyInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.
Juliano MachadoInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.
Maike BeckerGerman Center for Diabetes Research (DZD), 85764 Neuherberg, Germany.ORCID 0000-0001-6416-4213
Estefania SimoesInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.ORCID 0000-0002-2842-5030
Joanna D C C LimaDepartment of Surgery and LIM 26, Faculdade de Medicina, University of Sao Paulo, Sao Paulo 01246-903, Brazil.ORCID 0000-0001-6804-8666
Carolin DanielGerman Center for Diabetes Research (DZD), 85764 Neuherberg, Germany.
Mauricio Berriel DiazInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.ORCID 0000-0003-4670-919X
Stephan HerzigInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.
Marilia SeelaenderDepartment of Surgery and LIM 26, Faculdade de Medicina, University of Sao Paulo, Sao Paulo 01246-903, Brazil.
Maria RohmInstitute for Diabetes and Cancer, Helmholtz Center Munich, 85764 Neuherberg, Germany.ORCID 0000-0003-3926-1534
Heidelberg University · DEUniversidade de São Paulo · BRDeutsches Diabetes-Zentrum e.V. · DE

Funding

Austrian Science Fund FWF J 4224
6 · The paper itself

Abstract

backgroundCancer is primarily a disease of high age in humans, yet most mouse studies on cancer cachexia are conducted using young adolescent mice. Given that metabolism and muscle function change with age, we hypothesized that aging may affect cachexia progression in mouse models.

methodsWe compare tumor and cachexia development in young and old mice of three different strains (C57BL/6J, C57BL/6N, BALB/c) and with two different tumor cell lines (Lewis Lung Cancer, Colon26). Tumor size, body and organ weights, fiber cross-sectional area, circulating cachexia biomarkers, and molecular markers of muscle atrophy and adipose tissue wasting are shown. We correlate inflammatory markers and body weight dependent on age in patients with cancer.

resultsWe note fundamental differences between mouse strains. Aging aggravates weight loss in LLC-injected C57BL/6J mice, drives it in C57BL/6N mice, and does not influence weight loss in C26-injected BALB/c mice. Glucose tolerance is unchanged in cachectic young and old mice. The stress marker GDF15 is elevated in cachectic BALB/c mice independent of age and increased in old C57BL/6N and J mice. Inflammatory markers correlate significantly with weight loss only in young mice and patients.

conclusionsAging affects cachexia development and progression in mice in a strain-dependent manner and influences the inflammatory profile in both mice and patients. Age is an important factor to consider for future cachexia studies.

Indexed as

agingcachexiacancermouse models

Identifiers

PMID35008253
PMCPMC8750471
OpenAlexW4200576689

What OpenQuestion holds

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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.