Evidence map›Paper›PMID 26136193›Full record

ArticleJournal of cachexia, sarcopenia and muscle2015

Febuxostat improves outcome in a rat model of cancer cachexia.

Masaaki Konishi, Loes Pelgrim, Anika Tschirner, Anna Baumgarten, Stephan von Haehling, Sandra Palus, Wolfram Doehner, Stefan D Anker, Jochen Springer

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Cancer cachexia: molecular basis and therapeutic advances.Signal transduction and targeted therapy · 2026
    Review
  3. Review
  4. Article
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  6. Article
  7. Article
  8. Review
  9. Increased Adenine Nucleotide Degradation in Skeletal Muscle Atrophy.International journal of molecular sciences · 2019
    Review
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  11. Article
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  13. 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

9 authors at 3 institutions in 2 countries.

Masaaki KonishiDivision of Innovative Clinical Trials, University Medical Centre Göttingen, Göttingen, Germany.
Loes PelgrimApplied Cachexia Research, Center for Cardiovascular Research, Charité Medical School, Berlin, Germany.
Anika TschirnerApplied Cachexia Research, Center for Cardiovascular Research, Charité Medical School, Berlin, Germany.
Anna BaumgartenApplied Cachexia Research, Center for Cardiovascular Research, Charité Medical School, Berlin, Germany.
Stephan von HaehlingDivision of Innovative Clinical Trials, University Medical Centre Göttingen, Göttingen, Germany.
Sandra PalusDivision of Innovative Clinical Trials, University Medical Centre Göttingen, Göttingen, Germany.
Wolfram DoehnerCenter for Stroke Research Berlin, Charité Medical School, Berlin, Germany.
Stefan D AnkerDivision of Innovative Clinical Trials, University Medical Centre Göttingen, Göttingen, Germany.
Jochen SpringerDivision of Innovative Clinical Trials, University Medical Centre Göttingen, Göttingen, Germany.
Charité - Universitätsmedizin Berlin · DEMSB Medical School Berlin · DEUniversitätsmedizin Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundActivity of xanthine oxidase is induced in cancer cachexia, and its inhibition by allopurinol or oxypurinol improves survival and reduces wasting in the Yoshida hepatoma cancer cachexia model. Here, we tested the effects of the second-generation xanthine oxidase inhibitor febuxostat compared with placebo in the same model as used previously by our group.

methodsWistar rats (~200 g) were treated daily with febuxostat at 5 mg/kg/day or placebo via gavage for a maximum of 17 days. Weight change, quality of life, and body composition were analysed. After sacrifice, proteasome activity in the gastrocnemius muscle was measured. Muscle-specific proteins involved in metabolism were analysed by western blotting.

resultsTreatment of the tumour-bearing rats with febuxostat led to a significantly improved survival compared with placebo (hazard ratio: 0.45, 95% confidence interval: 0.22-0.93, P = 0.03). Loss of body weight was reduced (-26.3 ± 12.4 g) compared with placebo (-50.2 ± 2.1 g, P < 0.01). Wasting of lean mass was attenuated (-12.7 ± 10.8 g) vs. placebo (-31.9 ± 2.1 g, P < 0.05). While we did not see an effect of febuxostat on proteasome activity at the end of the study, the pAkt/Akt ratio was improved by febuxostat (0.94 ± 0.09) vs. placebo (0.41 ± 0.05, P < 0.01), suggesting an increase in protein synthesis.

conclusionsFebuxostat attenuated cachexia progression and improved survival of tumour-bearing rats.

Indexed as

Cancer cachexiaSurvivalWastingWeight lossYoshida hepatoma animal model

Identifiers

PMID26136193
PMCPMC4458083
OpenAlexW2115797799

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.