Evidence map›Paper›PMID 27493872›Full record

ArticleJournal of cachexia, sarcopenia and muscle2016

White adipose tissue cells and the progression of cachexia: inflammatory pathways.

Rodrigo X Neves, José Cesar Rosa-Neto, Alex S Yamashita, Emidio M Matos-Neto, Daniela M R Riccardi, Fabio S Lira, Miguel L Batista, Marília Seelaender

Open access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Cachexia causes time-dependent activation of the inflammasome in the liver.Journal of cachexia, sarcopenia and muscle · 2023
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  3. Review
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  11. Adipogenesis in Different Body Depots and Tumor Development.Frontiers in cell and developmental biology · 2020
    Review
  12. Metastasis and cachexia: alongside in clinics, but not so in animal models.Journal of cachexia, sarcopenia and muscle · 2019
    Review
  13. Article
  14. Review
  15. Article
  16. Pseudomonas aeruginosa-derived pyocyanin reduces adipocyte differentiation, body weight, and fat mass as mechanisms contributing to septic cachexia.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2019
    Article
  17. Article
  18. Article
  19. Chemotherapy-induced muscle wasting: an update.European journal of translational myology · 2018
    Article
  20. 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

8 authors at 4 institutions in 2 countries.

Rodrigo X NevesCancer Metabolism Research Group.
José Cesar Rosa-NetoImmunometabolism Research Group.
Alex S YamashitaDepartment of Physiology and Biophysics, Institute of Biomedical Sciences University of São Paulo São Paulo Brazil.
Emidio M Matos-NetoCancer Metabolism Research Group.
Daniela M R RiccardiCancer Metabolism Research Group.
Fabio S LiraDepartment of Physical Education São Paulo State University, UNESP, Presidente Prudente Brazil.
Miguel L BatistaLaboratory of Adipose Tissue Biology, Center for Integrated Biotechnology University of Mogi das Cruzes Mogi das Cruzes Brazil.
Marília SeelaenderCancer Metabolism Research Group.
Immunome (United States) · USUniversidade de Mogi das Cruzes · BRUniversidade de São Paulo · BRUniversidade Estadual Paulista (Unesp) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCachexia is a systemic syndrome leading to body wasting, systemic inflammation, and to metabolic chaos. It is a progressive condition, and little is known about its dynamics. Detection of the early signs of the disease may lead to the attenuation of the associated symptoms. The white adipose tissue is an organ with endocrine functions, capable of synthesising and secreting a plethora of proteins, including cytokines, chemokines, and adipokines. It is well established that different adipose tissue depots demonstrate heterogeneous responses to physiological and pathological stimuli. The present study aimed at providing insight into adipocyte involvement in inflammation along the progression of cachexia.

methodsEight-weeks-old male rats were subcutaneously inoculated with a Walker 256 carcinosarcoma cell suspension (2 × 10(7) cells in 1.0 mL; tumour-bearing, T) or Phosphate-buffered saline (control, C). The retroperitoneal, epididymal, and mesenteric adipose pads were excised on Days 0, 7, and 14 post-tumour cell injection, and the adipocytes were isolated.

resultsMesenteric and epididymal adipocytes showed up-regulation of IL-1β protein expression and activation of the inflammasome pathway, contributing for whole tissue inflammation. The stromal vascular fraction of the retroperitoneal adipose tissue, on the other hand, seems to be the major contributor for the inflammation in this specific pad.

conclusionAdipocytes seem to play a relevant role in the establishment of white adipose tissue inflammation, through the activation of the NF-κB and inflammasome pathways. In epididymal adipocytes, induction of the inflammasome may be detected already on Day 7 post-tumour cell inoculation.

Indexed as

AdipocyteCancer cachexiaInflammasomeInflammation

Identifiers

PMID27493872
PMCPMC4864177
OpenAlexW1901479343

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.