Evidence map›Paper›PMID 29641213›Full record

ArticleAmerican journal of physiology. Cell physiology2018

Systemic IL-6 regulation of eccentric contraction-induced muscle protein synthesis.

Justin P Hardee, Dennis K Fix, Xuewen Wang, Edie C Goldsmith, Ho-Jin Koh, James A Carson

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Androgens as the "old age stick" in skeletal muscle.Cell communication and signaling : CCS · 2025
    Review
  5. Cancer Cachexia.Advances in experimental medicine and biology · 2025
    Review
  6. Review
  7. Exploring heterogeneity: a dive into preclinical models of cancer cachexia.American journal of physiology. Cell physiology · 2024
    Review
  8. Review
  9. Review
  10. Review
  11. Muscular contraction's therapeutic potential for cancer-induced wasting.American journal of physiology. Cell physiology · 2022
    Review
  12. CORP: Gene delivery into murine skeletal muscle using in vivo electroporation.Journal of applied physiology (Bethesda, Md. : 1985) · 2022
    Review
  13. Article
  14. Article
  15. Exercise as a therapy for cancer-induced muscle wasting.Sports medicine and health science · 2020
    Review
  16. Article
  17. Review
  18. Article
  19. 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

6 authors at 1 institution in 1 country.

Justin P HardeeDepartment of Exercise Science, University of South Carolina , Columbia, South Carolina.ORCID 0000-0001-6469-9592
Dennis K FixDepartment of Exercise Science, University of South Carolina , Columbia, South Carolina.
Xuewen WangDepartment of Exercise Science, University of South Carolina , Columbia, South Carolina.
Edie C GoldsmithDepartment of Cell Biology and Anatomy, University of South Carolina School of Medicine , Columbia, South Carolina.
Ho-Jin KohDepartment of Exercise Science, University of South Carolina , Columbia, South Carolina.ORCID 0000-0001-5922-0938
James A CarsonDepartment of Exercise Science, University of South Carolina , Columbia, South Carolina.
University of South Carolina · US

Funding

TISSUE BIOREPOSITORYP20RR017698 · NCRR · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI FAYAD, RAJA · 2002 to 2011
$22.5M
Cachexia in ApcMin/+ mice: The role of IL-6R01CA121249 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CARSON, JAMES A · 2008 to 2018
$2.7M
NCI NIH HHS R01 CA121249NCRR NIH HHS P20 RR017698
6 · The paper itself

Abstract

Systemic cytokines and contractile activity are established regulators of muscle protein turnover. Paradoxically, the IL-6 cytokine family, which shares the ubiquitously expressed membrane gp130 receptor, has been implicated in skeletal muscle's response to both contractions and cancer-induced wasting. Although we have reported that tumor-derived cachectic factors could suppress stretch-induced protein synthesis in cultured myotubes, the ability of systemic cytokines to disrupt in vivo eccentric contraction-induced protein synthesis has not been established. Therefore, we examined whether systemic IL-6 regulates basal and eccentric contraction-induced protein synthesis through muscle gp130 signaling. Systemic IL-6 overexpression was performed for 2 wk, and we then examined basal and eccentric contraction-induced protein synthesis and mammalian target of rapamycin complex 1 (mTORC1) signaling in tibialis anterior muscle of male wild-type, muscle-specific gp130 receptor knockout, and tumor-bearing Apc

Indexed as

AnimalsCachexiaInterleukin-6MaleMechanistic Target of Rapamycin Complex 1MiceMice, Inbred C57BLMuscle CellsMuscle ContractionMuscle Fibers, SkeletalMuscle ProteinsMuscle, SkeletalProtein BiosynthesisSignal TransductionInterleukin-6interleukin-6, mouseMechanistic Target of Rapamycin Complex 1Muscle Proteinscancer cachexiaeccentric contractionsinterleukin-6, muscle protein synthesis

Identifiers

PMID29641213
PMCPMC6087730
OpenAlexW2797576439

What OpenQuestion holds

Textmetadata
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.